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 0 Sign in  

[ CAS No. 2162-98-3 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 2162-98-3
Chemical Structure| 2162-98-3
Structure of 2162-98-3 * Storage: {[proInfo.prStorage]}

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

Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Search after Editing

* Storage: {[proInfo.prStorage]}

* Shipping: {[proInfo.prShipping]}

Quality Control of [ 2162-98-3 ]

Related Doc. of [ 2162-98-3 ]

Alternatived Products of [ 2162-98-3 ]
Product Citations

Product Details of [ 2162-98-3 ]

CAS No. :2162-98-3 MDL No. :MFCD00000957
Formula : C10H20Cl2 Boiling Point : -
Linear Structure Formula :- InChI Key :RBBNTRDPSVZESY-UHFFFAOYSA-N
M.W : 211.17 Pubchem ID :75101
Synonyms :
Chemical Name :1,10-Dichlorodecane

Calculated chemistry of [ 2162-98-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 9
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 59.78
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.04 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.37
Log Po/w (XLOGP3) : 5.0
Log Po/w (WLOGP) : 4.58
Log Po/w (MLOGP) : 4.48
Log Po/w (SILICOS-IT) : 4.72
Consensus Log Po/w : 4.43

Druglikeness

Lipinski : 1.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.71
Solubility : 0.0416 mg/ml ; 0.000197 mol/l
Class : Soluble
Log S (Ali) : -4.74
Solubility : 0.00385 mg/ml ; 0.0000182 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -5.17
Solubility : 0.00144 mg/ml ; 0.00000682 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 3.0
Synthetic accessibility : 2.48

Safety of [ 2162-98-3 ]

Signal Word:Danger Class:9
Precautionary Statements:P280-P301+P312+P330-P305+P351+P338+P310 UN#:3082
Hazard Statements:H302-H315-H318-H410 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2162-98-3 ]

* 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 [ 2162-98-3 ]

[ 2162-98-3 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 18528-78-4 ]
  • [ 2162-98-3 ]
  • N,N′-(decane-1,10-diyl)bis(9-amino-2,3-dihydro-1H-cyclopenta[b]quinolinium)dichloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
4.5% In sulfolane; at 190 - 200℃; for 90.0h; A mixture of <strong>[18528-78-4]2,3-dihydro-1H-cyclopenta[b]quinolin-9-ylamine</strong> (0.45 g, 2.44 mmol), 1,10-dichlorodecane (0.25 g, 1.2mmol), and sulfolane (2 mL) was heated at 190-200 C for 90 h. The resulting mass was stirred with methanol and filtered. The filtrate was concentrated and chromatographedon an Al2O3 column using a gradient from 1 to 25% ofmethanol in methylene chloride. Fractions containing required product were pooled together and evaporated, andthe resulting off-white solid (31 mg, 4.5%) was further purified by crystallization from a methanol/acetone mixture [Mp 250-258 C (dec). 1H NMR (500 MHz, CDCl3) δ1.27-1.43 (m, 12 H), 1.67-1.76 (m, 4 H), 2.20-2.26 (m, 4H), 2.95 (t, 4 H, J = 7.5 Hz), 3.38 (t, 4 H, J = 7.5 Hz), 3.63(t, 4 H, J = 7.0 Hz), 4.46 (t, 4 H, J = 6.5 Hz),7.72 (t, 2 H, J = 7.0 Hz), 7.98 (t, 2 H, J = 7.5 Hz),8.15 (d, 2 H, J = 9.0 Hz), 8.54 (d with fine splitting, 2 H,J = 8.5 Hz), 8.92 (br s, 4 H, NH2).
In sulfolane; at 190 - 200℃; for 10.0h; General procedure: General methods for the synthesis of CABs are reported in Sharma et al. 2018 (Supra) and summarized in FIG. 5. Methods described in FIG. 5 are a) Amyl alcohol, reflux under N2, 12 h; b) No solvent, 180-195 C, 2 h; c) sulfolane, 190-200 C, 10 h. Three new CABs e.g. APDE-8, CODE-9 and CYDE-21 were successfully synthesized using the methods shown in FIG. 5.
Recommend Products
Same Skeleton Products

Technical Information

Historical Records

Related Functional Groups of
[ 2162-98-3 ]

Aliphatic Chain Hydrocarbons

Chemical Structure| 3386-33-2

[ 3386-33-2 ]

1-Chlorooctadecane

Similarity: 1.00

Chemical Structure| 821-99-8

[ 821-99-8 ]

1,9-Dichlorononane

Similarity: 1.00

Chemical Structure| 2163-00-0

[ 2163-00-0 ]

1,6-Dichlorohexane

Similarity: 1.00

Chemical Structure| 872-06-0

[ 872-06-0 ]

9-Chloronon-1-ene

Similarity: 0.77

Chemical Structure| 871-90-9

[ 871-90-9 ]

8-Chlorooct-1-ene

Similarity: 0.77

Chlorides

Chemical Structure| 3386-33-2

[ 3386-33-2 ]

1-Chlorooctadecane

Similarity: 1.00

Chemical Structure| 821-99-8

[ 821-99-8 ]

1,9-Dichlorononane

Similarity: 1.00

Chemical Structure| 2163-00-0

[ 2163-00-0 ]

1,6-Dichlorohexane

Similarity: 1.00

Chemical Structure| 872-06-0

[ 872-06-0 ]

9-Chloronon-1-ene

Similarity: 0.77

Chemical Structure| 871-90-9

[ 871-90-9 ]

8-Chlorooct-1-ene

Similarity: 0.77

; ;