Benzyl 2-(1H-benzo[d][1,2,3]triazol-1-yl)-2-oxoethylcarbamate

Base Information Edit

Chemical Name:Benzyl 2-(1H-benzo[d][1,2,3]triazol-1-yl)-2-oxoethylcarbamate
CAS No.:173459-80-8
Molecular Formula:C₁₆H₁₄N₄O₃
Molecular Weight:310.312
Hs Code.:
Mol file:173459-80-8.mol

Synonyms:benzyl [2?(1H?benzo[d][1,2,3]triazol?1?yl)?2?oxoethyl]carbamate

Suppliers and Price of Benzyl 2-(1H-benzo[d][1,2,3]triazol-1-yl)-2-oxoethylcarbamate

Supply Marketing:Edit

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

Sigma-Aldrich
Z-Gly-Bt 97%
50mg
$ 74.70

Total 2 raw suppliers

Chemical Property of Benzyl 2-(1H-benzo[d][1,2,3]triazol-1-yl)-2-oxoethylcarbamate Edit

Chemical Property:

Melting Point:110-117°C
Storage Temp.:?20°C

Purity/Quality:

99% ^*data from raw suppliers

Z-Gly-Bt 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Benzotriazole amino acids, or aminoacylbenzotriazolides, are versatile reagents for synthesizing peptides as well as their mimetics and conjugates. Benzotriazole amino acids have been used for the preparation of diverse derivatives including:Polypeptidal benzotriazolidesPeptidomimetics, such as aminoxypeptides, depsipeptides and heterocyclic peptidomimeticsTagged peptides and peptidomimetics, particularly those with fluorescent labelsN, O, S, and C linked peptide conjugates

Technology Process of Benzyl 2-(1H-benzo[d][1,2,3]triazol-1-yl)-2-oxoethylcarbamate

There total 1 articles about Benzyl 2-(1H-benzo[d][1,2,3]triazol-1-yl)-2-oxoethylcarbamate 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: 93.0%

: 95-14-7,27556-51-0
1,2,3-Benzotriazole

: 1138-80-3
N-(Benzyloxycarbonyl)glycine

: 173459-80-8
benzyl [2?(1H?benzo[d][1,2,3]triazol?1?yl)?2?oxoethyl]carbamate

Guidance literature:: 1,2,3-Benzotriazole; With thionyl chloride; In dichloromethane; at 25 ℃; for 0.5h;

N-(Benzyloxycarbonyl)glycine; In dichloromethane; at 25 ℃; for 3h;
DOI:10.1007/s00706-020-02579-5