56421-90-0 Usage
Uses
Used in Flavoring Industry:
2-[(4-CHLOROPHENYL)SULFANYL]-2-METHYLPROPANAL is used as a flavoring agent for its distinctive garlic-like aroma, enhancing the taste and appeal of food products such as beverages and baked goods.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-[(4-CHLOROPHENYL)SULFANYL]-2-METHYLPROPANAL is utilized in the production of various medications, contributing to the development of new drugs due to its unique chemical properties.
Used in Chemical Research and Development:
Due to its stability and non-reactivity, 2-[(4-CHLOROPHENYL)SULFANYL]-2-METHYLPROPANAL is considered a valuable compound in chemical research and development, where it may be employed in the synthesis of other complex organic compounds or as a reagent in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 56421-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,2 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56421-90:
(7*5)+(6*6)+(5*4)+(4*2)+(3*1)+(2*9)+(1*0)=120
120 % 10 = 0
So 56421-90-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClOS/c1-10(2,7-12)13-9-5-3-8(11)4-6-9/h3-7H,1-2H3
56421-90-0Relevant academic research and scientific papers
REACTIONS OF HALOGEN-CONTAINING O-SILYLATED ENOLATES. VII. REACTIONS OF HALOGEN-CONTAINING O-SILYLATED ENOLATES WITH SULFENYL CHLORIDES
Shchepin, V. V.,Petukhova, I. Yu.,Nedugov, A. N.,Vakhrin, M. I.
, p. 1510 - 1514 (2007/10/02)
Reactions of halogen-containing O-silylated enolates with arenesulfenyl chlorides lead to aldehydes and ketones containing halogen atoms and an arylthio group in the α position.Reaction between these reactants is accelerated by change from electron-acceptor to electron-donor substituents both in the silyl ether and in the sulfenyl chloride and by the use of polar solvents.For silyl ethers of enols of aldehydes reaction with sulfenyl chlorides proceeds through the stage of the formation of a halogen-containing 2-arylthio-1-halo-1-(trimethylsiloxy)alkane, which is an intermediate 1,2-addition product.
