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Phenol, 2-(1-methyl-1-propenyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62191-66-6

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62191-66-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62191-66-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,9 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62191-66:
(7*6)+(6*2)+(5*1)+(4*9)+(3*1)+(2*6)+(1*6)=116
116 % 10 = 6
So 62191-66-6 is a valid CAS Registry Number.

62191-66-6SDS

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 (E)-o-(but-2-en-2-yl)phenol

1.2 Other means of identification

Product number -
Other names 2-((E)-1-Methyl-propenyl)-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:62191-66-6 SDS

62191-66-6Downstream Products

62191-66-6Relevant academic research and scientific papers

Photochemical Reactions of o-Alkenylphenols and 1-Alkenyl-2-naphthol with Alkylamines: Amination via Photoinduced Proton Transfer

Yasuda, Masahide,Sone, Tatsuya,Tanabe, Kimiko,Shima, Kensuke

, p. 459 - 464 (2007/10/02)

Irradiation of o-alkenylphenols 1a-c and 2a-e in the presence of alkylamines gave o-(1-alkylaminoalkyl)phenols 4a-n and 5a-e in relatively good yields.Deprotonation of these o-alkenylphenols by the amines occurs in the excited singlet state to give the excited singlet state of the phenolate anion 7 and the ammonium ion.The proton transfer from the ammonium ion to the alkenyl group of 7 generates the zwitterion 8 that allows the nucleophilic addition of the amine at the benzylic cation centre.Similar photoamination of 1-(2-methylpropenyl)-2-naphthol 3 with alkylamines occured to give 1-(1-alkylamino-2-methylpropyl)-2-naphthols 6a-b.

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