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1262886-64-5

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1262886-64-5 Usage

General Description

(S)-N-Fmoc-2-(7'-octenyl)glycine is a chemical compound used in the field of organic chemistry, specifically in the synthesis of peptides and proteins. It is a derivative of glycine, an amino acid, with a fluorine-methyl-oxycarbonyl (Fmoc) protective group on the nitrogen atom and a 7'-octenyl side chain. The Fmoc group is commonly used in solid-phase peptide synthesis to protect the amino group, while the side chain modification of 7'-octenyl allows for the selective introduction of the desired functionality. (S)-N-Fmoc-2-(7'-octenyl)glycine is crucial for the development of novel bioactive peptides and pharmaceuticals, as well as in the study and manipulation of protein structure and function.

Check Digit Verification of cas no

The CAS Registry Mumber 1262886-64-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,8,8 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1262886-64:
(9*1)+(8*2)+(7*6)+(6*2)+(5*8)+(4*8)+(3*6)+(2*6)+(1*4)=185
185 % 10 = 5
So 1262886-64-5 is a valid CAS Registry Number.

1262886-64-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)dec-9-enoic acid

1.2 Other means of identification

Product number -
Other names -

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:1262886-64-5 SDS

1262886-64-5Downstream Products

1262886-64-5Relevant articles and documents

Robust asymmetric synthesis of unnatural alkenyl amino acids for conformationally constrained α-helix peptides

Aillard, Boris,Robertson, Naomi S.,Baldwin, Adam R.,Robins, Siobhan,Jamieson, Andrew G.

supporting information, p. 8775 - 8782 (2014/12/11)

The efficient asymmetric synthesis of unnatural alkenyl amino acids required for peptide 'stapling' has been achieved using alkylation of a fluorine-modified NiII Schiff base complex as the key step.

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