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2-(2-(Methylsulfonyloxy)ethyl)-4-nitrobenzyl (Methanesulfonate), commonly known as Mitsunobu reagent, is a versatile chemical compound with the molecular formula C11H13NO7S2. It is a white to light yellow solid and has a molecular weight of 331.36 g/mol. This reagent is widely used in organic synthesis as a protecting group for alcohols, amines, and thiols, making it a valuable tool in the synthesis of pharmaceutical and agrochemical compounds.

199014-22-7

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199014-22-7 Usage

Uses

Used in Organic Synthesis:
2-(2-(Methylsulfonyloxy)ethyl)-4-nitrobenzyl (Methanesulfonate) is used as a protecting group in organic synthesis for [application reason] to facilitate the selective reactions of functional groups in complex molecules.
Used in Peptide Synthesis:
In the pharmaceutical industry, 2-(2-(Methylsulfonyloxy)ethyl)-4-nitrobenzyl (Methanesulfonate) is used as a reagent in peptide synthesis for [application reason] to protect the functional groups of amino acids, allowing for the stepwise assembly of peptide chains.
Used as a Precursor in Pharmaceutical and Agrochemical Compounds:
2-(2-(Methylsulfonyloxy)ethyl)-4-nitrobenzyl (Methanesulfonate) is used as a precursor in the synthesis of various pharmaceutical and agrochemical compounds for [application reason] to provide a versatile intermediate for the development of new drugs and agrochemicals.
Used in Research and Industrial Settings:
Due to its versatility in organic synthesis, 2-(2-(Methylsulfonyloxy)ethyl)-4-nitrobenzyl (Methanesulfonate) is widely used in both research and industrial settings for [application reason] to enable the development of novel chemical entities and improve the efficiency of existing synthetic routes.

Check Digit Verification of cas no

The CAS Registry Mumber 199014-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,0,1 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 199014-22:
(8*1)+(7*9)+(6*9)+(5*0)+(4*1)+(3*4)+(2*2)+(1*2)=147
147 % 10 = 7
So 199014-22-7 is a valid CAS Registry Number.

199014-22-7SDS

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 2-{2-[(Methylsulfonyl)oxy]ethyl}-4-nitrobenzyl methanesulfonate

1.2 Other means of identification

Product number -
Other names Benzoic acid,2-[[[(4-methoxyphenyl)amino]acetyl]amino]

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:199014-22-7 SDS

199014-22-7Relevant academic research and scientific papers

BICYCLOANILINE DERIVATIVE

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Page/Page column 65, (2010/04/25)

The invention relates to a compound of a general formula (I): wherein A1 and A2 each mean a nitrogen atom or an optionally-substituted methine group; Ring B means a 5-membered to 7-membered aliphatic ring, or a spiro or bicyclo ring formed from the aliphatic ring and any other 3-membered to 7-membered aliphatic ring; R1 means a hydrogen atom, or an optionally-substituted C1-C6 alkyl group, or an optionally-substituted aryl, aralkyl or heteroaryl group; R2 means an optionally-substituted aryl, aralkyl or heteroaryl group; and X means a group of =NH or =O, etc. Based on its excellent Wee1 kinase-inhibitory effect, the compound of the invention has cell growth-inhibitory effect and has an additive/synergistic effect with any other anticancer agent, and is therefore useful in the field of medicine.

Oxazolidinones having a benzannulated 6- or 7-membered heterocycle

-

, (2008/06/13)

The present invention provides oxazolidinones having a benzannelated 6- or 7-membered heterocycle as antibacterial agents.

An efficient synthesis of 6-substituted 2-(2H-[1,2,4]triazol-3- ylmethyl)-1,2,3,4-tetrahydro-isoquinolines

Urban, Frank J.,Breitenbach, Ralph

, p. 645 - 653 (2007/10/03)

A synthesis of 6-nitro and 6-amino 2-(2H-[1,2,4]triazol-3- ylmethyl)1,2,3,4-tetrahydro-isoquinolines using a bis-alkylation process is described. 5-(Aminomethyl)-1-(p-methoxybenzyl)-triazole was prepared by a regioselective route from 1,2,4-triazole.

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