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106916-72-7

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106916-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106916-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,9,1 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106916-72:
(8*1)+(7*0)+(6*6)+(5*9)+(4*1)+(3*6)+(2*7)+(1*2)=127
127 % 10 = 7
So 106916-72-7 is a valid CAS Registry Number.

106916-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name l-menthyl chloroacetate

1.2 Other means of identification

Product number -
Other names (-)-menthylchloroacetate

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:106916-72-7 SDS

106916-72-7Relevant articles and documents

Novel ketoprofen–antioxidants mutual codrugs as safer nonsteroidal anti-inflammatory drugs: Synthesis, kinetic and pharmacological evaluation

Sehajpal, Shikha,Prasad, Deo Nandan,Singh, Rajesh K.

, (2019)

Ketoprofen belongs to one of the most common nonsteroidal anti-inflammatory drugs (NSAIDs) but its clinical usefulness has been restricted due to the high incidence of gastrointestinal complications. The release of reactive oxygen species (ROS) in NSAIDs

Solvent- and base-free dicyclohexylcarbodiimide-promoted esterifications

Streinz,Koutek,?aman

, p. 809 - 811 (2001)

N,N'-Dicyclohexylcarbodiimide/base-promoted esterification of carboxylic acids containing α-halogen atom(s) gave low yields of products when performed in a solvent. This failure was found to be due to the low stability of appropriate intermediates under t

Synthesis, characterization and applications of some novel DMAP-based chiral ionic liquids

Singh, Avtar,Chopra, Harish Kumar

, p. 106 - 111 (2018)

A convenient and efficient procedure for the synthesis of some novel chiral ionic liquids (CILs) from 4-dimethylaminopyridinium cation has been reported. The synthesis of the CILs includes the treatment of optically active (?)-menthyl ester with 4-dimethy

SYNTHESIS AND STRUCTURE OF AMINO ESTERS OF MENTHOL

Raikova, T. S.,Kalechits, G. V.,Manukov, E. N.,Vyalimyae, T. K.,Makhach, S. A.

, p. 526 - 529 (1981)

The conditions for the acylation of (-)-menthol with monochloroacetyl chloride have been studied.Amino esters of (-)-menthol have been obtained by the nuclephilic replacement of the chlorine in (-)-menthol monochloroacetate by residues of secondary amines

-

Sisido,K. et al.

, p. 4878 - 4881 (1961)

-

Stereoselective oxidation of methyl phenyl sulfide in the presence of chiral ionic liquids

Akopyan,Rakhmanov,Grigor'Ev,Ryzhov,Tarakanova,Anisimov

, p. 1302 - 1307 (2014)

Several ionic liquids containing a chiral center either in the cation or in the anion have been prepared. They have been applied as catalysts and solvents for stereoselective oxidation of methyl phenyl sulfide to obtain the respective sulfoxide.

Catalytic Sc(OTf)3 mediated direct asymmetric aldol reaction of (?)-menthyl isothiocyanatoacetate with aldehydes by using (?)-menthol as chiral auxiliary

Bhangare, Dattatraya N.,Shinde, Rohit G.,Pawar, Pushpalata D.,Nikalje, Milind D.,Lokhande, Mahendra N.

supporting information, p. 1878 - 1882 (2021/05/27)

This method involves the direct asymmetric aldol reaction of (?)-menthyl isothiocyanatoacetate 5 with a variety of substituted aromatic aldehydes, which offers a convenient method for the synthesis of intermediate containing biologically relevant α-amino

Preparation method of Gboxin

-

Paragraph 0022; 0031-0033; 0043-0045; 0054-0056, (2020/08/27)

The invention relates to a preparation method of Gboxin. The method comprises the following steps: reacting o-phenylenediamine with n-propanal; preparing 2-ethyl-1H-benzimidazole, carrying out N-alkylation reaction on 2-ethyl-1H-benzimidazole and chloroacetic acid-L-menthyl ester to generate 2-(2-ethyl-1H-benzimidazole) L-menthyl acetate, carrying out methylation by using iodomethane to generate abenzimidazolium salt, and finally, exchanging iodine ions into chloride ions by using chlorine ion exchange resin to obtain the final product Gboxin. The method has the advantages of short process route, mild conditions, simple operation and low equipment requirements, and the obtained product has the advantages of high purity and high yield, and is suitable for industrial production.

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