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60040-14-4

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60040-14-4 Usage

General Description

The chemical [1,1'-Biphenyl]-4-amine, 4'-pentyl- is a compound with the molecular formula C19H21N. It is a derivative of biphenyl with a pentyl group attached at the 4' position of the amine. The chemical is commonly used as a building block in the synthesis of various organic compounds and is also known for its potential biological activities, including antimicrobial and antiproliferative properties. It is important to handle this chemical with care and follow proper safety precautions when working with it in a laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 60040-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,4 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60040-14:
(7*6)+(6*0)+(5*0)+(4*4)+(3*0)+(2*1)+(1*4)=64
64 % 10 = 4
So 60040-14-4 is a valid CAS Registry Number.

60040-14-4SDS

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 4-(4-pentylphenyl)aniline

1.2 Other means of identification

Product number -
Other names 4-(p-pentylphenyl)aniline

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:60040-14-4 SDS

60040-14-4Relevant articles and documents

Novel and unexpected deamination during the palladium-catalysed cross- coupling of haloanilines and arylboronic acids

Hird, Michael,Seed, Alexander J.,Toyne, Kenneth J.

, p. 438 - 440 (2007/10/03)

Palladium-catalysed cross-coupling reactions involving haloanilines and arylboronic acids produce the expected biaryl products, but additionally a substantial quantity of the corresponding deaminated biaryl is also generated which constitutes a novel synthetic methodology.

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