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[ CAS No. 19771-63-2 ] {[proInfo.proName]}

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Chemical Structure| 19771-63-2
Chemical Structure| 19771-63-2
Structure of 19771-63-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 19771-63-2 ]

CAS No. :19771-63-2 MDL No. :MFCD00066092
Formula : C4H5NO3S Boiling Point : -
Linear Structure Formula :(C3H4NS(O))COOH InChI Key :BMLMGCPTLHPWPY-REOHCLBHSA-N
M.W : 147.15 Pubchem ID :72390
Synonyms :
Oxothiazolidinecarboxylic acid;L-2-oxothiazolidine-4-Carboxylate;OTC;L-2-oxothiazolidine-4-Carboxylic Acid
Chemical Name :(R)-2-Oxothiazolidine-4-carboxylic acid

Calculated chemistry of [ 19771-63-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.5
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 35.9
TPSA : 91.7 ?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) : -7.28 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.38
Log Po/w (XLOGP3) : -0.11
Log Po/w (WLOGP) : -0.48
Log Po/w (MLOGP) : -0.93
Log Po/w (SILICOS-IT) : 0.05
Consensus Log Po/w : -0.22

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -0.62
Solubility : 35.5 mg/ml ; 0.242 mol/l
Class : Very soluble
Log S (Ali) : -1.36
Solubility : 6.38 mg/ml ; 0.0434 mol/l
Class : Very soluble
Log S (SILICOS-IT) : 0.12
Solubility : 192.0 mg/ml ; 1.31 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.06

Safety of [ 19771-63-2 ]

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 [ 19771-63-2 ]

* 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 [ 19771-63-2 ]
  • Downstream synthetic route of [ 19771-63-2 ]

[ 19771-63-2 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 52-89-1 ]
  • [ 1885-14-9 ]
  • [ 19771-63-2 ]
Reference: [1] Chemistry - A European Journal, 2004, vol. 10, # 23, p. 6102 - 6110
[2] Patent: EP1462444, 2004, A1, . Location in patent: Page 23
[3] European Journal of Pharmaceutics and Biopharmaceutics, 2016, vol. 103, p. 62 - 70
  • 2
  • [ 52-90-4 ]
  • [ 32315-10-9 ]
  • [ 19771-63-2 ]
Reference: [1] Synthetic Communications, 1993, vol. 23, # 20, p. 2839 - 2844
[2] Patent: US10239847, 2019, B1, . Location in patent: Page/Page column 9; 10
  • 3
  • [ 75-44-5 ]
  • [ 52-90-4 ]
  • [ 19771-63-2 ]
Reference: [1] Bulletin of the Chemical Society of Japan, 1964, vol. 37, # 2, p. 242 - 244
  • 4
  • [ 127761-77-7 ]
  • [ 19771-63-2 ]
Reference: [1] Journal of Organic Chemistry, 1992, vol. 57, # 20, p. 5292 - 5300
  • 5
  • [ 52-90-4 ]
  • [ 19771-63-2 ]
Reference: [1] Patent: EP1462444, 2004, A1, . Location in patent: Page 12
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