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24006-09-5

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24006-09-5 Usage

General Description

1-Mesitylhydrazine hydrochloride is a chemical compound with the molecular formula C9H14N2Cl. It is a derivative of hydrazine, and it has a mesityl group attached to the nitrogen atom. 1-Mesitylhydrazine hydrochloride is primarily used in organic synthesis for the preparation of various pharmaceuticals, pesticides, and other fine chemicals. It also exhibits potential biological activity, making it a useful tool for research in the fields of pharmacology and biotechnology. Additionally, 1-Mesitylhydrazine hydrochloride is a hydrazine derivative, and as such, it should be handled with caution due to its toxic and potentially hazardous properties.

Check Digit Verification of cas no

The CAS Registry Mumber 24006-09-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,0 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24006-09:
(7*2)+(6*4)+(5*0)+(4*0)+(3*6)+(2*0)+(1*9)=65
65 % 10 = 5
So 24006-09-5 is a valid CAS Registry Number.

24006-09-5SDS

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 Mesitylhydrazine hydrochloride (1:1)

1.2 Other means of identification

Product number -
Other names 2,4,6-TRIMETHYLPHENYLHYDRAZINE HYDROCHL&Mesitylhydrazine hydrochloride

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:24006-09-5 SDS

24006-09-5Upstream product

24006-09-5Relevant articles and documents

1,4-Bis-Dipp/Mes-1,2,4-Triazolylidenes: Carbene Catalysts That Efficiently Overcome Steric Hindrance in the Redox Esterification of α- And β-Substituted α,β-Enals

Yatham, Veera Reddy,Harnying, Wacharee,Kootz, Darius,Neud?rfl, J?rg-M.,Schl?rer, Nils E.,Berkessel, Albrecht

supporting information, p. 2670 - 2677 (2016/03/12)

As reported by Scheidt and Bode in 2005, sterically nonencumbered α,β-enals are readily converted to saturated esters in the presence of alcohols and N-heterocyclic carbene catalysts, e.g., benzimidazolylidenes or triazolylidenes. However, substituents at the α- or β-position of the α,β-enal substrate are typically not tolerated, thus severely limiting the substrate spectrum. On the basis of our earlier mechanistic studies, a set of N-Mes- or N-Dipp-substituted 1,2,4-triazolium salts were synthesized and evaluated as (pre)catalysts in the redox esterification of various α- or β-substituted enals. In particular the 1,4-bis-Mes/Dipp-1,2,4-triazolylidenes overcome the above limitations and efficiently catalyze the redox esterification of a whole series of α/β-substituted enals hitherto not amenable to NHC-catalyzed transformations. The synthetic value of 1,4-bis-Mes/Dipp-1,2,4-triazolylidenes is further demonstrated by the one-step bicyclization of 10-oxocitral to (racemic) nepetalactone in diastereomerically pure form.

α-Aroyloxyaldehydes: Scope and limitations as alternatives to α-haloaldehydes for NHC-catalysed redox transformations

Ling, Kenneth B.,Smith, Andrew D.

supporting information; experimental part, p. 373 - 375 (2011/02/24)

α-Aroyloxyaldehydes are readily prepared bench stable synthetic intermediates. Their ability to act as α-haloaldehyde surrogates for NHC-promoted redox esterifications and in [4+2] cycloadditions is described.

ENANTIOSELECTVE REACTIONS CATALYZED BY CHIRAL TRIAZOLIUM SALTS

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Page/Page column 54-55, (2010/11/28)

This invention provides a convenient method for converting imines and other electrophiles into heterocyclic ring systems. The process does not require the use of metallic reagents, and is catalyzed by an organic heterocyclic carbene catalyst. Accordingly,

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