2,6-diMethyliMidazo[1,2-a]pyriMidine-3-carboxylic acid

Base Information

Chemical Name:2,6-diMethyliMidazo[1,2-a]pyriMidine-3-carboxylic acid
CAS No.:1335052-44-2
Molecular Formula:C9H9N3O2
Molecular Weight:191.189
Hs Code.:2933399990
Mol file:1335052-44-2.mol

Synonyms:2,6-diMethyliMidazo[1,2-a]pyriMidine-3-carboxylic acid

Suppliers and Price of 2,6-diMethyliMidazo[1,2-a]pyriMidine-3-carboxylic acid

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

Matrix Scientific
2,6-Dimethylimidazo[1,2-a]pyrimidine-3-carboxylic acid
1g
$ 5586.00

Crysdot
2,6-Dimethylimidazo[1,2-a]pyrimidine-3-carboxylicacid 95+%
1g
$ 3795.00

Alichem
2,6-Dimethylimidazo[1,2-a]pyrimidine-3-carboxylicacid
1g
$ 3217.20

Total 7 raw suppliers

Chemical Property of 2,6-diMethyliMidazo[1,2-a]pyriMidine-3-carboxylic acid

Chemical Property:

PSA：67.49000
LogP:1.04430

Purity/Quality:

97% ^*data from raw suppliers

2,6-Dimethylimidazo[1,2-a]pyrimidine-3-carboxylic acid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2,6-diMethyliMidazo[1,2-a]pyriMidine-3-carboxylic acid

There total 2 articles about 2,6-diMethyliMidazo[1,2-a]pyriMidine-3-carboxylic acid 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: 49.0%

: 1335054-73-3
ethyl 2,6-dimethylimidazo[1,2-a]pyrimidine-3-carboxylate

: 1335052-44-2
2,6-dimethylimidazo[1,2-a]pyrimidine-3-carboxylic acid

Guidance literature:: ethyl 2,6-dimethylimidazo[1,2-a]pyrimidine-3-carboxylate; With lithium hydroxide; In ethanol; at 20 ℃; for 36h; Inert atmosphere;

With hydrogenchloride; In water; pH=3; Inert atmosphere; Cooling with ice;
DOI:10.1016/j.bmcl.2014.05.062

Reference yield:

: 50840-23-8
5-methylpyrimidin-2-amine

: 1335052-44-2
2,6-dimethylimidazo[1,2-a]pyrimidine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydrogencarbonate / 1,2-dimethoxyethane / 36 h / Inert atmosphere; Reflux

2.1: lithium hydroxide / ethanol / 36 h / 20 °C / Inert atmosphere

2.2: pH 3 / Inert atmosphere; Cooling with ice

With sodium hydrogencarbonate; lithium hydroxide; In 1,2-dimethoxyethane; ethanol;
DOI:10.1016/j.bmcl.2014.05.062

Reference yield: 49.0%

: 5071-96-5
3-METHOXYBENZYLAMINE

: 1335052-44-2
2,6-dimethylimidazo[1,2-a]pyrimidine-3-carboxylic acid

: 1300031-43-9
N-(3-methoxybenzyl)-2,6-dimethylimidazo[1,2-a]pyrimidine-3-carboxamide

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In acetonitrile; at 20 ℃; for 12h; Inert atmosphere;
DOI:10.1021/ml200036r