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157360-23-1

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157360-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157360-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,3,6 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 157360-23:
(8*1)+(7*5)+(6*7)+(5*3)+(4*6)+(3*0)+(2*2)+(1*3)=131
131 % 10 = 1
So 157360-23-1 is a valid CAS Registry Number.

157360-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-ditert-butyl-2,2-dipentyl-3H-1-benzofuran-5-ol

1.2 Other means of identification

Product number -
Other names 4,6-ditert-butyl-2,2-dipentyl-3H-benzofuran-5-ol

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:157360-23-1 SDS

157360-23-1Downstream Products

157360-23-1Relevant articles and documents

A new strategy for the synthesis of 4,6-di-tert-butyl-2,2-dipentyl-2,3- dihydro-5-benzofuranol (BO-653), a potent antiatherogenic antioxidant

Murakata, Masatoshi,Kimura, Masahiro

scheme or table, p. 4950 - 4952 (2011/01/04)

An efficient alternative route to 4,6-di-tert-butyl-2,2-dipentyl-2,3- dihydro-5-benzofuranol (BO-653), a potent antiatherogenic antioxidant, has been developed by the application of the base-promoted dienone- phenol rearrangement reaction. A decisive effect of MgBr2 in the reaction of Grignard reagents is also described.

Process for preparation of a benzofuran derivative

-

Page/Page column 15, (2010/01/31)

An industrially useful process for producing benzofuran derivatives of formula (1) by formylating a compound of formula (2) (where A1 is a protective group), followed by reaction with a compound of formula (4) (where X1 is a halogen atom), then performing a cyclizing reaction and subsequently performing a reaction for hydroxyl group deprotection.

Prophylactic/therapeutic agents for atherosclerosis

-

, (2008/06/13)

PCT No. PCT/JP98/01861 Sec. 371 Date Nov. 8, 1999 Sec. 102(e) Date Nov. 8, 1999 PCT Filed Apr. 23, 1998 PCT Pub. No. WO98/50025 PCT Pub. Date Nov. 12, 1998Herein disclosed are prophylactic/therapeutic agents for atherosclerosis containing a compound of general formula (1): wherein R1 represents a hydrogen atom or an acyl group, R2 represents a lower alkyl group, R3 represents a hydrogen atom or a lower alkyl group, and R4, R5 and R6 represent a hydrogen atom, an alkyl group, an alkenyl group, an alkynyl group or an aryl group, or R2 and R4 together with the oxygen atom may form a furan or dihydrofuran ring, or R5 and R6 may combine to form a cycloalkyl group or a heterosubstituted cycloalkyl group in which one or more methylene groups of the cycloalkyl group are replaced by oxygen, sulfur or alkyl-substituted nitrogen atoms, a possible optically active isomer or a pharmaceutically acceptable salt thereof, as an active ingredient.

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