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198543-64-5

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198543-64-5 Usage

General Description

FMOC-D-ALPHA-T-BUTYLGLYCINE is a chemical compound that falls under the category of amino acids and derivatives. It is a derivative of the natural amino acid glycine, with added protection and modification groups. The compound is commonly used in peptide synthesis as a building block for creating peptide chains. Its structure contains a fluorenylmethyloxycarbonyl (FMOC) protecting group, which is commonly used in solid phase peptide synthesis. FMOC-D-ALPHA-T-BUTYLGLYCINE is utilized in both research and industrial settings for the production of peptides with specific sequences and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 198543-64-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,5,4 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 198543-64:
(8*1)+(7*9)+(6*8)+(5*5)+(4*4)+(3*3)+(2*6)+(1*4)=185
185 % 10 = 5
So 198543-64-5 is a valid CAS Registry Number.

198543-64-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3,3-dimethylbutanoic acid

1.2 Other means of identification

Product number -
Other names Fmoc-tert-leucine

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:198543-64-5 SDS

198543-64-5Upstream product

198543-64-5Relevant articles and documents

Sterically biased 3,3-sigmatropic rearrangement of azides: Efficient preparation of nonracemic α-amino acids and heterocycles

Gagnon, David,Lauzon, Sophie,Godbout, Cedrickx,Spino, Claude

, p. 4769 - 4771 (2007/10/03)

(Chemical Equation Presented) Homochiral α-amino acids, heterocycles, and carbocycles are efficiently constructed via a short sequence of reactions starting from the chiral auxiliary p-menthane-3-carboxaldehyde. The key feature of the sequence is a highly selective tandem Mitsunobu/3,3-sigmatropic rearrangement of hydrazoic acid that procures enantiomerically enriched allylic azides. The sequence is either terminated by oxidative cleavage to provide amino acids or by ring-closing metathesis to provide heterocycles or carbocycles bearing nitrogen.

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