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8-Oxa-2,5-diaza-7-phosphadecanoic acid, 7-ethoxy-3,6-dimethyl-4-oxo-, phenylmethyl ester, 7-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54788-36-2

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54788-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54788-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,8 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54788-36:
(7*5)+(6*4)+(5*7)+(4*8)+(3*8)+(2*3)+(1*6)=162
162 % 10 = 2
So 54788-36-2 is a valid CAS Registry Number.

54788-36-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl N-(N-carbobenzyloxy-DL-alanyl)-1-aminoethylphosphonate

1.2 Other means of identification

Product number -
Other names [1-(2-Benzyloxycarbonylamino-propionylamino)-ethyl]-phosphonic acid diethyl 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:54788-36-2 SDS

54788-36-2Relevant academic research and scientific papers

STUDIES ON ORGANOPHOSPHORUS COMPOUNDS. 65, A FACILE SYNTHETIC ROUTE TO PHOSPHONOPEPTIDES

Yuan, Chengye,Wang, Guohong

, p. 207 - 212 (2007/10/02)

A direct procedure for the preparation of phosphonopeptides, containing either a N- or C-terminal phosphonic acid residue, is described.This method is based on a three component condensation reaction leading to diethyl 1-(N-carbobenzyloxyamino)-alkylphosp

STUDIES ON THE SYNTHESIS OF CHEMOTHERAPEUTICS. PART XI. SYNTHESIS AND ANTIBACTERIAL ACTIVITIES OF PHOSPHONOPEPTIDES

Kametani, Tetsuji,Kigasawa, Kazuo,Hiiragi, Mineharu,Wakisaka, Kikuo,Haga, Seiji,et al.

, p. 1205 - 1242 (2007/10/02)

A variety of phosphonopeptides, shown in 2 as a general formula, containg natural and/or unnatural amino acids were synthesized, and their in vitro antibacterial activities were examined.N-Protected amino acids were condensed with 1-amino-ethylphosphonic acid or its ester followed by deprotection and hydrolysis to give the requisite phosphonopeptides.Several compounds showed higher levels of activity against certain members of Gram-negative bacteria than those of Alafosfalin (1) as the standard phosphonopeptide.A brief discussion on structure-activity relationships is also described.

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