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Acetic acid, butoxy[[(phenylmethoxy)carbonyl]amino]-, butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58237-85-7

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58237-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58237-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,3 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58237-85:
(7*5)+(6*8)+(5*2)+(4*3)+(3*7)+(2*8)+(1*5)=147
147 % 10 = 7
So 58237-85-7 is a valid CAS Registry Number.

58237-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name butyl 2-butoxy-2-(phenylmethoxycarbonylamino)acetate

1.2 Other means of identification

Product number -
Other names N-benzyloxycarbonyl-2-n-butoxyglycine n-butyl ester

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:58237-85-7 SDS

58237-85-7Relevant academic research and scientific papers

Preparation of protected α-alkoxyglycines

Kawai, Masao,Hosoda, Kouji,Omori, Yoshimasa,Yamada, Keiichi,Hayakawa, Shoko,Yamamura, Hatsuo,Butsugan, Yasuo

, p. 1545 - 1554 (2007/10/03)

N-Carbobenzoxy-α-alkoxyglycine esters were synthesized by H2SO4-catalyzed O-alkylation of N-carbobenzoxy-α-hydroxyglycine and also by base treatment of N-carbobenzoxy-N-chloroglycine methyl ester in the corresponding alcohol. Saponification of the protected α-alkoxyglycines gave free acids which can be used for the synthesis of α-alkoxyglycine residue-containing peptides.

Process for preparing substituted glycines

-

, (2008/06/13)

A new process is disclosed for the preparation of N-acyl-α-aromatic and N-acyl-α-heteroaromatic glycines by reaction of an α-ester or ether of an N-acylglycine ester or acid with an aromatic or heteroaromatic compound. Also disclosed are new intermediates for preparing N-acyl-α-aromatic and N-acyl-α-heteroaromatic glycines.

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