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67522-25-2

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67522-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67522-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,2 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67522-25:
(7*6)+(6*7)+(5*5)+(4*2)+(3*2)+(2*2)+(1*5)=132
132 % 10 = 2
So 67522-25-2 is a valid CAS Registry Number.

67522-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,5,5-tetramethylcyclopentene-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3,3,5,5-Tetramethyl-cyclopent-1-encarbonsaeure

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:67522-25-2 SDS

67522-25-2Downstream Products

67522-25-2Relevant articles and documents

Formation of 1,3-Oxaselenoles via Pummerer Reaction in Selenium Dioxide Oxidation of Cyclic 1,2- and 1,3-Diketones, and the Preparation of 1,5,5-Trimethyl-7-selenabicycloheptane-2,3-dione

Laitalainen, Tarja,Simonen, Tapio,Kivekaes, Raikko,Klinga, Martti

, p. 333 - 340 (2007/10/02)

4,5,6,7-Tetrahydro-4',4',6,6-tetramethylspiro-2',4,6'-trione and related 1,3-oxaselenole derivatives, and not the previously reported selenoxides of type (1), are formed in the selenium dioxide oxidation of cyclohexane-1,3-diones.The structural assignments were made on the basis of n.m.r. spectroscopy, and in the case of (5), X-ray analysis was undertaken.Oxidation of 3,3,5,5-tetramethylcyclohexane-1,2-dione with selenium dioxide yielded the bis-selenide (9) and the 1,3-oxaselenole (10) along with the usual oxidation products, whereas the oxidation of 3,5,5-trimethylcyclohexane-1,2-dione gave the title, bridged selenabicyclic compound.

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