ETHYL 2-BROMO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE
- Product Name
- ETHYL 2-BROMO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE
- CAS No.
- 22900-83-0
- Chemical Name
- ETHYL 2-BROMO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE
- Synonyms
- ETHYL 2-BROMO-4-METHYLTHIAZOLE-5-CARBOXYLATE;2-bromo-4-methylthiazole-5-carboxylate;ETHYL 2-BROMO-4-METHYLTHIAZOLE-5-CARBOX&;Ethyl 2-bromo-4-methylthiazol-5-carboxylate;Ethyl 2-Bromo-4-methyl-5-thiazolecarboxylate;Ethyl 2-broMo-4-Methylthiazole-5-carboxylate 97%;Ethyl 2-Bromo-4-methylthiazole-5-carboxylate >Ethyl 2-bromop4-methyl-1,3-thiazole-5-carboxylate;ETHYL 2-BROMO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE;2-Bromo-4-methyl-5-thiazolecarboxylic acid ethyl ester
- CBNumber
- CB4205566
- Molecular Formula
- C7H8BrNO2S
- Formula Weight
- 250.11
- MOL File
- 22900-83-0.mol
ETHYL 2-BROMO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE Property
- Melting point:
- 65-69 °C(lit.)
- Boiling point:
- 287.1±20.0 °C(Predicted)
- Density
- 1.573±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- form
- powder to crystal
- pka
- -0.10±0.10(Predicted)
- color
- Light yellow to Brown
- Water Solubility
- Insoluble in water.
- InChI
- InChI=1S/C7H8BrNO2S/c1-3-11-6(10)5-4(2)9-7(8)12-5/h3H2,1-2H3
- InChIKey
- CFBIOWPDDZPIDP-UHFFFAOYSA-N
- SMILES
- S1C(C(OCC)=O)=C(C)N=C1Br
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H315Causes skin irritation
H317May cause an allergic skin reaction
H318Causes serious eye damage
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
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
- 645990
- Product name
- Ethyl 2-bromo-4-methylthiazole-5-carboxylate
- Purity
- 97%
- Packaging
- 1g
- Price
- $54.1
- Updated
- 2023/01/07
- Product number
- 645990
- Product name
- Ethyl 2-bromo-4-methylthiazole-5-carboxylate
- Purity
- 97%
- Packaging
- 5g
- Price
- $207
- Updated
- 2023/01/07
- Product number
- E0945
- Product name
- Ethyl 2-Bromo-4-methylthiazole-5-carboxylate
- Purity
- >97.0%(GC)
- Packaging
- 1g
- Price
- $41
- Updated
- 2025/07/31
- Product number
- E0945
- Product name
- Ethyl 2-Bromo-4-methylthiazole-5-carboxylate
- Purity
- >97.0%(GC)
- Packaging
- 5g
- Price
- $132
- Updated
- 2024/03/01
- Product number
- E900558
- Product name
- Ethyl 2-Bromo-4-methylthiazole-5-carboxylate
- Packaging
- 50mg
- Price
- $60
- Updated
- 2021/12/16
ETHYL 2-BROMO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE Chemical Properties,Usage,Production
Chemical Properties
White powder
Uses
It finds its application in the preparation of thiazole-4- and -5-carboxylates, and an infrared study of their rotational isomers and in the discovery of thiazolylpyridinone SCD1 inhibitors with preferential liver distribution and reduced mechanism-based adverse effects.
Synthesis
7210-76-6
22900-83-0
General procedure for the synthesis of ethyl 2-bromo-4-methyl-1,3-thiazole-5-carboxylate from ethyl 2-amino-4-methylthiazole-5-carboxylate: first, 2-methyl-1-nitro-propyl-propene (28.2 mL, 2.1 eq.) was dissolved in acetonitrile (700 mL) and the solution was cooled to 0 °C. Subsequently, bromo-trimethyl-silane (32 mL , 2.1 eq.). The reaction mixture was maintained at 0°C. Next, ethyl 2-amino-4-methyl-thiazole-5-carboxylate (18.6 g, 0.1 mol) was added to an acetonitrile/ethyl acetate (75/25) solution. After the dropwise addition was completed, the reaction mixture continued to be kept at 0°C. The mixture was warmed to room temperature and stirred for 24 hours. After completion of the reaction, the solvent was removed by evaporation and water was added. The product was extracted with ethyl acetate, the organic phase was dried with anhydrous sodium sulfate, filtered and concentrated. Finally, purification by fast chromatography using dichloromethane as eluent gave ethyl 2-bromo-4-methyl-1,3-thiazole-5-carboxylate as a yellow solid (21.74 g, 87 mmol, 87% yield); GC/MS analysis: [M+] C7H8BrNO2S 250.
References
[1] Patent: WO2004/6923, 2004, A1. Location in patent: Page/Page column 38
[2] Patent: WO2004/6924, 2004, A1. Location in patent: Page/Page column 31-32
[3] Patent: WO2004/7493, 2004, A1. Location in patent: Page 24-25
[4] Patent: EP2518054, 2012, A1. Location in patent: Page/Page column 53
[5] Patent: WO2008/47109, 2008, A1. Location in patent: Page/Page column 38
ETHYL 2-BROMO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from ETHYL 2-BROMO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE manufacturers
- Product
- ETHYL 2-BROMO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE 22900-83-0
- Price
- US $1.00/kg
- Min. Order
- 1kg
- Purity
- 98%
- Supply Ability
- 200kg
- Release date
- 2018-12-20