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3-(ISOTHIOCYANATOMETHYL)HEPTANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21663-56-9

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21663-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21663-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,6 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21663-56:
(7*2)+(6*1)+(5*6)+(4*6)+(3*3)+(2*5)+(1*6)=99
99 % 10 = 9
So 21663-56-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NS/c1-3-5-6-9(4-2)7-10-8-11/h9H,3-7H2,1-2H3/t9-/m1/s1

21663-56-9SDS

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 3-(isothiocyanatomethyl)heptane

1.2 Other means of identification

Product number -
Other names 2-ethylhexyl isothiocyanate

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:21663-56-9 SDS

21663-56-9Downstream Products

21663-56-9Relevant academic research and scientific papers

Synthesis and spectroscopic analysis of substituted 2-aminothiazolines

Ferreira, Renan B.,Tormena, Claudio F.,Almeida, Wanda P.

, p. 186 - 190 (2013/05/22)

2-Aminothiazolines can exist in two tautomeric species, amino and imino forms, which can theoretically exist as two stereoisomers. Several methods and techniques have been used to evaluate tautomeric process, but in this case 15N NMR spectrosco

A general and facile one-pot process of isothiocyanates from amines under aqueous conditions

Sun, Nan,Li, Bin,Shao, Jianping,Mo, Weimin,Hu, Baoxiang,Shen, Zhenlu,Hu, Xinquan

experimental part, p. 61 - 70 (2012/04/04)

A general and facile one-pot protocol for the preparation of a broad range of alkyl and aryl isothiocyanates has been developed from their corresponding primary amines under aqueous conditions. This synthetic process involves an in situ generation of a dithiocarbamate salt from the amine substrate by reacting with CS2 followed by elimination to form the isothiocyanate product with cyanuric acid as the desulfurylation reagent. The choice of solvent is of decisive importance for the successful formation of the dithiocarbamate salt particularly for highly electron-deficient substrates. This novel and economical method is suitable for scale-up activities.

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