92189-66-7 Usage
Explanation
The compound is composed of 13 carbon atoms, 11 hydrogen atoms, 1 bromine atom, and 2 oxygen atoms.
Explanation
The compound has a carbonyl group (C=O) bonded to two carbon atoms, which classifies it as a ketone.
Explanation
The compound features a naphthalene ring, which is a fused pair of benzene rings, with a bromine atom at the 5-position and a methoxy group at the 6-position.
Explanation
Due to its unique structure and reactivity, the compound is used as a starting material for the synthesis of various pharmaceuticals and organic compounds.
Explanation
The compound's distinct structure and reactivity make it a useful intermediate in the development of new chemical entities and pharmaceutical agents.
Explanation
The solubility of the compound in different solvents is not mentioned in the provided information.
Explanation
The stability of the compound under various conditions is not mentioned in the provided information.
Explanation
The potential hazards or safety concerns associated with the compound are not mentioned in the provided information.
Functional Group
Ketone
Structure
Naphthalene ring with a bromine and methoxy group
Application
Building block in pharmaceuticals and organic compounds
Reactivity
Valuable tool in organic chemistry research and drug development
Solubility
Not specified in the material provided
Stability
Not specified in the material provided
Hazards
Not specified in the material provided
Check Digit Verification of cas no
The CAS Registry Mumber 92189-66-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,8 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92189-66:
(7*9)+(6*2)+(5*1)+(4*8)+(3*9)+(2*6)+(1*6)=157
157 % 10 = 7
So 92189-66-7 is a valid CAS Registry Number.
92189-66-7Relevant articles and documents
Intermediates for preparing optically active carboxylic acids
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, (2008/06/13)
A process is described for preparing optically active alpha-arylalkanoic acids consisting of rearranging an optically active ketal of formula STR1 in which the substituents have the meaning given in the description of the invention.
