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[ CAS No. 1038509-28-2 ] {[proInfo.proName]}

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Chemical Structure| 1038509-28-2
Chemical Structure| 1038509-28-2
Structure of 1038509-28-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1038509-28-2 ]

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Product Details of [ 1038509-28-2 ]

CAS No. :1038509-28-2 MDL No. :MFCD13190218
Formula : C9H7NO2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :SVEZOHPWBLWBNO-UHFFFAOYSA-N
M.W : 193.22 Pubchem ID :59316815
Synonyms :

Calculated chemistry of [ 1038509-28-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.11
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 50.9
TPSA : 67.43 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.9 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.11
Log Po/w (XLOGP3) : 2.23
Log Po/w (WLOGP) : 2.08
Log Po/w (MLOGP) : 1.35
Log Po/w (SILICOS-IT) : 2.96
Consensus Log Po/w : 2.15

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.82
Solubility : 0.29 mg/ml ; 0.0015 mol/l
Class : Soluble
Log S (Ali) : -3.28
Solubility : 0.101 mg/ml ; 0.000523 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.05
Solubility : 0.173 mg/ml ; 0.000893 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.11

Safety of [ 1038509-28-2 ]

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

Application In Synthesis of [ 1038509-28-2 ]

* 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 [ 1038509-28-2 ]

[ 1038509-28-2 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 209459-11-0 ]
  • [ 1038509-28-2 ]
YieldReaction ConditionsOperation in experiment
With isopentyl nitrite; In tetrahydrofuran; for 4h;Heating / reflux; Isoamyl nitrite (22.0 mmol) is added to a solution of 2-amino-benzothiazole-7-carboxylic acid methyl ester (10.1 mmol) in THF (29 mL). The mixture is heated to reflux for 4h, the solvents are removed in vacuo and the residue is purified by flash chromatography <n="80"/>(gradient: heptane to EtOAc/heptane 4/6) to give the desired product. LC-MS: tR = 0.85 min; [M+H]+ = 194.0.
With isopentyl nitrite; In tetrahydrofuran; for 4h;Heating / reflux; Isoamyl nitrite (22.0 mmol) is added to a solution of 2-amino-benzothiazole- 7-carboxylic acid methyl ester (10.1 mmol) in THF (29 mL). The mixture is heated to reflux for 4h, the solvents are removed in vacuo and the residue is purified by FC (gradient: heptane to EtO Ac/heptane 4/6) to give the desired product. LC-MS: tR = 0.85 min; [M+H]+ = 194.0.
With isopentyl nitrite; In tetrahydrofuran; for 4h;Reflux; A.4.3 Synthesis of benzothiazole-7-carboxylic acid methyl ester; Isoamyl nitrite (22.0 mmol) is added to a solution of 2-amino-benzothiazole-7-carboxylic acid methyl ester (10.1 mmol) in THF (29 mL). The mixture is heated to reflux for 4h, the solvents are removed in vacuo and the residue is purified by flash chromatography (gradient: heptane to EtOAc/heptane 4/6) to give the desired product. LC-MS: tR = 0.85 min; [M+H]+ = 194.0.
  • 2
  • [ 1038509-28-2 ]
  • [ 677304-83-5 ]
YieldReaction ConditionsOperation in experiment
At 00C an aqueous NaOH solution (50%, 6.0 rnL) is added to a solution of benzothiazole- 7-carboxylic acid methyl ester in a mixture of MeOH (39 mL), THF (11.7 mL) and water (3.0 mL). The mixture is stirred for 4h and concentrated in vacuo. At 00C water (60 mL) is added and the mixture is made acidic (pH 5) by addition of cone, hydrochloric acid. After 30 min the precipitate is filtered off, washed with water and dried in vacuo to give the desired product. LC-MS : tR = 0.77 min; [M+CH3CN+H]+ = 221.1.
A.4.4 Synthesis of benzothiazole-7-carboxylic acid; At 00C an aq. NaOH solution (50%, 6.0 mL) is added to a solution of benzothiazole-7- carboxylic acid methyl ester in a mixture of MeOH (39 mL), THF (11.7 mL) and water (3.0 mL). The mixture is stirred for 4h and concentrated in vacuo. At 00C water (60 mL) is added and the mixture is made acidic (pH 5) by addition of cone, hydrochloric acid. After <n="61"/>30 min the precipitate is filtered off, washed with water and dried in vacuo to give the desired product. LC-MS: tR = 0.77 min; [M+CH3CN+H]+ = 221.1.
  • 3
  • [ 4518-10-9 ]
  • [ 1038509-28-2 ]
  • 4
  • [ 192948-00-8 ]
  • [ 1038509-28-2 ]
  • 5
  • [ 1038509-28-2 ]
  • [ 79-31-2 ]
  • methyl 2-isopropylbenzo[d]thiazole-7-carboxylate [ No CAS ]
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