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118354-71-5

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  • 3-Pyrrolidinol,1-(phenylmethyl)-, 3-methanesulfonate, (3S)-

    Cas No: 118354-71-5

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118354-71-5 Usage

General Description

(S)-1-Benzyl-3-mesyloxy pyrrolidine is a chemical compound with a molecular formula C13H17NO2S. It is commonly used as a reagent in organic synthesis for the preparation of various pharmaceutical compounds. (S)-1-BENZYL-3-MESYLOXY PYRROLIDINE is characterized by a pyrrolidine ring structure with a benzyl group and a mesyloxy group attached to it. The mesyloxy group is a functional group that contains a sulfonyl group attached to an oxygen atom. The (S) configuration indicates that the compound has a specific stereoisomeric configuration, which can affect its properties and reactivity in chemical reactions. (S)-1-BENZYL-3-MESYLOXY PYRROLIDINE may have potential applications in the development of new drugs and other biologically active molecules due to its unique structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 118354-71-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,3,5 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 118354-71:
(8*1)+(7*1)+(6*8)+(5*3)+(4*5)+(3*4)+(2*7)+(1*1)=125
125 % 10 = 5
So 118354-71-5 is a valid CAS Registry Number.

118354-71-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-1-BENZYL-3-MESYLOXY PYRROLIDINE

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:118354-71-5 SDS

118354-71-5Relevant articles and documents

Development of a Dual-Acting Antibacterial Agent (TNP-2092) for the Treatment of Persistent Bacterial Infections

Ma, Zhenkun,Lynch, Anthony Simon

, p. 6645 - 6657 (2016/08/05)

The clinical management of prosthetic joint infections and other persistent bacterial infections represents a major unmet medical need. The rifamycins are one of the most potent antibiotic classes against persistent bacterial infections, but bacteria can

METHOD FOR PRODUCTION OF OPTICALLY ACTIVE 3-AMINO-NITROGENATED COMPOUND

-

Page/Page column 18, (2009/05/29)

Aiming at production of an optically active 3-amino nitrogen-containing compound which is useful as an intermediate in synthesis of medicines and pesticides, in particular, an optically active 1-protected-3-aminopyrrolidine derivative, from an inexpensive and readily available raw material by a process which is efficient and can be practiced industrially, an optically active 3-amino nitrogen-containing compound is produced by performing a reaction of an optically active 3-substituted nitrogen-containing compound with ammonia, methylamine, ethylamine or dimethylamine in the presence of water. In addition, a 1-protected-3-aminopyrrolidine derivative is produced by performing a reaction of an optically active 1-protected-3-(sulfonyloxy)pyrrolidine derivative with ammonia, methylamine, ethylamine, or dimethylamine in the presence of methanol, ethanol, n-propanol, or isopropanol under a pressure of less than 30 barr.

Synthesis of beta-proline like derivatives and their evaluation as sodium channel blockers

Muraglia, Marilena,Franchini, Carlo,Corbo, Filomena,Scilimati, Antonio,Sinicropi, Maria Stefania,De Luca, Annamaria,De Bellis, Michela,Camerino, Diana Conte,Tortorella, Vincenzo

, p. 1099 - 1103 (2008/09/17)

(Chemical Equation Presented) A simple and convenient procedure for the preparation of beta-proline like derivatives in their racemic and optically active forms has been reported. The compounds have been screened for their potential activity as sodium cha

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