(4-BroMo-benzylaMino)-acetic acid

Base Information

Chemical Name:(4-BroMo-benzylaMino)-acetic acid
CAS No.:1727-09-9
Molecular Formula:C9H10BrNO2
Molecular Weight:244.088
Hs Code.:2922499990
Mol file:1727-09-9.mol

Synonyms:2-(4-bromobenzylamino)acetic acid;(4-bromobenzylamino)acetic acid;N-(4-Brom-benzyl)-glycin;N-(4-bromobenzyl)glycine;

Suppliers and Price of (4-BroMo-benzylaMino)-acetic 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

Crysdot
(4-Bromo-benzylamino)-aceticacid 95+%
1g
$ 544.00

Chemenu
(4-Bromo-benzylamino)-aceticacid 96%
1g
$ 513.00

Activate Scientific
N-(4-Bromobenzyl)glycine 95%
5 g
$ 1197.00

Activate Scientific
N-(4-Bromobenzyl)glycine 95%
1 g
$ 379.00

Acrotein
N-(4-Bromobenzyl)glycine 97%
0.5g
$ 201.67

Total 10 raw suppliers

Chemical Property of (4-BroMo-benzylaMino)-acetic acid

Chemical Property:

PSA：49.33000
LogP:2.01420

Purity/Quality:

99.0% MIN ^*data from raw suppliers

(4-Bromo-benzylamino)-aceticacid 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (4-BroMo-benzylaMino)-acetic acid

There total 5 articles about (4-BroMo-benzylaMino)-acetic 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: 90.0%

: 1122-91-4
4-bromo-benzaldehyde

: 56-40-6,18875-39-3,25718-94-9
glycine

: 1727-09-9
2-(4-bromobenzylamino)acetic acid

Guidance literature:: With sodium tetrahydroborate; sodium hydroxide; In methanol; water; at 20 ℃; for 40h;
DOI:10.1016/j.bcp.2018.03.018

Reference yield: 71.0%

: 6000-43-7
2-aminoethanoic acid hydrochloride

: 1122-91-4
4-bromo-benzaldehyde

: 1727-09-9
2-(4-bromobenzylamino)acetic acid

Guidance literature:: 2-aminoethanoic acid hydrochloride; 4-bromo-benzaldehyde; With sodium hydroxide; In methanol; water; at 20 ℃; for 0.5h;

With sodium tetrahydroborate; In methanol; water; at 0 ℃; for 18h;
DOI:10.1021/jm200916p

Reference yield:

: 589-15-1
1-bromomethyl-4-bromobenzene

: 1727-09-9
2-(4-bromobenzylamino)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: (i) CHCl₃, (ii) aq. NH₃

2: aq. HBr

3: (i) benzene, (ii) aq. HBr

With hydrogen bromide;