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69626-79-5

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69626-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69626-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,2 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69626-79:
(7*6)+(6*9)+(5*6)+(4*2)+(3*6)+(2*7)+(1*9)=175
175 % 10 = 5
So 69626-79-5 is a valid CAS Registry Number.

69626-79-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethylpropyl thiocyanate

1.2 Other means of identification

Product number -
Other names 2,2-dimethyl-1-thiocyanatopropane

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:69626-79-5 SDS

69626-79-5Downstream Products

69626-79-5Relevant articles and documents

Mechanism of the Triphenylphosphine-Tetrachloromethane-Alcohol Reaction: Pericyclic or Clustered Ion Pairs?

Slagle, J. D.,Huang, T. T.-S.,Franzus, B.

, p. 3526 - 3530 (1981)

The intermediate formed from tetrachloromethane-triphenylphosphine and neopentyl alcohol decomposes bimolecularly in acetonitrile and not unimolecularly as in CDCl3.This kinetic order is not consistent with a pericyclic pathway but is consistent with an ion-pair mechanism.Consistent with the ion-pair mechanism in acetonitrile is the incorporation of external nucleophiles in the neopentyl skeleton by addition of added nucleophiles to the system.Consistent with the enhanced polarity of acetonitrile is the increased amount of carbon-oxygen cleavage resulting in extensive racemization of the reaction product from (R)-(+)-2-octanol.The preparation of neopentyl thiocyanate and neopentyl isothiocyanate from the corresponding alcohol illustrates the synthetic utility of this reaction in more polar solvents.

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