7-(bromomethyl)quinoline hydrobromide

Base Information

Chemical Name:7-(bromomethyl)quinoline hydrobromide
CAS No.:188874-61-5
Molecular Formula:BrH*C₁₀H₈BrN
Molecular Weight:302.996
Hs Code.:
Mol file:188874-61-5.mol

Synonyms:Quinoline,7-(bromomethyl)-, hydrobromide (9CI); 7-(Bromomethyl)quinoline hydrobromide

Suppliers and Price of 7-(bromomethyl)quinoline hydrobromide

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

Labseeker
7-(bromomethyl)quinolinehydrobromide 95
1g
$ 1050.00

Frontier Specialty Chemicals
7-Bromomethylquinolinehydrobromide 95%
1g
$ 581.00

Frontier Specialty Chemicals
7-Bromomethylquinolinehydrobromide 95%
500mg
$ 361.00

Crysdot
7-(Bromomethyl)quinolinehydrobromide 97%
1g
$ 696.00

Chemenu
7-(Bromomethyl)quinolinehydrobromide 97%
1g
$ 657.00

Total 5 raw suppliers

Chemical Property of 7-(bromomethyl)quinoline hydrobromide

Chemical Property:

PSA：12.89000
LogP:4.08780

Purity/Quality:

99% ^*data from raw suppliers

7-(bromomethyl)quinolinehydrobromide 95 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 7-(bromomethyl)quinoline hydrobromide

There total 4 articles about 7-(bromomethyl)quinoline hydrobromide 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: 98.0%

: 39982-49-5
(quinolin-7-yl)methanol

: 188874-61-5
7-bromomethyl-quinoline hydrobromide

Guidance literature:: With hydrogen bromide; acetic acid; at 70 ℃;
DOI:10.1016/S0960-894X(99)00196-1

Reference yield:

: 346-55-4
4-chloro-7-trifluoromethyl quinoline

: 188874-61-5
7-bromomethyl-quinoline hydrobromide

Guidance literature:: Multi-step reaction with 4 steps

1: 82 percent / H₂ / 5 percent Pd/C / methanol / Ambient temperature

2: 1.) 30 percent oleum / 1.) 150 deg C, 2.) reflux

3: 85 percent / sodium dihydiro-bis-(2-methoxyethoxy)aluminate / tetrahydrofuran / -20 °C

4: 98 percent / HBr, AcOH / 70 °C

With sulfuric acid; hydrogen bromide; hydrogen; acetic acid; sodium bis(2-methoxyethoxy)aluminium dihydride; palladium on activated charcoal; In tetrahydrofuran; methanol;
DOI:10.1016/S0960-894X(99)00196-1

Reference yield:

: 51552-68-2
quinoline-7-carboxylic acid methyl ester

: 188874-61-5
7-bromomethyl-quinoline hydrobromide

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / sodium dihydiro-bis-(2-methoxyethoxy)aluminate / tetrahydrofuran / -20 °C

2: 98 percent / HBr, AcOH / 70 °C

With hydrogen bromide; acetic acid; sodium bis(2-methoxyethoxy)aluminium dihydride; In tetrahydrofuran;
DOI:10.1016/S0960-894X(99)00196-1