2-Methylthiazole-4-carboxamide
- Product Name
- 2-Methylthiazole-4-carboxamide
- CAS No.
- 31825-95-3
- Chemical Name
- 2-Methylthiazole-4-carboxamide
- Synonyms
- 2-Methyl-4-thiazolecarboxamide;4-THIAZOLECARBOXAMIDE, 2-METHYL-;2-Methyl-1,3-oxazole-4-carboamide
- CBNumber
- CB3776092
- Molecular Formula
- C5H6N2OS
- Formula Weight
- 142.18
- MOL File
- 31825-95-3.mol
2-Methylthiazole-4-carboxamide Property
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
Safety
- Hazard Note
- Harmful
- HS Code
- 2934100090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- M331740
- Product name
- 2-Methylthiazole-4-carboxamide
- Packaging
- 100mg
- Price
- $60
- Updated
- 2021/12/16
- Product number
- P000724685
- Product name
- 2-Methylthiazole-4-carboxamide
- Purity
- 97%
- Packaging
- 100mg
- Price
- $54
- Updated
- 2021/12/16
- Product number
- P000724685
- Product name
- 2-Methylthiazole-4-carboxamide
- Purity
- 97%
- Packaging
- 250mg
- Price
- $81
- Updated
- 2021/12/16
- Product number
- OR29665
- Product name
- 2-Methyl-1,3-thiazole-4-carboxamide
- Packaging
- 250mg
- Price
- $86
- Updated
- 2021/12/16
- Product number
- 8H48-1-X2
- Product name
- 2-Methyl-1,3-thiazole-4-carboxamide
- Packaging
- 250mg
- Price
- $95
- Updated
- 2021/12/16
2-Methylthiazole-4-carboxamide Chemical Properties,Usage,Production
Uses
2-Methylthiazole-4-carboxamide is a useful reactant for the synthesis of bisthiazole-?based histone deacetylase inhibitors.
Synthesis
6436-59-5
31825-95-3
Step 1. Synthesis of 2-methylthiazole-4-carboxamide (Compound 2A) Ethyl 2-methylthiazole-4-carboxylate (Compound 1, 0.8 g, 4.68 mmol) was mixed with an ethanol solution of ammonia (NH3/EtOH, 10 mL) and the reaction was stirred at 60 °C for 6 days. After completion of the reaction, the mixture was concentrated under reduced pressure to give the crude product. The crude product was purified by column chromatography (eluent: petroleum ether/ethyl acetate=1:1) to afford 2-methylthiazole-4-carboxamide (Compound 2, 0.44 g, 77% yield) as a white solid.
References
[1] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 8, p. 1203 - 1208
[2] Patent: WO2011/106414, 2011, A1. Location in patent: Page/Page column 83
[3] Journal of the Chemical Society, 1946, p. 91
[4] Journal of Organic Chemistry, 2009, vol. 74, # 15, p. 5750 - 5753
[5] Journal of the American Chemical Society, 2011, vol. 133, # 15, p. 5900 - 5904
2-Methylthiazole-4-carboxamide Preparation Products And Raw materials
Raw materials
Preparation Products
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