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89279-14-1

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89279-14-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89279-14-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,7 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89279-14:
(7*8)+(6*9)+(5*2)+(4*7)+(3*9)+(2*1)+(1*4)=181
181 % 10 = 1
So 89279-14-1 is a valid CAS Registry Number.

89279-14-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-o-Toluyl-p-benzoquinone, Bis(dimethyl acetal)

1.2 Other means of identification

Product number -
Other names (3,3,6,6-Tetramethoxy-cyclohexa-1,4-dienyl)-o-tolyl-methanone

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:89279-14-1 SDS

89279-14-1Downstream Products

89279-14-1Relevant articles and documents

Mechanistic Aspects of the Annelation Reactions of Benzocyclobutenedione Monoketals with Vinyllithium Reagents

Spangler, Lori A.,Swenton, John S.

, p. 1800 - 1806 (2007/10/02)

The mechanism of the annelation reaction of vinyllithium reagents with benzocyclobutenedione monoketals has been investigated.The results of these studies strongly support a mechanism involving addition of the organolithium reagent to form the lithium salt of a benzocyclobutenol followed by ring opening and cyclization to produce the tricyclic product.This reaction was examined with benzocyclobutenone and with the ethylene glycol and ethanedithiol monoketals of benzocyclobutenedione as the carbonyl components.The lithio derivatives of the bisketal of 2-bromobenzoquinone, the ethylene glycol ketal of α-bromocyclohexenone, and the ethanedithiol ketal of β-bromocyclohexenone were explored as the organometallic components.These studies have established the major mechanistic aspects and the scope of this annelation reaction.

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