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[ CAS No. 610-02-6 ] {[proInfo.proName]}

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Chemical Structure| 610-02-6
Chemical Structure| 610-02-6
Structure of 610-02-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 610-02-6 ]

CAS No. :610-02-6 MDL No. :MFCD00002447
Formula : C7H6O5 Boiling Point : -
Linear Structure Formula :- InChI Key :BRRSNXCXLSVPFC-UHFFFAOYSA-N
M.W : 170.12 Pubchem ID :11874
Synonyms :

Calculated chemistry of [ 610-02-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 5.0
Num. H-bond donors : 4.0
Molar Refractivity : 39.47
TPSA : 97.99 ?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 : Yes
Log Kp (skin permeation) : -6.59 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.93
Log Po/w (XLOGP3) : 1.05
Log Po/w (WLOGP) : 0.5
Log Po/w (MLOGP) : -0.16
Log Po/w (SILICOS-IT) : -0.2
Consensus Log Po/w : 0.42

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.86
Solubility : 2.35 mg/ml ; 0.0138 mol/l
Class : Very soluble
Log S (Ali) : -2.7
Solubility : 0.341 mg/ml ; 0.002 mol/l
Class : Soluble
Log S (SILICOS-IT) : -0.04
Solubility : 155.0 mg/ml ; 0.91 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 1.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.36

Safety of [ 610-02-6 ]

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 [ 610-02-6 ]

* 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 [ 610-02-6 ]

[ 610-02-6 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 610-02-6 ]
  • [ 77-78-1 ]
  • [ 5653-46-3 ]
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 12, p. 3319 - 3322
[2] Journal of the Chemical Society, 1938, p. 1602,1605
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