1H-Indazole-7-methanol, 5-bromo-

Base Information

Chemical Name:1H-Indazole-7-methanol, 5-bromo-
CAS No.:1360957-64-7
Molecular Formula:
Molecular Weight:227.06
Hs Code.:
Mol file:1360957-64-7.mol

Synonyms:

Suppliers and Price of 1H-Indazole-7-methanol, 5-bromo-

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

Chemcia Scientific
(1H-Indazol-7-yl)-methanol 95%
5 G
$ 965.00

Chemcia Scientific
(1H-Indazol-7-yl)-methanol 95%
1 G
$ 275.00

Total 2 raw suppliers

Chemical Property of 1H-Indazole-7-methanol, 5-bromo-

Chemical Property:

Purity/Quality:

98% ^*data from raw suppliers

(1H-Indazol-7-yl)-methanol 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1H-Indazole-7-methanol, 5-bromo-

There total 4 articles about 1H-Indazole-7-methanol, 5-bromo- 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: 76.1%

: 898747-24-5
methyl 5-bromo-1H-indazole-7-carboxylate

: 1360957-64-7
(5-bromo-1H-indazol-7-yl)methanol

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃; for 1h;

Reference yield:

: 4389-45-1
3-methylantranilic acid

: 1360957-64-7
(5-bromo-1H-indazol-7-yl)methanol

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetic acid; bromine / 4 h / 0 - 20 °C

2.1: caesium carbonate / N,N-dimethyl-formamide / 16 h / 0 - 20 °C

3.1: potassium acetate; acetic anhydride / chloroform / 1 h / 0 - 20 °C / Inert atmosphere

3.2: 4 h / 60 °C

4.1: lithium aluminium tetrahydride / tetrahydrofuran / 1 h / 0 - 20 °C

With lithium aluminium tetrahydride; bromine; potassium acetate; acetic anhydride; caesium carbonate; acetic acid; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;

Reference yield:

: 206548-13-2
2-amino-5-bromo-3-methylbenzoic acid

: 1360957-64-7
(5-bromo-1H-indazol-7-yl)methanol

Guidance literature:: Multi-step reaction with 3 steps

1.1: caesium carbonate / N,N-dimethyl-formamide / 16 h / 0 - 20 °C

2.1: potassium acetate; acetic anhydride / chloroform / 1 h / 0 - 20 °C / Inert atmosphere

2.2: 4 h / 60 °C

3.1: lithium aluminium tetrahydride / tetrahydrofuran / 1 h / 0 - 20 °C

With lithium aluminium tetrahydride; potassium acetate; acetic anhydride; caesium carbonate; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;