Cas 1609076-75-6,2-[(4-chlorophenyl)(1-methyl-1H-pyrrol-2-yl)methyl]-3-hydroxy-5,5-dimethylcyclohex-2-enone

1609076-75-6

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Basic information

Product Name: 2-[(4-chlorophenyl)(1-methyl-1H-pyrrol-2-yl)methyl]-3-hydroxy-5,5-dimethylcyclohex-2-enone
Synonyms: 2-[(4-chlorophenyl)(1-methyl-1H-pyrrol-2-yl)methyl]-3-hydroxy-5,5-dimethylcyclohex-2-enone
CAS NO:1609076-75-6
Molecular Formula:
Molecular Weight: 343.853
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)(1-methyl-1H-pyrrol-2-yl)methyl]-3-hydroxy-5,5-dimethylcyclohex-2-enone(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(4-chlorophenyl)(1-methyl-1H-pyrrol-2-yl)methyl]-3-hydroxy-5,5-dimethylcyclohex-2-enone(1609076-75-6)
EPA Substance Registry System: 2-[(4-chlorophenyl)(1-methyl-1H-pyrrol-2-yl)methyl]-3-hydroxy-5,5-dimethylcyclohex-2-enone(1609076-75-6)

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: 1609076-75-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609076-75-6 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, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1609076-75:
(9*1)+(8*6)+(7*0)+(6*9)+(5*0)+(4*7)+(3*6)+(2*7)+(1*5)=176
176 % 10 = 6
So 1609076-75-6 is a valid CAS Registry Number.

1609076-75-6Upstream product

1609076-75-6Downstream Products

1609076-75-6Relevant 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 (2014/05/20)

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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