Cas 87648-98-4,(3aR,6S,7aR)-2-Benzyloxy-3-isopropenyl-2-methyl-1,2,3,6,7,7a-hexahydro-3a,6-methano-indene

87648-98-4

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Basic information

Product Name: (3aR,6S,7aR)-2-Benzyloxy-3-isopropenyl-2-methyl-1,2,3,6,7,7a-hexahydro-3a,6-methano-indene
Synonyms:
CAS NO:87648-98-4
Molecular Formula:
Molecular Weight: 294.437
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,6S,7aR)-2-Benzyloxy-3-isopropenyl-2-methyl-1,2,3,6,7,7a-hexahydro-3a,6-methano-indene(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,6S,7aR)-2-Benzyloxy-3-isopropenyl-2-methyl-1,2,3,6,7,7a-hexahydro-3a,6-methano-indene(87648-98-4)
EPA Substance Registry System: (3aR,6S,7aR)-2-Benzyloxy-3-isopropenyl-2-methyl-1,2,3,6,7,7a-hexahydro-3a,6-methano-indene(87648-98-4)

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: 87648-98-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 87648-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,4 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87648-98:
(7*8)+(6*7)+(5*6)+(4*4)+(3*8)+(2*9)+(1*8)=194
194 % 10 = 4
So 87648-98-4 is a valid CAS Registry Number.

87648-98-4Upstream product

87648-92-8 (1-Allyl-2-cyclopenta-1,3-dienyl-1,3-dimethyl-but-3-enyloxymethyl)-benzene

87648-98-4Downstream Products

87648-98-4Relevant academic research and scientific papers

SYNTHESIS OF POLYQUINANES I: INTRAMOLECULAR DIELS-ALDER REACTION

Sternbach, Daniel D.,Hughes, Jeffrey W.,Burdi, Douglas F.,Forstot, Robert M.

, p. 3295 - 3298 (1983)

The intramolecular Diels-Alder reaction of several substituted cyclopentadienes to funcionalized tricyclic products, suitable for the transformation to polyquinane natural products, is described.

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