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30829-30-2

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30829-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30829-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,2 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30829-30:
(7*3)+(6*0)+(5*8)+(4*2)+(3*9)+(2*3)+(1*0)=102
102 % 10 = 2
So 30829-30-2 is a valid CAS Registry Number.

30829-30-2SDS

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-(chloromethylene)-2,6-di-tert-butylcyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 2,6-di-tert-butyl-4-chloromethylenecyclohexa-2,5-dienone

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:30829-30-2 SDS

30829-30-2Relevant articles and documents

Reaction of esters of PIII acids with 2,6-di-tert-butyl-4-chloromethylidenecyclohexa-2,5-dienone

Gazizov,Ismagilov,Shamsutdinova,Tarakanova,Karimova

, p. 2943 - 2947 (2017/06/05)

A reaction of PIII acid esters with 2,6-di-tert-butyl-4-chloromethylidenecyclohexa-2,5-dienone leads to the formation of phosphorylated phosphorus ylides, 3,3’,5,5’-tetra-tert-butylstilbenequinone, and diphosphorylated sterically hindered phenols. The schemes for the formation of these products through the primary key intermediates of betaine and phosphorus ylide structures were suggested.

Method for producing benzylidene derivatives

-

, (2008/06/13)

A selective and high-yield method is described for producing stereoisomeric benzylidene derivatives of the formula III: STR1 wherein R1 and R2 each independently is lower alkyl, lower alkoxy or halogen; Y is SO2, SO or CO;

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