Cas 102341-77-5,(3S,5S)-5-(tert-Butyl-dimethyl-silanyloxymethyl)-3-((2E,4E)-hexa-2,4-dienyl)-dihydro-furan-2-one

102341-77-5

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Basic information

Product Name: (3S,5S)-5-(tert-Butyl-dimethyl-silanyloxymethyl)-3-((2E,4E)-hexa-2,4-dienyl)-dihydro-furan-2-one
Synonyms: (3S,5S)-5-(tert-Butyl-dimethyl-silanyloxymethyl)-3-((2E,4E)-hexa-2,4-dienyl)-dihydro-furan-2-one
CAS NO:102341-77-5
Molecular Formula:
Molecular Weight: 310.509
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: (3S,5S)-5-(tert-Butyl-dimethyl-silanyloxymethyl)-3-((2E,4E)-hexa-2,4-dienyl)-dihydro-furan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3S,5S)-5-(tert-Butyl-dimethyl-silanyloxymethyl)-3-((2E,4E)-hexa-2,4-dienyl)-dihydro-furan-2-one(102341-77-5)
EPA Substance Registry System: (3S,5S)-5-(tert-Butyl-dimethyl-silanyloxymethyl)-3-((2E,4E)-hexa-2,4-dienyl)-dihydro-furan-2-one(102341-77-5)

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: 102341-77-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 102341-77-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,3,4 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 102341-77:
(8*1)+(7*0)+(6*2)+(5*3)+(4*4)+(3*1)+(2*7)+(1*7)=75
75 % 10 = 5
So 102341-77-5 is a valid CAS Registry Number.

102341-77-5Upstream product

32780-06-6 (5S)-5-(hydroxymethyl)-2-oxo-tetrahydrofuran

102341-77-5Downstream Products

102341-77-5Relevant academic research and scientific papers

A Stereochemically Controlled Intramolecular Diels-Alder Approach to the Octahydronaphthalene Fragment of Dihydromevinolin

Davidson, Alan H.,Floyd, Chris D.,Jones, Andrew J.,Myers, Peter L.

, p. 1662 - 1664 (1985)

An enantiospecific route to the octahydronaphthalenene (22) from L-glutamic acid is described: the key step is the intramolecular Diels-Alder reaction (19) to (22).

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