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[ CAS No. 1004-96-2 ] {[proInfo.proName]}

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Chemical Structure| 1004-96-2
Chemical Structure| 1004-96-2
Structure of 1004-96-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1004-96-2 ]

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Product Details of [ 1004-96-2 ]

CAS No. :1004-96-2 MDL No. :MFCD10699057
Formula : C6H7NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :MBRNUSBFRMCWIZ-UHFFFAOYSA-N
M.W : 141.12 Pubchem ID :70492
Synonyms :

Calculated chemistry of [ 1004-96-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.33
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 32.75
TPSA : 52.33 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.48 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.78
Log Po/w (XLOGP3) : 0.96
Log Po/w (WLOGP) : 0.77
Log Po/w (MLOGP) : -0.02
Log Po/w (SILICOS-IT) : 1.08
Consensus Log Po/w : 0.91

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.56
Solubility : 3.91 mg/ml ; 0.0277 mol/l
Class : Very soluble
Log S (Ali) : -1.65
Solubility : 3.19 mg/ml ; 0.0226 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.68
Solubility : 2.98 mg/ml ; 0.0211 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.36

Safety of [ 1004-96-2 ]

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

Application In Synthesis of [ 1004-96-2 ]

* 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.

  • Downstream synthetic route of [ 1004-96-2 ]

[ 1004-96-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 67-56-1 ]
  • [ 4857-42-5 ]
  • [ 1004-96-2 ]
YieldReaction ConditionsOperation in experiment
76% With thionyl chloride; at 0 - 40℃; for 3.25h; To a solution of compound 9 (1 g, 7.9 mmoi, 1.0 eq) in dry MeOH (20 mi.) was added SOCI2 (1 g, 8,7 mmol, 1.1 eq) slowly at 0 °C. The reaction mixture was stirred at 25 °C for 15 min and heated to 40 °C for 3 h. The reaction mixture was concentrated under reduced pressure, dissolved in EtOAc (50 mL), washed with brine (2 x 50 mL), dried over anhydrous Na2SOa, filtered and concentrated in vacuum. The residue was purified by column chromatography (0-20percent EtOAc in PE) to afford 10 (850 mg, 6.0 mmol, 76percent yield) as a white solid: JH NM (400 M Hz, CDCI3) delta 2.40 (s, 3H), 3.98 (s, 3H), 6.82 (s, 1H).
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