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Benzene, [3-[(methylsulfinyl)methoxy]-1-propenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138899-41-9

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138899-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138899-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,8,9 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 138899-41:
(8*1)+(7*3)+(6*8)+(5*8)+(4*9)+(3*9)+(2*4)+(1*1)=189
189 % 10 = 9
So 138899-41-9 is a valid CAS Registry Number.

138899-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-((methylsulfinyl)methoxy)prop-1-en-1-yl)benzene

1.2 Other means of identification

Product number -
Other names -

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:138899-41-9 SDS

138899-41-9Downstream Products

138899-41-9Relevant academic research and scientific papers

Formyl cyanide: A stable species. Experimental and theoretical studies

Lewis-Bevan, Wyn,Gaston, Rick D.,Tyrrell, James,Stork, Wilmer D.,Salmon, Gary L.

, p. 1933 - 1935 (2007/10/02)

Formyl cyanide has been generated by the retro-ene cleavage of cinnamyloxyacetonitrile using flash vacuum pyrolysis. Isolation of pure formyl cyanide in the gas phase has shown that the compound is much more stable than originally reported, with a measured half-life of 45.5 h under our experimental conditions. Formyl cyanide readily reacts with water to form hydrogen cyanide and formic acid. The observed vibrational frequencies are compared with the results of high-level ab initio calculations. Ab initio calculations are also reported for the transition state and the intrinsic reaction pathway of formyl cyanide into the products HCN and CO. The calculations are in agreement with the experimental observation that formyl cyanide does not undergo a unimolecular decomposition to HCN and CO as originally suggested.

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