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1-(4-hydroxy-5-isopropyl-2-methyl-phenyl)-propan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37847-36-2

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37847-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37847-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,8,4 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 37847-36:
(7*3)+(6*7)+(5*8)+(4*4)+(3*7)+(2*3)+(1*6)=152
152 % 10 = 2
So 37847-36-2 is a valid CAS Registry Number.

37847-36-2SDS

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 1-(4-hydroxy-5-isopropyl-2-methyl-phenyl)-propan-1-one

1.2 Other means of identification

Product number -
Other names 1-(4-Hydroxy-5-isopropyl-2-methyl-phenyl)-propan-1-on

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:37847-36-2 SDS

37847-36-2Downstream Products

37847-36-2Relevant academic research and scientific papers

Lewis Acids Catalysed Fries Rearrangement of Isopropylcresol Esters

Martin, Robert,Demerseman, Pierre

, p. 227 - 236 (2007/10/02)

In the course of the Fries rearrangement, aluminium chloride frequently induces migration or elimination of alkyl groups.The results obtained with titanium tetrachloride for the synthesis of vicinal o-hydroxyketones are compared with those obtained with aluminium chloride for some aliphatic and aromatic esters of isopropylcresols.In order to understand the migration and elimination processes occurring, the stabilities of the o-hydroxyketones are studied in the presence of aluminium chloride at different temperatures.Furthermore, all-vicinal o-hydroxyketones were prepared by the Fries rearrangement of 6-tert-butyl-p-thymol with titanium tetrachloride.

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