成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

Home Cart Sign in  
HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 127946-77-4 Chemical Structure| 127946-77-4
Chemical Structure| 127946-77-4

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

{[proInfo.proName]}

CAS No.: 127946-77-4

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support Online Technical Q&A
Product Citations

Alternative Products

Product Details of [ 127946-77-4 ]

CAS No. :127946-77-4
Formula : C4H7ClN2
M.W : 118.57
SMILES Code : Cl.NC1(CC1)C#N
MDL No. :MFCD04114063
InChI Key :PCEIEQLJYDMRFZ-UHFFFAOYSA-N
Pubchem ID :14586363

Safety of [ 127946-77-4 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H317-H319
Precautionary Statements:P280-P301+P310-P305+P351+P338
Class:6.1
UN#:3439
Packing Group:Ⅲ

Calculated chemistry of [ 127946-77-4 ] Show Less

Physicochemical Properties

Num. heavy atoms 7
Num. arom. heavy atoms 0
Fraction Csp3 0.75
Num. rotatable bonds 0
Num. H-bond acceptors 2.0
Num. H-bond donors 1.0
Molar Refractivity 28.69
TPSA ?

Topological Polar Surface Area: Calculated from
Ertl P. et al. 2000 J. Med. Chem.

49.81 ?2

Lipophilicity

Log Po/w (iLOGP)?

iLOGP: in-house physics-based method implemented from
Daina A et al. 2014 J. Chem. Inf. Model.

0.0
Log Po/w (XLOGP3)?

XLOGP3: Atomistic and knowledge-based method calculated by
XLOGP program, version 3.2.2, courtesy of CCBG, Shanghai Institute of Organic Chemistry

0.22
Log Po/w (WLOGP)?

WLOGP: Atomistic method implemented from
Wildman SA and Crippen GM. 1999 J. Chem. Inf. Model.

0.74
Log Po/w (MLOGP)?

MLOGP: Topological method implemented from
Moriguchi I. et al. 1992 Chem. Pharm. Bull.
Moriguchi I. et al. 1994 Chem. Pharm. Bull.
Lipinski PA. et al. 2001 Adv. Drug. Deliv. Rev.

-0.31
Log Po/w (SILICOS-IT)?

SILICOS-IT: Hybrid fragmental/topological method calculated by
FILTER-IT program, version 1.0.2, courtesy of SILICOS-IT, http://www.silicos-it.com

0.33
Consensus Log Po/w?

Consensus Log Po/w: Average of all five predictions

0.2

Water Solubility

Log S (ESOL):?

ESOL: Topological method implemented from
Delaney JS. 2004 J. Chem. Inf. Model.

-0.71
Solubility 22.9 mg/ml ; 0.193 mol/l
Class?

Solubility class: Log S scale
Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly

Very soluble
Log S (Ali)?

Ali: Topological method implemented from
Ali J. et al. 2012 J. Chem. Inf. Model.

-0.83
Solubility 17.7 mg/ml ; 0.149 mol/l
Class?

Solubility class: Log S scale
Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly

Very soluble
Log S (SILICOS-IT)?

SILICOS-IT: Fragmental method calculated by
FILTER-IT program, version 1.0.2, courtesy of SILICOS-IT, http://www.silicos-it.com

-0.31
Solubility 57.9 mg/ml ; 0.489 mol/l
Class?

Solubility class: Log S scale
Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly

Soluble

Pharmacokinetics

GI absorption?

Gatrointestinal absorption: according to the white of the BOILED-Egg

 High
BBB permeant?

BBB permeation: according to the yolk of the BOILED-Egg

 Yes
P-gp substrate?

P-glycoprotein substrate: SVM model built on 1033 molecules (training set)
and tested on 415 molecules (test set)
10-fold CV: ACC=0.72 / AUC=0.77
External: ACC=0.88 / AUC=0.94

 No
CYP1A2 inhibitor?

Cytochrome P450 1A2 inhibitor: SVM model built on 9145 molecules (training set)
and tested on 3000 molecules (test set)
10-fold CV: ACC=0.83 / AUC=0.90
External: ACC=0.84 / AUC=0.91

 No
CYP2C19 inhibitor?

Cytochrome P450 2C19 inhibitor: SVM model built on 9272 molecules (training set)
and tested on 3000 molecules (test set)
10-fold CV: ACC=0.80 / AUC=0.86
External: ACC=0.80 / AUC=0.87

 No
CYP2C9 inhibitor?

Cytochrome P450 2C9 inhibitor: SVM model built on 5940 molecules (training set)
and tested on 2075 molecules (test set)
10-fold CV: ACC=0.78 / AUC=0.85
External: ACC=0.71 / AUC=0.81

 No
CYP2D6 inhibitor?

Cytochrome P450 2D6 inhibitor: SVM model built on 3664 molecules (training set)
and tested on 1068 molecules (test set)
10-fold CV: ACC=0.79 / AUC=0.85
External: ACC=0.81 / AUC=0.87

 No
CYP3A4 inhibitor?

Cytochrome P450 3A4 inhibitor: SVM model built on 7518 molecules (training set)
and tested on 2579 molecules (test set)
10-fold CV: ACC=0.77 / AUC=0.85
External: ACC=0.78 / AUC=0.86

 Yes
Log Kp (skin permeation)?

Skin permeation: QSPR model implemented from
Potts RO and Guy RH. 1992 Pharm. Res.

-6.87 cm/s

Druglikeness

Lipinski?

Lipinski (Pfizer) filter: implemented from
Lipinski CA. et al. 2001 Adv. Drug Deliv. Rev.
MW ≤ 500
MLOGP ≤ 4.15
N or O ≤ 10
NH or OH ≤ 5

 0.0
Ghose?

Ghose filter: implemented from
Ghose AK. et al. 1999 J. Comb. Chem.
160 ≤ MW ≤ 480
-0.4 ≤ WLOGP ≤ 5.6
40 ≤ MR ≤ 130
20 ≤ atoms ≤ 70

 None
Veber?

Veber (GSK) filter: implemented from
Veber DF. et al. 2002 J. Med. Chem.
Rotatable bonds ≤ 10
TPSA ≤ 140

 0.0
Egan?

Egan (Pharmacia) filter: implemented from
Egan WJ. et al. 2000 J. Med. Chem.
WLOGP ≤ 5.88
TPSA ≤ 131.6

 0.0
Muegge?

Muegge (Bayer) filter: implemented from
Muegge I. et al. 2001 J. Med. Chem.
200 ≤ MW ≤ 600
-2 ≤ XLOGP ≤ 5
TPSA ≤ 150
Num. rings ≤ 7
Num. carbon > 4
Num. heteroatoms > 1
Num. rotatable bonds ≤ 15
H-bond acc. ≤ 10
H-bond don. ≤ 5

 2.0
Bioavailability Score?

Abbott Bioavailability Score: Probability of F > 10% in rat
implemented from
Martin YC. 2005 J. Med. Chem.

0.55

Medicinal Chemistry

PAINS?

Pan Assay Interference Structures: implemented from
Baell JB. & Holloway GA. 2010 J. Med. Chem.

0.0 alert
Brenk?

Structural Alert: implemented from
Brenk R. et al. 2008 ChemMedChem

0.0 alert: heavy_metal
Leadlikeness?

Leadlikeness: implemented from
Teague SJ. 1999 Angew. Chem. Int. Ed.
250 ≤ MW ≤ 350
XLOGP ≤ 3.5
Num. rotatable bonds ≤ 7

 No; 1 violation:MW<1.0
Synthetic accessibility?

Synthetic accessibility score: from 1 (very easy) to 10 (very difficult)
based on 1024 fragmental contributions (FP2) modulated by size and complexity penaties,
trained on 12'782'590 molecules and tested on 40 external molecules (r2 = 0.94)

 1.47

Application In Synthesis of [ 127946-77-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 127946-77-4 ]

[ 127946-77-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 85-42-7 ]
  • [ 114041-16-6 ]
  • [ 127946-77-4 ]
  • [ 1403499-41-1 ]
  • 2
  • [ 187669-60-9 ]
  • [ 85-42-7 ]
  • [ 127946-77-4 ]
  • [ 1095534-28-3 ]
  • 3
  • [ 97914-59-5 ]
  • [ 127946-77-4 ]
  • N-(1-cyanocyclopropyl)-2-(difluoromethoxy)benzamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
42% With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; at 0 - 20℃; for 12h; To a stirred solution of 2-(difluoro methoxy)benzoic acid (1g, 5.32 mmol) and 1- aminocyclopropane-1-carbonitrile hydrochloride (747 mg, 6.40 mmol) in DMF (20 mL) at 0oC were added TEA (3.0 mL, 21.28 mmol), EDC.HCl (1.52 mg, 7.98 mmol) and HOBt (1.07 mg, 7.98 mmol). Then the resulting reaction mixture was stirred at room temperature for 12h. After the completion of reaction, the mixture was diluted with ice cold water and extracted with EtOAc. The combined organic layers was washed with ice cold water (3 x 100 mL), brine (2 x 100mL) and dried over Na2SO4. Concentration followed by the purification of the crude product using flash column chromatography to afford N-(1- cyanocyclopropyl)-2-(difluoro methoxy)benzamide (560 mg, yield: 42 %) as an off-white solid.1H NMR (400 MHz, DMSO): δ 9.20 (s, 1H), 7.51-7.56 (m, 2H), 6.94-7.34 (m, 3H), 1.53-1.57 (m, 2H), 1.18-1.22(m, 2H). LC-MS (ESI): m/z 400.1 (M+H) +
 

Related Products

Historical Records

Technical Information

Categories

Related Functional Groups of
[ 127946-77-4 ]

Aliphatic Cyclic Hydrocarbons

Chemical Structure| 160133-27-7

A175049 [160133-27-7]

4-Aminobicyclo[2.2.2]octane-1-carbonitrile hydrochloride

Similarity: 0.69

Chemical Structure| 1303968-08-2

A173033 [1303968-08-2]

4-Aminocyclohexanecarbonitrile hydrochloride

Similarity: 0.68

Chemical Structure| 88887-87-0

A105931 [88887-87-0]

1-Methylcyclopropanamine hydrochloride

Similarity: 0.67

Chemical Structure| 1363405-41-7

A290175 [1363405-41-7]

2-(1-Aminocyclopentyl)acetonitrile hydrochloride

Similarity: 0.65

Chemical Structure| 1205544-78-0

A160068 [1205544-78-0]

1-(Aminomethyl)cyclopropanecarbonitrile hydrochloride

Similarity: 0.62

Amines

Chemical Structure| 4475-95-0

A109388 [4475-95-0]

2-Amino-2-methylbutanenitrile

Similarity: 0.86

Chemical Structure| 50846-36-1

A252211 [50846-36-1]

2-Amino-2-methylpropanenitrile hydrochloride

Similarity: 0.76

Chemical Structure| 160133-27-7

A175049 [160133-27-7]

4-Aminobicyclo[2.2.2]octane-1-carbonitrile hydrochloride

Similarity: 0.69

Chemical Structure| 1073666-54-2

A177970 [1073666-54-2]

(S)-3-Aminobutanenitrile hydrochloride

Similarity: 0.68

Chemical Structure| 1073666-55-3

A436181 [1073666-55-3]

(R)-3-Aminobutanenitrile hydrochloride

Similarity: 0.68

Nitriles

Chemical Structure| 4475-95-0

A109388 [4475-95-0]

2-Amino-2-methylbutanenitrile

Similarity: 0.86

Chemical Structure| 50846-36-1

A252211 [50846-36-1]

2-Amino-2-methylpropanenitrile hydrochloride

Similarity: 0.76

Chemical Structure| 160133-27-7

A175049 [160133-27-7]

4-Aminobicyclo[2.2.2]octane-1-carbonitrile hydrochloride

Similarity: 0.69

Chemical Structure| 1073666-54-2

A177970 [1073666-54-2]

(S)-3-Aminobutanenitrile hydrochloride

Similarity: 0.68

Chemical Structure| 1073666-55-3

A436181 [1073666-55-3]

(R)-3-Aminobutanenitrile hydrochloride

Similarity: 0.68