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2778-34-9

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2778-34-9 Usage

General Description

Glycine, N-[N-[(phenylmethoxy)carbonyl]-L-phenylalanyl]-, ethyl ester is a chemical compound commonly referred to as glycine ethyl ester. It is a derivative of the amino acid glycine and is often used in the synthesis of peptides and proteins. Glycine, N-[N-[(phenylmethoxy)carbonyl]-L-phenylalanyl]-, ethyl ester has potential applications in the pharmaceutical industry, particularly in the development of drug delivery systems and as a building block for various chemical reactions. Glycine ethyl ester is also used in research and laboratory settings as a reagent and intermediate in organic synthesis. It is important to handle this compound with care and follow proper safety precautions due to its potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 2778-34-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,7 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2778-34:
(6*2)+(5*7)+(4*7)+(3*8)+(2*3)+(1*4)=109
109 % 10 = 9
So 2778-34-9 is a valid CAS Registry Number.

2778-34-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Cbz-Phe-Gly-OEt

1.2 Other means of identification

Product number -
Other names Cbz-Phe-Gly-O-Et

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2778-34-9 SDS

2778-34-9Relevant articles and documents

Solar and Visible Light Assisted Peptide Coupling

Mishra, Abhaya K.,Parvari, Galit,Santra, Sourav K.,Bazylevich, Andrii,Dorfman, Ortal,Rahamim, Jonatan,Eichen, Yoav,Szpilman, Alex M.

supporting information, p. 12406 - 12412 (2021/04/05)

Amino acid and peptide couplings are widely used in fields related to pharma and materials. Still, current peptide synthesis continues to rely on the use of expensive, water sensitive, and waste-generating coupling reagents, which are often prepared in mu

Phosphine-based redox catalysis in the direct traceless staudinger ligation of carboxylic acids and azides

Kosal, Andrew D.,Wilson, Erin E.,Ashfeld, Brandon L.

supporting information, p. 12036 - 12040 (2013/01/16)

Redox catalysis: Aryl amides, imides, lactams, and dipeptides are obtained through a direct Staudinger ligation mediated by phosphine-based redox catalysis (see scheme). Mechanistic studies indicate the involvement of a phosphonium carboxylate intermediate that leads to a 1,3-acyl migration and thus results in C-N bond formation. Copyright

Design, synthesis, and application of enantioselective coupling reagent with a traceless chiral auxiliary

Kolesinska, Beata,Kaminski, Zbigniew J.

supporting information; experimental part, p. 765 - 768 (2009/09/06)

(Chemical Equation Presented) Stable chiral N-triazinylbrucinium tetrafluoroborate enantioselectively activates racemic carboxylic acids yielding enantiomerically enriched amides, esters, and dipeptides with er from 8:92 to 0.5:99.5. Due to the departure

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