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[ CAS No. 34317-61-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 34317-61-8
Chemical Structure| 34317-61-8
Structure of 34317-61-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 34317-61-8 ]

CAS No. :34317-61-8 MDL No. :MFCD01318758
Formula : C9H11NO2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :XYUBQWNJDIAEES-QMMMGPOBSA-N
M.W : 197.25 Pubchem ID :119462
Synonyms :
Chemical Name :(R)-2-Amino-3-(phenylthio)propanoic acid

Calculated chemistry of [ 34317-61-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 52.26
TPSA : 88.62 ?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) : -8.33 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.48
Log Po/w (XLOGP3) : -1.16
Log Po/w (WLOGP) : 1.19
Log Po/w (MLOGP) : -0.85
Log Po/w (SILICOS-IT) : 0.97
Consensus Log Po/w : 0.33

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.41
Solubility : 76.8 mg/ml ; 0.389 mol/l
Class : Very soluble
Log S (Ali) : -0.21
Solubility : 122.0 mg/ml ; 0.619 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.98
Solubility : 2.07 mg/ml ; 0.0105 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.57

Safety of [ 34317-61-8 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 34317-61-8 ]

* 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.

  • Upstream synthesis route of [ 34317-61-8 ]

[ 34317-61-8 ] Synthesis Path-Upstream   1~12

  • 1
  • [ 56-45-1 ]
  • [ 108-98-5 ]
  • [ 34317-61-8 ]
Reference: [1] Journal of the American Chemical Society, 1993, vol. 115, # 4, p. 1264 - 1270
  • 2
  • [ 88347-90-4 ]
  • [ 34317-61-8 ]
Reference: [1] Organic Letters, 2012, vol. 14, # 1, p. 334 - 337
  • 3
  • [ 2731-73-9 ]
  • [ 108-98-5 ]
  • [ 34317-61-8 ]
Reference: [1] Patent: US6372941, 2002, B1, . Location in patent: Page column 20
[2] Agricultural and Biological Chemistry, 1989, vol. 53, # 9, p. 2481 - 2487
  • 4
  • [ 108-98-5 ]
  • [ 34317-61-8 ]
Reference: [1] Organic Letters, 2012, vol. 14, # 1, p. 334 - 337
  • 5
  • [ 52-90-4 ]
  • [ 1483-72-3 ]
  • [ 34317-61-8 ]
Reference: [1] Journal of the American Chemical Society, 1947, vol. 69, p. 1550
  • 6
  • [ 121704-26-5 ]
  • [ 34317-61-8 ]
  • [ 121704-26-5 ]
Reference: [1] Journal of the American Chemical Society, 1989, vol. 111, # 16, p. 6354 - 6364
  • 7
  • [ 407-41-0 ]
  • [ 108-98-5 ]
  • [ 34317-61-8 ]
Reference: [1] Chemistry Letters, 2017, vol. 46, # 12, p. 1789 - 1792
  • 8
  • [ 68724-10-7 ]
  • [ 34317-61-8 ]
Reference: [1] Journal of Biological Chemistry, 1943, vol. 151, p. 211,212
  • 9
  • [ 52-90-4 ]
  • [ 34317-61-8 ]
Reference: [1] Biochemical Journal, 1951, vol. 48, p. 624,625
  • 10
  • [ 2684-02-8 ]
  • [ 52-90-4 ]
  • [ 34317-61-8 ]
Reference: [1] Journal of Biological Chemistry, 1943, vol. 151, p. 211,212
[2] Journal of Biological Chemistry, 1931, vol. 94, p. 541,544
[3] Journal of Biological Chemistry, 1931, vol. 94, p. 541,544
  • 11
  • [ 108-98-5 ]
  • [ 1758-77-6 ]
  • [ 34317-61-8 ]
  • [ 114502-04-4 ]
Reference: [1] Tetrahedron, 1987, vol. 43, # 17, p. 3881 - 3888
  • 12
  • [ 52-90-4 ]
  • [ 1483-72-3 ]
  • [ 7732-18-5 ]
  • [ 34317-61-8 ]
Reference: [1] Journal of the American Chemical Society, 1947, vol. 69, p. 1550
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