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4-CHLORO-2-METHYLPHENYL ISOCYANIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60515-59-5

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60515-59-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60515-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,1 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60515-59:
(7*6)+(6*0)+(5*5)+(4*1)+(3*5)+(2*5)+(1*9)=105
105 % 10 = 5
So 60515-59-5 is a valid CAS Registry Number.

60515-59-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-1-isocyano-2-methylbenzene

1.2 Other means of identification

Product number -
Other names 4-Chlor-2-methyl-phenylisocyanid

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:60515-59-5 SDS

60515-59-5Relevant academic research and scientific papers

Synthesis of Isoselenocyanates

Zakrzewski, Jerzy,Huras, Bogumi?a,Kie?czewska, Anna

, p. 85 - 96 (2015/12/26)

Isoselenocyanates were synthesized by two methods under phase-transfer conditions (50% aq NaOH, CH2Cl2, Aliquat 336); the first started from isocyanides and selenium and gave isoselenocyanates in 61-89% yields, while the second started from amines and used chloroform and selenium, by applying sequentially the Hofmann isonitrile synthesis and the addition of selenium, in 4-70% yields.

Electrochemical generation of alkyl and aryl isocyanides

Guirado, Antonio,Zapata, Andres,Gomez, Jesus L.,Trabalon, Luis,Galvez, Jesus

, p. 9631 - 9640 (2007/10/03)

An efficient and widely applicable reagent-free method for the synthesis of alkyl and aryl isocyanides has been established. The electrochemical reduction of alkyl and aryl carbonimidoyl dichlorides under constant cathode potential leads to the corresponding isocyanides in almost quantitative yields. The availability of the starting materials, the mildness of the reaction conditions as well as the easy isolation of products are noteworthy, advantageous features of the procedure.

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