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1018818-04-6

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  • Featured products (2R,4S)-1-tert-butoxycarbonyl-4-methylpyrrolidine-2-carboxylic acid

    Cas No: 1018818-04-6

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1018818-04-6 Usage

General Description

"(2R,4S)-1-Boc-4-Methylpyrrolidine-2-carboxylic acid" is a chemical compound with a molecular formula of C12H21NO4. It is a derivative of pyrrolidine and is commonly used as a building block in organic synthesis. The compound is a white solid at room temperature and is primarily used in the pharmaceutical industry for the production of various drugs and pharmaceutical intermediates. It is a chiral compound, meaning it has a non-superimposable mirror image, and its specific stereochemistry is important for its biological activity. The compound is also known by its systematic name N-[(2R,4S)-4-Methyl-2-pyrrolidinyl]-2-methylpropanamide and is often referred to by its abbreviation, (R,S)-Boc-4-Me-Proline.

Check Digit Verification of cas no

The CAS Registry Mumber 1018818-04-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,8,8,1 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1018818-04:
(9*1)+(8*0)+(7*1)+(6*8)+(5*8)+(4*1)+(3*8)+(2*0)+(1*4)=136
136 % 10 = 6
So 1018818-04-6 is a valid CAS Registry Number.

1018818-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,4S)-1-tert-butoxycarbonyl-4-methylpyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names (2R,4S)-4-Methyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl 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:1018818-04-6 SDS

1018818-04-6Relevant articles and documents

Total synthesis, NMR solution structure, and binding model of the potent histone deacetylase inhibitor FR235222

Rodriquez, Manuela,Terracciano, Stefania,Cini, Elena,Settembrini, Giulia,Bruno, Ines,Bifulco, Giuseppe,Taddei, Maurizio,Gomez-Paloma, Luigi

, p. 423 - 427 (2007/10/03)

An alternative route: The fungal metabolite FR235222, a potent inhibitor of mammalian histone deacetylase (HDAC), has been synthesized. Key steps are the preparation of unusual amino acids Ahoda and (2R,4S)-MePro. A 3D model for cyclopeptide inhibitor int

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