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2-exo-6-exo-5,5,6-trimethylbicyclo[2.2.1]heptan-2-ol is a complex organic compound with the molecular formula C??H??O. It is a bicyclic alcohol, characterized by its unique structure with two carbon rings fused together in a 2.2.1 pattern. The compound features three methyl groups (CH?) attached to the carbon atoms at positions 5, 5, and 6, and a hydroxyl group (-OH) at the 2nd position. This specific arrangement of substituents on the bicyclic framework contributes to its distinct chemical properties and potential applications in various fields, such as pharmaceuticals, fragrances, or chemical research.

3292-04-4

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3292-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3292-04-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3292-04:
(6*3)+(5*2)+(4*9)+(3*2)+(2*0)+(1*4)=74
74 % 10 = 4
So 3292-04-4 is a valid CAS Registry Number.

3292-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-exo-6-exo-5,5,6-trimethylbicyclo[2.2.1]heptan-2-ol

1.2 Other means of identification

Product number -
Other names pseudonorborneol

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:3292-04-4 SDS

3292-04-4Upstream product

3292-04-4Relevant academic research and scientific papers

Camphene hydration catalyzed by heteropoly acids

Radbil',Kulikov,Sokolova,Kartashov,Klimanskii,Radbil',Zolin

, p. 253 - 256 (2007/10/03)

Camphene hydration catalyzed by heteropoly acids H4SiW12O40 and H3PW12O40, their advantages as catalysts in comparison with simple mineral acids, and the mechanism of the homogeneous acid-catalyzed camphene hydration in aqueous-organic solvents were studied.

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