Cas 1609076-53-0,2-{(4-chlorophenyl)[(4-isopropylphenyl)thio]methyl}-3-hydroxy-5,5-dimethylcyclohex-2-enone

1609076-53-0

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Basic information

Product Name: 2-{(4-chlorophenyl)[(4-isopropylphenyl)thio]methyl}-3-hydroxy-5,5-dimethylcyclohex-2-enone
Synonyms: 2-{(4-chlorophenyl)[(4-isopropylphenyl)thio]methyl}-3-hydroxy-5,5-dimethylcyclohex-2-enone
CAS NO:1609076-53-0
Molecular Formula:
Molecular Weight: 414.996
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-{(4-chlorophenyl)[(4-isopropylphenyl)thio]methyl}-3-hydroxy-5,5-dimethylcyclohex-2-enone(CAS DataBase Reference)
NIST Chemistry Reference: 2-{(4-chlorophenyl)[(4-isopropylphenyl)thio]methyl}-3-hydroxy-5,5-dimethylcyclohex-2-enone(1609076-53-0)
EPA Substance Registry System: 2-{(4-chlorophenyl)[(4-isopropylphenyl)thio]methyl}-3-hydroxy-5,5-dimethylcyclohex-2-enone(1609076-53-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1609076-53-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609076-53-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,0,7 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1609076-53:
(9*1)+(8*6)+(7*0)+(6*9)+(5*0)+(4*7)+(3*6)+(2*5)+(1*3)=170
170 % 10 = 0
So 1609076-53-0 is a valid CAS Registry Number.

1609076-53-0Upstream product

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1609076-53-0Relevant academic research and scientific papers

Three-component reactions of aromatic aldehydes and two different nucleophiles and their leaving ability-determined downstream conversions of the products

Li, Minghao,Taheri, Amir,Liu, Meng,Sun, Shaohuan,Gu, Yanlong

, p. 537 - 556 (2014)

Many three-component reactions of aromatic aldehydes with activated methylene derivatives and an associated nucleophile have been developed by using l-proline as the catalyst. Nucleophiles, such as indoles, thiophenols, mercaptans, 2-methylfuran and benze

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