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Phenol, 2,6-bis(1,1-dimethylethyl)-4-(1-methyl-1H-indol-3-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88973-01-7

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88973-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88973-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,7 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88973-01:
(7*8)+(6*8)+(5*9)+(4*7)+(3*3)+(2*0)+(1*1)=187
187 % 10 = 7
So 88973-01-7 is a valid CAS Registry Number.

88973-01-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-ditert-butyl-4-(1-methylindol-3-yl)phenol

1.2 Other means of identification

Product number -
Other names Phenol,2,6-bis(1,1-dimethylethyl)-4-(1-methyl-1H-indol-3-yl)

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:88973-01-7 SDS

88973-01-7Downstream Products

88973-01-7Relevant academic research and scientific papers

RhII-Catalyzed Intermolecular C?H Arylation of Aromatics with Diazo Quinones

Wu, Kai,Cao, Bei,Zhou, Cong-Ying,Che, Chi-Ming

supporting information, p. 4815 - 4819 (2018/03/21)

We developed an efficient synthesis of biaryls by a dirhodium(II)-catalyzed aromatic C?H arylation with diazo quinones. The new biaryl synthesis can be performed under mild and neutral conditions and without directing group chelation assistance. The reaction tolerates various functionalities and is applicable to a broad range of aromatics. The regioselectivity of the C?H arylation was often high and predictable. The synthetic utility of the method was demonstrated by the late-stage modifications of a series of pharmaceuticals and functional materials as well as a short synthesis of a transthyretin amyloid inhibitor.

Studies on the synthesis and anti-inflammatory activity of 2,6-Di-tert-butylphenols with a heterocyclic group at the 4-position I

Isomura, Yasuo,Ito, Noriki,Homma, Hiroshige,Abe, Tetsushi,Kubo, Kazuo

, p. 3168 - 3178 (2007/10/02)

A number of 2,6-di-tert-butylphenols with a heterocyclic group at the 4-position were prepared. The heterocyclic groups were as follows: benzoxazole, benzothiazole, benzimidazole, indole, imidazo[1,2-a]pyridine and imidazo[1,2-a]pyrimidine. Anti-inflammat

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