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76800-28-7

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76800-28-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76800-28-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,0 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76800-28:
(7*7)+(6*6)+(5*8)+(4*0)+(3*0)+(2*2)+(1*8)=137
137 % 10 = 7
So 76800-28-7 is a valid CAS Registry Number.

76800-28-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5'-dichloro-2,2'-dihydroxy-3,3'-dimethylbiphenyl

1.2 Other means of identification

Product number -
Other names 5,5'-dichloro-3,3'-dimethyl-2,2'-biphenol

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:76800-28-7 SDS

76800-28-7Downstream Products

76800-28-7Relevant articles and documents

Reactions of Alkyl-lithium Compounds with Aryl Halides

Huddle, Penelope A.,Perold, Guido W.

, p. 2617 - 2625 (2007/10/02)

Reation of methyl-lithium with tribromophenols and with other aryl polyhalides leads directly to bi- and tri-aryl products. para-Substituents (Y) of 2,6-dibromo-4-Y-phenols promote arylation of substrates by their own lithiation products as Y becomes more electron-withdrawing.An aryne epoxide is not an intermediate in these reactions. 2,4,6-Tribromo-Z-benzenes react to form coupling products when Z can co-ordinate to an introduced ortho-lithium atom or when Z can be directly lithiated.Dimeric aggregation of the organolithium intermediates occurs so as to favor coupling to halogenated substrates.Both polar (ionic) and free-radical pathways are involved.

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