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Phenol, 3-(pentylamino)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138452-75-2

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138452-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138452-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,5 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138452-75:
(8*1)+(7*3)+(6*8)+(5*4)+(4*5)+(3*2)+(2*7)+(1*5)=142
142 % 10 = 2
So 138452-75-2 is a valid CAS Registry Number.

138452-75-2SDS

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 3-(pentylamino)phenol

1.2 Other means of identification

Product number -
Other names 3-(N-n-pentylamino)phenol

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:138452-75-2 SDS

138452-75-2Downstream Products

138452-75-2Relevant academic research and scientific papers

Process for preparing 3-(N,N-disubstituted amino)phenol

-

, (2008/06/13)

A process for preparing a 3-(N,N-disubstituted amino)phenol is herein disclosed which comprises reacting resorcin with a primary amine represented by formula (2): wherein R1 is an alkyl group, a cycloalkyl group, an alkenyl group, an alkoxyalkyl group, an aryl group or an aralkyl group, terminating the reaction when the conversion of resorcin is 50 mol % or more and when the amount of an N,N'-disubstituted-m-phenylenediamine as a by-product is 2 mol % or less of the amount of used resorcin, adding an alkyl halide represented by formula (3): wherein R2 is an alkyl group or a cycloalkyl group; and X is a halogen atom, to the obtained reaction mixture, adding an aqueous alkaline solution to the resultant reaction mixture to dissolve unreacted resorcin in the aqueous phase, extracting the 3-(N,N-disubstituted amino)phenol with an organic solvent, and then recovering unreacted resorcin from the aqueous phase. According to this process, the high-purity 3-(N,N-disubstituted amino)phenol can be prepared from resorcin in a substantially high yield, the production of by-products being inhibited.

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