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19781-68-1

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19781-68-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19781-68-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,8 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19781-68:
(7*1)+(6*9)+(5*7)+(4*8)+(3*1)+(2*6)+(1*8)=151
151 % 10 = 1
So 19781-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H12/c1-3-6-4-5(6)2/h5-6H,3-4H2,1-2H3

19781-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name CIS-1-ETHYL-2-METHYLCYCLOPROPANE

1.2 Other means of identification

Product number -
Other names cis-1-ethyl-2-methyl-cyclopropane

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:19781-68-1 SDS

19781-68-1Downstream Products

19781-68-1Relevant articles and documents

Reactivity and Intersystem Crossing of Singlet Methylene in Solution

Turro, Nicholas J.,Cha, Yuan,Gould, Ian R.

, p. 2101 - 2107 (2007/10/02)

Evidence is reported wich demonstrates that singlet methylene, produced from the photolysis of diazomethane or diazirine undergoes intersystem crossing to form triplet methylene in perfluorohexane solvent.The results of triplet sensitized photolysis and of direct photolysis experiments with dilute concentrations of substrate (cis- and trans-2-pentene and chloroform) appear to be essentially identical.Stern-Volmer analyses of the competition kinetics between acetonitrile and 2-pentenes or chloroform for singlet methylene are consistent with the near diffusion controlled reactivity of singlet methylene.With the assumption of diffusion-controlled reactions for singlet methylene, plots of the quantum yield for singlet vs. triplet reaction for methylene allow the first estimate (-1) of the rate of intersystem crossing of singlet methylene in the condensed phase.This value is considerably smaller than the value that is extrapolated to the solution phase from results in the gas phase.The possible reasons for this difference are discussed.

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