Cas 79091-71-7,6-Acetyl-1-(4-chloro-phenylsulfanyl)-3-methyl-4-oxo-cyclohex-2-enecarboxylic acid ethyl ester

79091-71-7

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Basic information

Product Name: 6-Acetyl-1-(4-chloro-phenylsulfanyl)-3-methyl-4-oxo-cyclohex-2-enecarboxylic acid ethyl ester
Synonyms: 6-Acetyl-1-(4-chloro-phenylsulfanyl)-3-methyl-4-oxo-cyclohex-2-enecarboxylic acid ethyl ester
CAS NO:79091-71-7
Molecular Formula:
Molecular Weight: 366.865
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: 6-Acetyl-1-(4-chloro-phenylsulfanyl)-3-methyl-4-oxo-cyclohex-2-enecarboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 6-Acetyl-1-(4-chloro-phenylsulfanyl)-3-methyl-4-oxo-cyclohex-2-enecarboxylic acid ethyl ester(79091-71-7)
EPA Substance Registry System: 6-Acetyl-1-(4-chloro-phenylsulfanyl)-3-methyl-4-oxo-cyclohex-2-enecarboxylic acid ethyl ester(79091-71-7)

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: 79091-71-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79091-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,9 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79091-71:
(7*7)+(6*9)+(5*0)+(4*9)+(3*1)+(2*7)+(1*1)=157
157 % 10 = 7
So 79091-71-7 is a valid CAS Registry Number.

79091-71-7Upstream product

79091-71-7Downstream Products

79091-60-4 ethyl 2-acetyl-4-hydroxy-5-methyl benzoate

79091-71-7Relevant academic research and scientific papers

Model Studies on the Synthesis of Milbemycin β3

Attwood, Stephen V.,Barrett, Anthony G. M.,Florent, Jean-Claude

, p. 556 - 557 (1981)

2,4-Di(lithio-oxy)penta-1,3-diene and 2,4-di(lithio-oxy)-3-methylpenta-1,3-diene condensed with tetrahydropyran-2-one to give 2-methyl- and 2,3-dimethyl-1,7-dioxaspiroundec-2-en-4-one; subsequent reduction gave the derived alcohols (LiAlH4) and 2,3-d

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