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60509-43-5

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60509-43-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60509-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,0 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60509-43:
(7*6)+(6*0)+(5*5)+(4*0)+(3*9)+(2*4)+(1*3)=105
105 % 10 = 5
So 60509-43-5 is a valid CAS Registry Number.

60509-43-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Butyl-(3-methyl-benzyl)-amine

1.2 Other means of identification

Product number -
Other names N-(3-Methylbenzyl)butan-1-amine

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:60509-43-5 SDS

60509-43-5Downstream Products

60509-43-5Relevant articles and documents

EFFECTS OF SUBSTITUENTS IN THE BENZYL BROMIDE ON THE KINETICS OF THE BENZYLATION OF AMINES

Shpan'ko, I. V.,Korostylev, A. P.,Rusu, L. N.

, p. 1715 - 1723 (2007/10/02)

The kinetics of the reactions of 3- and 4-substituted benzyl bromides with amines having various structures in nitrobenzene at 40 deg C were investigated.The 4-substituted benzyl bromides have higher reactivity compared with that calculated on the basis of the linear correlations according to the Hammett-Taft equation for unsubstituted and 3-substituted benzyl bromides containing electron-withdrawning substituents.The reactivity of benzyl bromides containing electron-donating substituents obeys a linear correlation with the ?+ constants.The effects of structural changes in the substrate and the nucleophile on the character of the transition states of the investigated reactions is discussed.

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