Cas 854759-74-3,Benzoic acid 2-[(1S,7aS)-1-(2,2-dimethyl-propionyloxy)-7a-methyl-5-oxo-2,3,5,6,7,7a-hexahydro-1H-inden-4-yl]-ethyl ester

854759-74-3

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Basic information

Product Name: Benzoic acid 2-[(1S,7aS)-1-(2,2-dimethyl-propionyloxy)-7a-methyl-5-oxo-2,3,5,6,7,7a-hexahydro-1H-inden-4-yl]-ethyl ester
Synonyms: Benzoic acid 2-[(1S,7aS)-1-(2,2-dimethyl-propionyloxy)-7a-methyl-5-oxo-2,3,5,6,7,7a-hexahydro-1H-inden-4-yl]-ethyl ester
CAS NO:854759-74-3
Molecular Formula:
Molecular Weight: 398.499
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: Benzoic acid 2-[(1S,7aS)-1-(2,2-dimethyl-propionyloxy)-7a-methyl-5-oxo-2,3,5,6,7,7a-hexahydro-1H-inden-4-yl]-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid 2-[(1S,7aS)-1-(2,2-dimethyl-propionyloxy)-7a-methyl-5-oxo-2,3,5,6,7,7a-hexahydro-1H-inden-4-yl]-ethyl ester(854759-74-3)
EPA Substance Registry System: Benzoic acid 2-[(1S,7aS)-1-(2,2-dimethyl-propionyloxy)-7a-methyl-5-oxo-2,3,5,6,7,7a-hexahydro-1H-inden-4-yl]-ethyl ester(854759-74-3)

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: 854759-74-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 854759-74-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,4,7,5 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 854759-74:
(8*8)+(7*5)+(6*4)+(5*7)+(4*5)+(3*9)+(2*7)+(1*4)=223
223 % 10 = 3
So 854759-74-3 is a valid CAS Registry Number.

854759-74-3Upstream product

854759-74-3Downstream Products

854759-75-4 C₂₆H₃₆O₄S₂

854759-74-3Relevant academic research and scientific papers

Formal total synthesis of (+)-wortmannin using catalytic asymmetric intramolecular aldol condensation reaction

Shigehisa, Hiroki,Mizutani, Takashi,Tosaki, Shin-Ya,Ohshima, Takashi,Shibasaki, Masakatsu

, p. 5057 - 5065 (2007/10/03)

A catalytic process for the synthesis of optically active C4-substituted tetrahydroindandiones using an asymmetric intramolecular aldol condensation reaction was developed. When 30 mol% of phenylalanine and 50 mol% of pyridinium p-toluenesulfonate were us

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