AMINO-(2-BROMO-PHENYL)-ACETIC ACID METHYL ESTER HYDROCHLORIDE

Base Information

Chemical Name:AMINO-(2-BROMO-PHENYL)-ACETIC ACID METHYL ESTER HYDROCHLORIDE
CAS No.:1219408-44-2
Molecular Formula:C₉H₁₀BrNO₂*ClH
Molecular Weight:280.549
Hs Code.:

Synonyms:methyl (2-bromophenyl)glycinate hydrochloride

Suppliers and Price of AMINO-(2-BROMO-PHENYL)-ACETIC ACID METHYL ESTER HYDROCHLORIDE

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
Methyl amino(2-bromophenyl)acetate hydrochloride 95%+
1g
$ 524.00

Matrix Scientific
Methyl amino(2-bromophenyl)acetate hydrochloride 95%+
5g
$ 1728.00

Matrix Scientific
Methyl amino(2-bromophenyl)acetate hydrochloride 95%+
2.500g
$ 1144.00

Acrotein
Methyl2-amino-2-(2-bromophenyl)acetateHCl 97%
5g
$ 907.50

Total 2 raw suppliers

Chemical Property of AMINO-(2-BROMO-PHENYL)-ACETIC ACID METHYL ESTER HYDROCHLORIDE

Chemical Property:

Purity/Quality:

99% ^*data from raw suppliers

Methyl amino(2-bromophenyl)acetate hydrochloride 95%+ ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of AMINO-(2-BROMO-PHENYL)-ACETIC ACID METHYL ESTER HYDROCHLORIDE

There total 2 articles about AMINO-(2-BROMO-PHENYL)-ACETIC ACID METHYL ESTER HYDROCHLORIDE 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:

: 67-56-1
methanol

: 254762-66-8,339274-34-9
2-amino-2-(2-bromophenyl)acetic acid

: 1219408-44-2
methyl (2-bromophenyl)glycinate hydrochloride

Guidance literature:: With thionyl chloride; at 20 ℃; for 24h; Cooling with ice;
DOI:10.1016/j.tet.2011.04.064

Reference yield:

: 6630-33-7
ortho-bromobenzaldehyde

: 1219408-44-2
methyl (2-bromophenyl)glycinate hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1.1: ammonium chloride / methanol; water / 24.33 h / 20 °C

1.2: 72 h / Reflux

2.1: thionyl chloride / 24 h / 20 °C / Cooling with ice

With thionyl chloride; ammonium chloride; In methanol; water; 1.1: Strecker amino acid synthesis;
DOI:10.1016/j.tet.2011.04.064