Basic information Safety Supplier Related

4-METHYL-2-(3-PYRIDINYL)-1,3-THIAZOLE-5-CARBOXYLIC ACID

Basic information Safety Supplier Related

4-METHYL-2-(3-PYRIDINYL)-1,3-THIAZOLE-5-CARBOXYLIC ACID Basic information

Product Name:
4-METHYL-2-(3-PYRIDINYL)-1,3-THIAZOLE-5-CARBOXYLIC ACID
Synonyms:
  • 2-(3-PYRIDYL)-4-METHYLTHIAZOLE-5-CARBOX&
  • 4-METHYL-2-PYRID-3-YLTHIAZOLE-5-CARBOXYLIC ACID
  • 4-Methyl-2-(pyridin-3-yl)-1,3-thiazole-5-carboxylic acid 95%
  • 5-Thiazolecarboxylic acid, 4-Methyl-2-(3-pyridinyl)-
  • 4-Methyl-2-(3-pyridinyl)-5-thiazolecarboxylic acid
  • TIMTEC-BB SBB011441
  • ASISCHEM C71524
  • ASINEX-REAG BAS 07676575
CAS:
39091-01-5
MF:
C10H8N2O2S
MW:
220.25
Product Categories:
  • Thiazole
  • Carboxylic Acids
  • Thiazoles, Isothiazoles & Benzothiazoles
  • Building Blocks
  • Heterocyclic Building Blocks
  • Thiazoles
  • Carboxylic Acids
  • Thiazoles, Isothiazoles &Benzothiazoles
Mol File:
39091-01-5.mol
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4-METHYL-2-(3-PYRIDINYL)-1,3-THIAZOLE-5-CARBOXYLIC ACID Chemical Properties

Melting point:
244-248 °C (dec.)(lit.)
Boiling point:
459.0±55.0 °C(Predicted)
Density 
1.381±0.06 g/cm3(Predicted)
solubility 
DMF: 1.5 mg/ml; DMSO: 2 mg/ml; DMSO:PBS(pH7.2) (1:1): 0.5 mg/ml
form 
A crystalline solid
pka
1.71±0.37(Predicted)
InChI
1S/C10H8N2O2S/c1-6-8(10(13)14)15-9(12-6)7-3-2-4-11-5-7/h2-5H,1H3,(H,13,14)
InChIKey
CJLQNROYBZEUGH-UHFFFAOYSA-N
SMILES
Cc1nc(sc1C(O)=O)-c2cccnc2
CAS DataBase Reference
39091-01-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2934100090
Storage Class
13 - Non Combustible Solids
Hazard Classifications
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3

MSDS

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4-METHYL-2-(3-PYRIDINYL)-1,3-THIAZOLE-5-CARBOXYLIC ACID Usage And Synthesis

Description

2-(3-pyridyl)-4-methyl-Thiazole-5-carboxylic acid is a synthetic intermediate useful for pharmaceutical synthesis.

Uses

2-(3-Pyridyl)-4-methyl-thiazole-5-carboxylic acid is a synthetic intermediate useful for pharmaceutical synthesis.

Synthesis

1. Synthesis of ethyl 2-bromo-4-methylthiazole-5-carboxylate: Ethyl 2-amino-4-methylthiazole-5-carboxylate is diazotized and brominated (with CuBr?).
2. Synthesis of target product: The bromo compound from step 1 undergoes Suzuki coupling with pyridine-3-boronic acid pinacol ester in the presence of Pd catalysts (XPhos-Pd-G2, XPhos).

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