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107454-75-1

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107454-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107454-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,4,5 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 107454-75:
(8*1)+(7*0)+(6*7)+(5*4)+(4*5)+(3*4)+(2*7)+(1*5)=121
121 % 10 = 1
So 107454-75-1 is a valid CAS Registry Number.

107454-75-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-adamantyl(4-bicyclo[2.2.1]heptanyl)diazene

1.2 Other means of identification

Product number -
Other names cis-N-1-Adamantyl-N'-1-norbornyldiazene

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:107454-75-1 SDS

107454-75-1Downstream Products

107454-75-1Relevant articles and documents

cis-Diazenes. Viscosity Effects, One-Bond Scission, and Cis-Trans Isomerization

Neuman, Robert C.,Grow, Richard H.,Binegar, Glen A.,Gunderson, Howard J.

, p. 2682 - 2688 (2007/10/02)

Effects of solvent viscosity on the rates of overall thermal decomposition, deazatization, and iomerization of several symmetric and unsymmetric cis-diazenes (cis-azoalkanes) have been determined in pure alkanes and mixtures of octane and mineral oil.Increasing viscosity decreases the overall decomposition and deazatization rates for all of these cis-diazenes.While isomerization rates also decrease with increasing viscosity for most of the diazenes, that for cis-N-tert-butyl-N'-1-norbornyldiazene (1) increases.These results are interpreted in terms of deazatization via one-bond scission and an intermediate diazenyl radical, isomerization via nonradical inversion, and the possibility of isomerization via a diazenyl radical for 1.

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