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610800-48-1

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610800-48-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 610800-48-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,0,8,0 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 610800-48:
(8*6)+(7*1)+(6*0)+(5*8)+(4*0)+(3*0)+(2*4)+(1*8)=111
111 % 10 = 1
So 610800-48-1 is a valid CAS Registry Number.

610800-48-1SDS

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 N-methyl-N-4-nitrophenylsulfonyl-L-alanine methyl ester

1.2 Other means of identification

Product number -
Other names N-methyl-N-nosyl-L-alanine methyl 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:610800-48-1 SDS

610800-48-1Downstream Products

610800-48-1Relevant articles and documents

MACROCYCLIC COMPOUNDS FOR THE TREATMENT OF MEDICAL DISORDERS

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Page/Page column 453; 545; 546, (2020/03/29)

Compounds, methods of use, and processes for making inhibitors of complement factor D or a pharmaceutically acceptable salt or composition thereof are provided. The inhibitors described herein target factor D and inhibit or regulate the complement cascade. The inhibitors of factor D described herein reduce excessive activation of complement.

"One-pot" methylation of N-nosyl-α-amino acid methyl esters with diazomethane and their coupling to prepare N-methyl dipeptides

Di Gioia, Maria Luisa,Leggio, Antonella,Le Pera, Adolfo,Liguori, Angelo,Napoli, Anna,Siciliano, Carlo,Sindona, Giovanni

, p. 7416 - 7421 (2007/10/03)

N-Nosyl-α-amino acid methyl esters are methylated quantitatively with diazomethane. After proper deprotection of the amino function by treatment with the reagent system mercaptoacetic acid/sodium methoxide, the obtained N-methyl amino acid methyl esters are coupled with N-Fmoe amino acid chlorides to afford the corresponding dipeptides. The obtained products do not show any detectable extent of racemization by 1H NMR and HPLC.

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