Succinimidyl-5-(bromoacetamido)pentanoate

Base Information

Chemical Name:Succinimidyl-5-(bromoacetamido)pentanoate
CAS No.:109880-15-1
Molecular Formula:C₁₁H₁₅BrN₂O₅
Molecular Weight:335.154
Hs Code.:2925190090
DSSTox Substance ID:DTXSID10703858
Nikkaji Number:J2.573.531E
Wikidata:Q82636128
Mol file:109880-15-1.mol

Synonyms:109880-15-1;Succinimidyl-5-(bromoacetamido)pentanoate;(2,5-dioxopyrrolidin-1-yl) 5-[(2-bromoacetyl)amino]pentanoate;DTXSID10703858;AKOS015909479;A2162;FT-0604058;5-(Bromoacetylamino)pentanoic acid succinimidyl ester;2,5-DIOXOPYRROLIDIN-1-YL 5-(2-BROMOACETAMIDO)PENTANOATE;2-Bromo-N-{5-[(2,5-dioxopyrrolidin-1-yl)oxy]-5-oxopentyl}acetamide;Pentanoic acid,5-[(2-bromoacetyl)amino]-,2,5-dioxo-1-pyrrolidinyl ester

Suppliers and Price of Succinimidyl-5-(bromoacetamido)pentanoate

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

Total 7 raw suppliers

Chemical Property of Succinimidyl-5-(bromoacetamido)pentanoate

Chemical Property:

PSA：96.27000
LogP:1.05320
XLogP3:0
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:334.01643
Heavy Atom Count:19
Complexity:369

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(=O)N(C1=O)OC(=O)CCCCNC(=O)CBr

Technology Process of Succinimidyl-5-(bromoacetamido)pentanoate

There total 2 articles about Succinimidyl-5-(bromoacetamido)pentanoate 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: 52.4%

: 6066-82-6
1-hydroxy-pyrrolidine-2,5-dione

: 109880-17-3
5-(2-Bromo-acetylamino)-pentanoic acid

: 109880-15-1
N-(δ-bromoacetamido-n-valeroyloxy)succinimide

Guidance literature:: With dicyclohexyl-carbodiimide; In acetonitrile; at 4 ℃;
DOI:10.1248/cpb.35.1991

Reference yield:

: 660-88-8
5-aminopentanoic acid

: 109880-15-1
N-(δ-bromoacetamido-n-valeroyloxy)succinimide

Guidance literature:: Multi-step reaction with 2 steps

1: 20 percent / pH 7.5-8.5

2: 52.4 percent / N,N'-dicyclohexylcarbodiimide / acetonitrile / 4 °C

With dicyclohexyl-carbodiimide; In acetonitrile;
DOI:10.1248/cpb.35.1991