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Glycine, N-[[(4-nitrophenyl)methoxy]carbonyl]-, ethyl ester is a complex organic compound with the chemical formula C11H12N2O6. It is a derivative of glycine, an amino acid, and features a 4-nitrophenyl group attached to the carbonyl group, which is further esterified with an ethyl group. Glycine, N-[[(4-nitrophenyl)methoxy]carbonyl]-, ethyl ester is often used in peptide synthesis as a protecting group for the amino group, allowing for the controlled formation of peptide bonds. The 4-nitrophenyl group can be removed under mild acidic conditions, which is crucial for the deprotection step in peptide synthesis. Its molecular structure and reactivity make it a valuable tool in the field of biochemistry and pharmaceuticals for the assembly of complex peptide sequences.

4132-82-5

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4132-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4132-82-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,3 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4132-82:
(6*4)+(5*1)+(4*3)+(3*2)+(2*8)+(1*2)=65
65 % 10 = 5
So 4132-82-5 is a valid CAS Registry Number.

4132-82-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-nitrobenzyloxycarbonyl)glycine ethyl ester

1.2 Other means of identification

Product number -
Other names 4-Nitro-benzyloxycarbonyl-glycin-ethylester

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:4132-82-5 SDS

4132-82-5Relevant academic research and scientific papers

Synthetic and structural studies on 1,2,4-dithiazolidine-3,5-dione derivatives

Wood, Mark E.,Cane-Honeysett, Daniel J.,Dowle, Michael D.,Coles, Simon J.,Hursthouse, Michael B.

, p. 3015 - 3023 (2007/10/03)

Methods have been developed for the N-alkylation of 1,2,4-dithiazolidine-3,5-dione 2 and the subsequent conversion of the N-alkylated derivatives into isocyanates 5. An extension of this methodology onto a solid-support is also reported. X-ray crystallographic analysis has been carried out on potassium 1,2,4-dithiazolidine-3,5-dione 3 for structural comparison with the parent heterocycle 2.

1,2,4-Dithiazolidine-3,5-dione: A nucleophilic isocyanate 'building block'

Cane-Honeysett,Dowle,Wood

, p. 1622 - 1624 (2007/10/03)

Mild conditions are described for the direct N-alkylation of 1,2,4-dithiazolidine-3,5-dione 1 using a variety of alkyl halides with subsequent conversion of the products 2 into alkyl isocyanates using triphenylphosphine.

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