Cas 139599-43-2,(3aR,5aS,8aS,8bS)-2-Ethoxy-5a-methyl-6-oxo-decahydro-indeno[5,4-b]furan-7-carbonitrile

139599-43-2

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Basic information

Product Name: (3aR,5aS,8aS,8bS)-2-Ethoxy-5a-methyl-6-oxo-decahydro-indeno[5,4-b]furan-7-carbonitrile
Synonyms:
CAS NO:139599-43-2
Molecular Formula:
Molecular Weight: 263.337
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: (3aR,5aS,8aS,8bS)-2-Ethoxy-5a-methyl-6-oxo-decahydro-indeno[5,4-b]furan-7-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,5aS,8aS,8bS)-2-Ethoxy-5a-methyl-6-oxo-decahydro-indeno[5,4-b]furan-7-carbonitrile(139599-43-2)
EPA Substance Registry System: (3aR,5aS,8aS,8bS)-2-Ethoxy-5a-methyl-6-oxo-decahydro-indeno[5,4-b]furan-7-carbonitrile(139599-43-2)

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: 139599-43-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 139599-43-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,5,9 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 139599-43:
(8*1)+(7*3)+(6*9)+(5*5)+(4*9)+(3*9)+(2*4)+(1*3)=182
182 % 10 = 2
So 139599-43-2 is a valid CAS Registry Number.

139599-43-2Upstream product

139599-56-7 (3aR,5aS,8aS,8bS)-6-[3-Cyano-1-methyl-prop-(E)-ylidene]-2-ethoxy-5a-methyl-decahydro-indeno[5,4-b]furan-7-carbonitrile

139599-43-2Downstream Products

139599-43-2Relevant academic research and scientific papers

Multiple Carbon Bond Formation via the Radical Cyclization of Cycloalkenol Acetals. Application to trans Hydrindan Steroid Precursors

Stork, Gilbert,Franklin, Paul J.

, p. 275 - 284 (2007/10/02)

The cyclization of the α-iodo mixed acetals derived from properly substituted cyclohexanols, a process which has already been shown to permit the stereoselective and regioselective introduction of a different carbon chain at each of the termini of the all

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