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944283-06-1

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944283-06-1 Usage

General Description

BOC-SER(FMOC-GLY)-OH is a chemical compound composed of three amino acid residues: BOC-SER, FMOC-GLY, and OH. BOC-SER is a form of serine with a tert-butyloxycarbonyl (BOC) protecting group, FMOC-GLY is a form of glycine with a 9-fluorenylmethyloxycarbonyl (FMOC) protecting group, and OH represents the carboxylic acid group. These amino acids are often used in peptide synthesis and can be deprotected to create free amine and carboxylic acid groups for further chemical reactions. BOC-SER(FMOC-GLY)-OH is commonly used in the laboratory for the production of peptides and other biological molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 944283-06-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,2,8 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 944283-06:
(8*9)+(7*4)+(6*4)+(5*2)+(4*8)+(3*3)+(2*0)+(1*6)=181
181 % 10 = 1
So 944283-06-1 is a valid CAS Registry Number.

944283-06-1SDS

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 L-Serine, N-[(1,1-dimethylethoxy)carbonyl]-O-[N-[(9H-fluoren-9-ylmethoxy)carbonyl]glycyl]-

1.2 Other means of identification

Product number -
Other names BOC-SER(GLY-FMOC)-OH

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:944283-06-1 SDS

944283-06-1Downstream Products

944283-06-1Relevant articles and documents

"o-Acyl isopeptide method" for peptide synthesis: Synthesis of forty kinds of "o-acyl isodipeptide unit" Boc-Ser/Thr(Fmoc-Xaa)-OH

Yoshiya, Taku,Taniguchi, Atsuhiko,Sohma, Youhei,Fukao, Fukue,Nakamura, Setsuko,Abe, Naoko,Ito, Nui,Skwarczynski, Mariusz,Kimura, Tooru,Hayashi, Yoshio,Kiso, Yoshiaki

, p. 1720 - 1730 (2007)

The O-acyl isopeptide method has recently received attention as an efficient synthetic method for peptides. Herein, forty kinds of "O-acyl isodipeptide unit" Boc-Ser/Thr(Fmoc-Xaa)-OH (1-40) were effectively synthesized in two-steps without epimerization. The O-acyl isodipeptide units are important building blocks to enable the routine use of the O-acyl isopeptide method. This journal is The Royal Society of Chemistry.

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