Cas 76016-01-8,(1R,2R,3R,7S,8S,9aR)-2,3,8-Tribromo-7-chloro-1,4,7,9a-tetramethyl-2,3,5,6,7,8,9,9a-octahydro-1H-benzocycloheptene

76016-01-8

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Basic information

Product Name: (1R,2R,3R,7S,8S,9aR)-2,3,8-Tribromo-7-chloro-1,4,7,9a-tetramethyl-2,3,5,6,7,8,9,9a-octahydro-1H-benzocycloheptene
Synonyms:
CAS NO:76016-01-8
Molecular Formula:
Molecular Weight: 477.505
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: (1R,2R,3R,7S,8S,9aR)-2,3,8-Tribromo-7-chloro-1,4,7,9a-tetramethyl-2,3,5,6,7,8,9,9a-octahydro-1H-benzocycloheptene(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,3R,7S,8S,9aR)-2,3,8-Tribromo-7-chloro-1,4,7,9a-tetramethyl-2,3,5,6,7,8,9,9a-octahydro-1H-benzocycloheptene(76016-01-8)
EPA Substance Registry System: (1R,2R,3R,7S,8S,9aR)-2,3,8-Tribromo-7-chloro-1,4,7,9a-tetramethyl-2,3,5,6,7,8,9,9a-octahydro-1H-benzocycloheptene(76016-01-8)

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: 76016-01-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 76016-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,1 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76016-01:
(7*7)+(6*6)+(5*0)+(4*1)+(3*6)+(2*0)+(1*1)=108
108 % 10 = 8
So 76016-01-8 is a valid CAS Registry Number.

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76016-01-8Relevant academic research and scientific papers

Laurencia sesquiterpene biogenetic-type interconversions

Gonzalez,Darias,Martin,Martin,Norte,Perez,Perales,Fayos

, p. 1151 - 1154 (2007/10/02)

Several aromatic sesquiterpenes from Laurencia algae were prepared from chamigrene skeleton precursors. Chemical evidence was adduced to support a biogenetic-type scheme for the synthesis of perforenol and perforene. By means of x ray analysis the structure and absolute configuration of one of the intermediates was established.

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