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. 17407-56-6 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 17407-56-6
Chemical Structure| 17407-56-6
Structure of 17407-56-6 * 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 [ 17407-56-6 ]

Related Doc. of [ 17407-56-6 ]

Alternatived Products of [ 17407-56-6 ]
Product Citations

Product Details of [ 17407-56-6 ]

CAS No. :17407-56-6 MDL No. :MFCD00066442
Formula : C5H10O3 Boiling Point : -
Linear Structure Formula :- InChI Key :NGEWQZIDQIYUNV-SCSAIBSYSA-N
M.W : 118.13 Pubchem ID :5289545
Synonyms :

Calculated chemistry of [ 17407-56-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.8
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 29.08
TPSA : 57.53 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.67 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.93
Log Po/w (XLOGP3) : 0.5
Log Po/w (WLOGP) : 0.09
Log Po/w (MLOGP) : 0.01
Log Po/w (SILICOS-IT) : -0.3
Consensus Log Po/w : 0.25

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -0.76
Solubility : 20.7 mg/ml ; 0.176 mol/l
Class : Very soluble
Log S (Ali) : -1.28
Solubility : 6.23 mg/ml ; 0.0527 mol/l
Class : Very soluble
Log S (SILICOS-IT) : 0.5
Solubility : 374.0 mg/ml ; 3.17 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.46

Safety of [ 17407-56-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 17407-56-6 ]

* 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 [ 17407-56-6 ]

[ 17407-56-6 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 3715-29-5 ]
  • [ 17407-56-6 ]
  • 2
  • [ 17407-56-6 ]
  • [ 13850-91-4 ]
  • (R)-2-(tert-Butoxycarbonyl-methyl-amino)-3-methyl-butyric acid (R)-1-carboxy-2-methyl-propyl ester [ No CAS ]
  • 3
  • carriebowmide [ No CAS ]
  • [ 56-41-7 ]
  • [ 17407-56-6 ]
  • [ 3060-46-6 ]
  • [ 63-91-2 ]
  • [ 56564-52-4 ]
  • 4
  • [ 1342821-20-8 ]
  • [ 17407-56-6 ]
  • [ 2480-23-1 ]
  • [ 2566-30-5 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; water; at 110℃; for 15h; Compound 1 (1.5 mg) was hydrolyzed with 6 M HCl (0.5 mL) at 110 C for 15 h. After concentration to dryness, the residue was dissolved in MeOH (200 μL) and subjected to HPLC analysis. In the same manner, compound 2 was hydrolyzed. HPLC analysis of the depsipeptide hydrolysates was performed using a ligand-exchange-type chiral column: Phenomenex Chirex 3126 (d)-penicillamine, 4.6×250 mm; mobile phase 2-propanol in 2 mM aqueous CuSO4; flow rate 1 mL/min, UV 235 nm. The 2-hydroxyisovaleric acid standard was purchased from Aldrich. Two mobile phase conditions were employed due to the large retention time differences of the standard samples: (1) 15% 2-propanol in 2 mM aqueous CuSO4, N-Me-l-Val and N-Me-d-Val (tR 7.0 min, peaks were superimposed), N-Me-l-Phe (tR 26.6 min), N-Me-d-Phe (tR 30.8 min), l-Hiv (tR 40.0 min), and d-Hiv (tR 67.4 min); (2) 5% 2-propanol in 2 mM aqueous CuSO4, N-Me-l-Val (tR 11.0 min), N-Me-d-Val (tR 13.9 min). Hydrolyzates of 1 and 2 contained N-Me-l-Val, N-Me-l-Phe, and d-Hiv.
  • 5
  • [ 1342821-22-0 ]
  • [ 17407-56-6 ]
  • [ 2480-23-1 ]
  • [ 2566-30-5 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; water; at 110℃; for 15h; Compound 1 (1.5 mg) was hydrolyzed with 6 M HCl (0.5 mL) at 110 C for 15 h. After concentration to dryness, the residue was dissolved in MeOH (200 μL) and subjected to HPLC analysis. In the same manner, compound 2 was hydrolyzed. HPLC analysis of the depsipeptide hydrolysates was performed using a ligand-exchange-type chiral column: Phenomenex Chirex 3126 (d)-penicillamine, 4.6×250 mm; mobile phase 2-propanol in 2 mM aqueous CuSO4; flow rate 1 mL/min, UV 235 nm. The 2-hydroxyisovaleric acid standard was purchased from Aldrich. Two mobile phase conditions were employed due to the large retention time differences of the standard samples: (1) 15% 2-propanol in 2 mM aqueous CuSO4, N-Me-l-Val and N-Me-d-Val (tR 7.0 min, peaks were superimposed), N-Me-l-Phe (tR 26.6 min), N-Me-d-Phe (tR 30.8 min), l-Hiv (tR 40.0 min), and d-Hiv (tR 67.4 min); (2) 5% 2-propanol in 2 mM aqueous CuSO4, N-Me-l-Val (tR 11.0 min), N-Me-d-Val (tR 13.9 min). Hydrolyzates of 1 and 2 contained N-Me-l-Val, N-Me-l-Phe, and d-Hiv.
  • 6
  • [ 1342309-23-2 ]
  • [ 17407-56-6 ]
  • [ 17407-55-5 ]
  • [ 312-84-5 ]
  • [ 56-45-1 ]
  • [ 20312-37-2 ]
  • [ 13748-90-8 ]
  • [ 3060-46-6 ]
  • [ 63-91-2 ]
  • [ 31321-74-1 ]
  • [ 673-06-3 ]
  • 7
  • [ 1342309-24-3 ]
  • [ 17407-56-6 ]
  • [ 17407-55-5 ]
  • [ 312-84-5 ]
  • [ 56-45-1 ]
  • [ 20312-37-2 ]
  • [ 13748-90-8 ]
  • [ 3060-46-6 ]
  • [ 63-91-2 ]
  • [ 31321-74-1 ]
  • [ 673-06-3 ]
  • 8
  • urumamide [ No CAS ]
  • [ 3913-67-5 ]
  • [ 72-18-4 ]
  • [ 17407-56-6 ]
  • [ 2480-23-1 ]
  • [ 61-90-5 ]
  • [ 3060-46-6 ]
  • [ 4125-98-8 ]
  • [ 147-85-3 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In water; at 110℃; for 24h; Urumamide (1) (0.7 mg) was treated with 9 N HCl (100 L) for 24 h at 110 C. The hydrolyzed product was evaporated to dryness and could be separated into each component by HPLC. [Cosmosil 5C18-PAQ (4.6 × 250 mm); flowrate, 1.0 mL/min; detection at 215 nm; solvent H2O. Retention times (min) of components: N-Me-Ala (tR = 3.0 min), Pro(tR = 3.2 min), Val (tR = 3.4 min), N-Me-Val (tR = 3.7 min), Leu (tR = 4.8 min), N-Me-Ile (tR = 5.3 min), N-Me-Leu (tR =6.0 min)].
Recommend Products
Same Skeleton Products

Technical Information

Historical Records

Related Functional Groups of
[ 17407-56-6 ]

Aliphatic Chain Hydrocarbons

Chemical Structure| 17407-55-5

[ 17407-55-5 ]

(S)-2-Hydroxy-3-methylbutanoic acid

Similarity: 1.00

Chemical Structure| 4026-18-0

[ 4026-18-0 ]

2-Hydroxy-3-methylbutanoic acid

Similarity: 1.00

Chemical Structure| 21641-92-9

[ 21641-92-9 ]

(S)-2-Hydroxy-3,3-dimethylbutanoic acid

Similarity: 0.96

Chemical Structure| 13748-90-8

[ 13748-90-8 ]

(S)-2-Hydroxy-4-methylpentanoic acid

Similarity: 0.92

Chemical Structure| 20312-37-2

[ 20312-37-2 ]

(R)-2-Hydroxy-4-methylpentanoic acid

Similarity: 0.92

Alcohols

Chemical Structure| 17407-55-5

[ 17407-55-5 ]

(S)-2-Hydroxy-3-methylbutanoic acid

Similarity: 1.00

Chemical Structure| 4026-18-0

[ 4026-18-0 ]

2-Hydroxy-3-methylbutanoic acid

Similarity: 1.00

Chemical Structure| 21641-92-9

[ 21641-92-9 ]

(S)-2-Hydroxy-3,3-dimethylbutanoic acid

Similarity: 0.96

Chemical Structure| 13748-90-8

[ 13748-90-8 ]

(S)-2-Hydroxy-4-methylpentanoic acid

Similarity: 0.92

Chemical Structure| 20312-37-2

[ 20312-37-2 ]

(R)-2-Hydroxy-4-methylpentanoic acid

Similarity: 0.92

Carboxylic Acids

Chemical Structure| 17407-55-5

[ 17407-55-5 ]

(S)-2-Hydroxy-3-methylbutanoic acid

Similarity: 1.00

Chemical Structure| 4026-18-0

[ 4026-18-0 ]

2-Hydroxy-3-methylbutanoic acid

Similarity: 1.00

Chemical Structure| 21641-92-9

[ 21641-92-9 ]

(S)-2-Hydroxy-3,3-dimethylbutanoic acid

Similarity: 0.96

Chemical Structure| 13748-90-8

[ 13748-90-8 ]

(S)-2-Hydroxy-4-methylpentanoic acid

Similarity: 0.92

Chemical Structure| 20312-37-2

[ 20312-37-2 ]

(R)-2-Hydroxy-4-methylpentanoic acid

Similarity: 0.92

; ;