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100850-70-2

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100850-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100850-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,5 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100850-70:
(8*1)+(7*0)+(6*0)+(5*8)+(4*5)+(3*0)+(2*7)+(1*0)=82
82 % 10 = 2
So 100850-70-2 is a valid CAS Registry Number.

100850-70-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methyl-3-oxobutyl) thiocyanate

1.2 Other means of identification

Product number -
Other names Thiocyanic acid,2-methyl-3-oxobutyl ester (9CI)

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:100850-70-2 SDS

100850-70-2Downstream Products

100850-70-2Relevant articles and documents

FORMATION OF ISOMERIC β-ISOTHIOCYANATO AND β-THIOCYANATO CARBONYL COMPOUNDS IN THE REACTION OF THIOCYANIC ACID WITH α,β-UNSATURATED ALDEHYDES AND KETONES

Peretokin, A. V.,Shutalev, A. D.,Chupin, V. V.,Mergenova, A. M.,Ignatova, L. A.,et al.

, p. 912 - 918 (2007/10/02)

The structure of the products from the reaction of α,β-unsaturated aldehydes and ketones with thiocyanic acid was established by IR and 1H and 13C NMR spectroscopy.It was shown that the addition temperature and the structure of the obtained product depend on the structures of the initial compounds.It was established that the reactions of α,β-unsaturated aldehydes and ketones not containing methyl substituents at the Cβ carbon atom lead to the formation of isomeric β-isothiocyanato and β-thiocyanato carbonyl compounds, whereas the β-isothionato derivatives are formed exclusively in the case of t he β-methyl- and β,β-dimethyl substituted α,β-unsaturated aldehydes and ketones.

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