4-Thiazoleaceticacid,2-bromo-5-methyl-,methylester(9CI)

Base Information

Chemical Name:4-Thiazoleaceticacid,2-bromo-5-methyl-,methylester(9CI)
CAS No.:496062-15-8
Molecular Formula:C7H8BrNO2S
Molecular Weight:250.11
Hs Code.:2934999090
Mol file:496062-15-8.mol

Synonyms:4-Thiazoleaceticacid,2-bromo-5-methyl-,methylester(9CI)

Suppliers and Price of 4-Thiazoleaceticacid,2-bromo-5-methyl-,methylester(9CI)

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

SynQuest Laboratories
Methyl 2-(2-bromo-5-methyl-4-thiazolyl)acetate
1 g
$ 784.00

Crysdot
Methyl2-(2-Bromo-5-methyl-4-thiazolyl)acetate 95+%
1g
$ 329.00

American Custom Chemicals Corporation
METHYL-(2-BROMO-5-METHYL-1,3-THIAZOL-4-YL)ACETATE 95.00%
5MG
$ 500.71

Alichem
Methyl2-(2-Bromo-5-methyl-4-thiazolyl)acetate
25g
$ 3383.50

Alichem
Methyl2-(2-Bromo-5-methyl-4-thiazolyl)acetate
10g
$ 2090.40

Alichem
Methyl2-(2-Bromo-5-methyl-4-thiazolyl)acetate
5g
$ 1393.60

Total 6 raw suppliers

Chemical Property of 4-Thiazoleaceticacid,2-bromo-5-methyl-,methylester(9CI)

Chemical Property:

PSA：67.43000
LogP:1.92950

Purity/Quality:

97% ^*data from raw suppliers

Methyl 2-(2-bromo-5-methyl-4-thiazolyl)acetate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Methyl 2-(2-Bromo-5-methyl-4-thiazolyl)acetate is used in preparation of indane acetic acid and derivatives which are used in treatment or prevention of autoimmune and liver diseases.

Technology Process of 4-Thiazoleaceticacid,2-bromo-5-methyl-,methylester(9CI)

There total 5 articles about 4-Thiazoleaceticacid,2-bromo-5-methyl-,methylester(9CI) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 40.0%

: 259654-73-4
methyl (2-amino-5-methyl-1,3-thiazol-4-yl)acetate

: 496062-15-8
methyl (2-bromo-5-methyl-1,3-thiazol-4-yl)acetate

Guidance literature:: With tert.-butylnitrite; copper(ll) bromide; In acetonitrile; at -20 - 15 ℃; for 2h;

Reference yield: 40.0%

: 540-80-7
tert.-butylnitrite

: 105983-77-5
methyl 4-bromo-3-oxopentanoate

: 496062-15-8
methyl (2-bromo-5-methyl-1,3-thiazol-4-yl)acetate

Guidance literature:: With copper(ll) bromide; In acetonitrile; at -20 - 15 ℃; for 2h;

Reference yield:

: 30414-53-0
methyl propanoyl acetate

: 496062-15-8
methyl (2-bromo-5-methyl-1,3-thiazol-4-yl)acetate

Guidance literature:: Multi-step reaction with 3 steps

1: bromine / chloroform / 0 - 20 °C / Inert atmosphere

2: toluene / 1 h / 100 °C

3: copper(ll) bromide; tert.-butylnitrite / acetonitrile / 2 h / -20 - 15 °C

With tert.-butylnitrite; bromine; copper(ll) bromide; In chloroform; toluene; acetonitrile;