Cas 177981-77-0,4,4-Dimethoxy-3-oxo-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

177981-77-0

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Basic information

Product Name: 4,4-Dimethoxy-3-oxo-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
Synonyms: 4,4-Dimethoxy-3-oxo-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
CAS NO:177981-77-0
Molecular Formula:
Molecular Weight: 300.395
EINECS: N/A
Product Categories: N/A
Mol File: 177981-77-0.mol
Article Data: 1

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: 4,4-Dimethoxy-3-oxo-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4,4-Dimethoxy-3-oxo-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(177981-77-0)
EPA Substance Registry System: 4,4-Dimethoxy-3-oxo-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(177981-77-0)

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: 177981-77-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 177981-77-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,9,8 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 177981-77:
(8*1)+(7*7)+(6*7)+(5*9)+(4*8)+(3*1)+(2*7)+(1*7)=200
200 % 10 = 0
So 177981-77-0 is a valid CAS Registry Number.

177981-77-0Upstream product

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177981-77-0Relevant articles and documents

Enantioselective syntheses and resolution of the key White intermediate for the synthesis of trisporic acids

Bacigaluppo, Jose A.,Colombo, Maria I.,Preite, Marcelo D.,Zinczuk, Juan,Ruveda, Edmundo A.,Sieler, Joachim

, p. 1041 - 1057 (2007/10/03)

Two asymmetric syntheses of the alkylated cyclohexenone carboxylic acid moiety, the key White intermediate (4a), of trisporic acids A, B and C are described. The syntheses feature a Michael addition in tandem with an aldol condensation as the central step

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