62750-60-1 Usage
Category
Sulfonylphenyl derivatives
This compound belongs to a group of chemical compounds that have a sulfonyl group (-SO2) attached to a phenyl ring (a six-membered ring with alternating single and double carbon-carbon bonds).
Family
Benzene and substituted derivatives
It is part of a larger family of compounds based on the benzene structure, which is a six-membered ring with alternating single and double carbon-carbon bonds, and has been modified by adding other functional groups.
Physical appearance
White solid
The compound appears as a white solid, which is a common physical form for many organic compounds.
Molecular weight
322.4 g/mol
The relative molecular mass (molecular weight) of 2-(2-[2-(prop-1-en-2-yl)phenyl]sulfonylphenyl)propan-2-ol is 322.4 grams per mole.
6. Usage in organic synthesis and pharmaceutical research
Due to its unique chemical structure and properties, this compound is commonly used in the field of organic synthesis and pharmaceutical research to create new drugs, medicines, and industrial chemicals.
Primary application
Development of new drugs and medicines
One of the main applications of this compound is in the development of new pharmaceutical products, as its unique structure may lead to the creation of novel therapeutic agents.
8. Production of various industrial chemicals
The compound is also used in the production of other industrial chemicals, highlighting its versatility and importance in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 62750-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,5 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62750-60:
(7*6)+(6*2)+(5*7)+(4*5)+(3*0)+(2*6)+(1*0)=121
121 % 10 = 1
So 62750-60-1 is a valid CAS Registry Number.
62750-60-1Relevant articles and documents
Unexpected conversions of selected heteroorganic compounds
Drabowicz, Jozef
, p. 437 - 442 (2007/10/03)
A few unexpected conversions of selected heteroorganic compounds are described, including the formation of N-sulfonyl sulfenamide derivatives and the mixed phosphinyl-sulfenyl anhydrides in the reactions of sulfinyl chlorides with α-phenylethylamine or t-butyl-phenylphosphine oxide, respectively. Unexpected reactions of the ortho hydroxyalkyl-substituted diaryl sulfoxides and hypervalent sulfur and selenium derivatives, induced by triphenylphosphine, are also presented. Attempts to rationalize the observed reaction courses are briefly discussed.
