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2-tert-butyl-6-ethylphenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63551-41-7

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63551-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63551-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,5 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63551-41:
(7*6)+(6*3)+(5*5)+(4*5)+(3*1)+(2*4)+(1*1)=117
117 % 10 = 7
So 63551-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O/c1-5-9-7-6-8-10(11(9)13)12(2,3)4/h6-8,13H,5H2,1-4H3

63551-41-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-tert-butyl-6-ethylphenol

1.2 Other means of identification

Product number -
Other names 2-Aethyl-6-tert-butyl-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:63551-41-7 SDS

63551-41-7Relevant academic research and scientific papers

Ruthenium-catalyzed rearrangement of cis-1-ethynyl-2-vinyloxiranes to substituted phenols

Maddirala, Shambabu Joseph,Odedra, Arjan,Taduri, Bhanu Pratap,Liu, Rai-Shung

, p. 1173 - 1176 (2007/10/03)

Catalytic cyclization of cis-1-ethynyl-2-vinyloxiranes was implemented with TpRuPPh3(CH3CN)2PF6 catalyst (10 mol%), to give 2,6-disubstituted phenols in reasonable yields. Under similar conditions, 1,1,2,2-tetrasubstituted oxirane gave the 2,3,6-trisubstituted phenol with skeleton reorganization. On the basis of 2H- and l3C-labeling results, we propose that the reaction mechanism involves electrocyclization of ruthenium-vinylidene intermediate with cleavage of the carbon-oxygen bond of the epoxide. Georg Thieme Verlag Stuttgart.

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