Cas 137200-30-7,(Z)-(4aS,8aR)-4a-Methyl-4,4a,5,8,8a,9,10,11,12,12a-decahydro-3H-dibenzo[a,c]cycloocten-2-one

137200-30-7

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Basic information

Product Name: (Z)-(4aS,8aR)-4a-Methyl-4,4a,5,8,8a,9,10,11,12,12a-decahydro-3H-dibenzo[a,c]cycloocten-2-one
Synonyms:
CAS NO:137200-30-7
Molecular Formula:
Molecular Weight: 244.377
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: (Z)-(4aS,8aR)-4a-Methyl-4,4a,5,8,8a,9,10,11,12,12a-decahydro-3H-dibenzo[a,c]cycloocten-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-(4aS,8aR)-4a-Methyl-4,4a,5,8,8a,9,10,11,12,12a-decahydro-3H-dibenzo[a,c]cycloocten-2-one(137200-30-7)
EPA Substance Registry System: (Z)-(4aS,8aR)-4a-Methyl-4,4a,5,8,8a,9,10,11,12,12a-decahydro-3H-dibenzo[a,c]cycloocten-2-one(137200-30-7)

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: 137200-30-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 137200-30-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,2,0 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 137200-30:
(8*1)+(7*3)+(6*7)+(5*2)+(4*0)+(3*0)+(2*3)+(1*0)=87
87 % 10 = 7
So 137200-30-7 is a valid CAS Registry Number.

137200-30-7Upstream product

137200-05-6 (Z)-3-(1-cyclohexenyl)-4-methyl-4-<4-(trimethylsilyl)-2-butenyl>-2-cyclohexen-1-one

137200-30-7Downstream Products

137200-30-7Relevant academic research and scientific papers

Cyclooctane or Cyclohexane Annulations Based on Intramolecular Additions of Allylsilanes to Conjugated Dienones

Majetich, George,Hull, Kenneth,Casares, Ada M.,Khetani, Vikram

, p. 3958 - 3973 (1991)

The scope and limitations of alkenyl dienone cyclizations for the formation of fused cyclooctane or cyclohexane systems are described.

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