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[ CAS No. 532-03-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 532-03-6
Chemical Structure| 532-03-6
Structure of 532-03-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 532-03-6 ]

CAS No. :532-03-6 MDL No. :MFCD00057662
Formula : C11H15NO5 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 241.24 Pubchem ID :-
Synonyms :
AHR 85;NSC 170960;Whitehall Robins Brand of Methocarbamol;Shire Brand of Methocarbamol;Schwarz Brand of Methocarbamol;Metocarbamol;Metocarbamolo;Lumirelax;Robaxin;Guaiphenesin Carbamate;Guaiacol Glyceryl Ether Carbamate

Calculated chemistry of [ 532-03-6 ]

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.36
Num. rotatable bonds : 7
Num. H-bond acceptors : 5.0
Num. H-bond donors : 2.0
Molar Refractivity : 59.39
TPSA : 91.01 Ų

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) : -7.34 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.92
Log Po/w (XLOGP3) : 0.61
Log Po/w (WLOGP) : 0.53
Log Po/w (MLOGP) : 0.15
Log Po/w (SILICOS-IT) : 0.41
Consensus Log Po/w : 0.72

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.52
Solubility : 7.3 mg/ml ; 0.0303 mol/l
Class : Very soluble
Log S (Ali) : -2.1
Solubility : 1.94 mg/ml ; 0.00803 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.89
Solubility : 3.14 mg/ml ; 0.013 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.63

Safety of [ 532-03-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338-P310 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 532-03-6 ]

* 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.

  • Upstream synthesis route of [ 532-03-6 ]
  • Downstream synthetic route of [ 532-03-6 ]

[ 532-03-6 ] Synthesis Path-Upstream   1~10

  • 1
  • [ 93950-95-9 ]
  • [ 532-03-6 ]
Reference: [1] Monatshefte fuer Chemie, 1963, vol. 94, p. 339 - 358
[2] Monatshefte fuer Chemie, 1963, vol. 94, p. 339 - 358
  • 2
  • [ 93728-27-9 ]
  • [ 532-03-6 ]
Reference: [1] Monatshefte fuer Chemie, 1963, vol. 94, p. 339 - 358
[2] Monatshefte fuer Chemie, 1963, vol. 94, p. 339 - 358
  • 3
  • [ 94997-48-5 ]
  • [ 532-03-6 ]
Reference: [1] Monatshefte fuer Chemie, 1963, vol. 94, p. 339 - 358
  • 4
  • [ 94824-19-8 ]
  • [ 532-03-6 ]
Reference: [1] Monatshefte fuer Chemie, 1963, vol. 94, p. 339 - 358
  • 5
  • [ 10488-39-8 ]
  • [ 532-03-6 ]
Reference: [1] Monatshefte fuer Chemie, 1963, vol. 94, p. 339 - 358
[2] Monatshefte fuer Chemie, 1963, vol. 94, p. 339 - 358
  • 6
  • [ 92042-73-4 ]
  • [ 532-03-6 ]
Reference: [1] Monatshefte fuer Chemie, 1963, vol. 94, p. 339 - 358
[2] Monatshefte fuer Chemie, 1963, vol. 94, p. 339 - 358
  • 7
  • [ 2049-22-1 ]
  • [ 532-03-6 ]
Reference: [1] Monatshefte fuer Chemie, 1963, vol. 94, p. 339 - 358
[2] Monatshefte fuer Chemie, 1963, vol. 94, p. 339 - 358
  • 8
  • [ 2049-21-0 ]
  • [ 7664-41-7 ]
  • [ 67-63-0 ]
  • [ 532-03-6 ]
  • [ 10488-39-8 ]
Reference: [1] Journal of Organic Chemistry, 1957, vol. 22, p. 1595,1598
  • 9
  • [ 532-03-6 ]
  • [ 93-14-1 ]
Reference: [1] Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 2014, vol. 128, p. 263 - 271
  • 10
  • [ 532-03-6 ]
  • [ 10488-39-8 ]
  • [ 93-14-1 ]
Reference: [1] Journal of Pharmaceutical Sciences, 1994, vol. 83, # 4, p. 499 - 501
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