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"Benzyl {2-[(2-hydroxyethyl)amino]-2-oxoethyl}carbamate" is a complex organic compound with the molecular formula C12H16N2O4. It is a carbamate derivative, which means it contains a carbamic acid group (-COO-NH2) bonded to a benzyl group. The compound features a 2-oxoethyl chain with an amino group attached to the 2-hydroxyethyl moiety, indicating the presence of an amide linkage. This chemical structure suggests potential applications in pharmaceuticals or as a chemical intermediate due to its reactivity and the presence of functional groups that can form hydrogen bonds. The compound's specific properties and uses would depend on its stability, solubility, and reactivity, which are not detailed in this summary.

4815-67-2

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4815-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4815-67-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4815-67:
(6*4)+(5*8)+(4*1)+(3*5)+(2*6)+(1*7)=102
102 % 10 = 2
So 4815-67-2 is a valid CAS Registry Number.

4815-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyloxycarbonylglycylaminoethanol

1.2 Other means of identification

Product number -
Other names -

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:4815-67-2 SDS

4815-67-2Relevant academic research and scientific papers

Enol esters as intermediates for the facile conversion of amino acids into amides and dipeptides

Kabouche,Bruneau,Dixneuf

, p. 5359 - 5362 (2007/10/02)

N-Protected amino enol esters are easily transformed at room temperature into amino amides, and in the presence of potassium cyanide as catalyst, into tertiary amides and dipeptides.

Amino alcohols as C-Terminal Protecting Groups in Peptide Synthesis

Kashima, Choji,Harada, Kazuo,Fujioka, Yoko,Maruyama, Tatsuya,Omote, Yoshimori

, p. 535 - 540 (2007/10/02)

The synthesis of peptides using amino alcohols as C-terminal protecting groups is described.C-Terminal protection of amino acid could be accomplished by reduction of the terminal carboxyl group to a hydroxymethyl group, and regeneration of the carboxyl group could be achieved by Jones' oxidation.This method was applied to the formation of di- and tripeptides.

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