Cas 100669-22-5,(1aR,4aS,8aS)-3,4a,8,8-Tetramethyl-octahydro-cyclopropa[d]naphthalen-2-one

100669-22-5

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Basic information

Product Name: (1aR,4aS,8aS)-3,4a,8,8-Tetramethyl-octahydro-cyclopropa[d]naphthalen-2-one
Synonyms:
CAS NO:100669-22-5
Molecular Formula:
Molecular Weight: 220.355
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: (1aR,4aS,8aS)-3,4a,8,8-Tetramethyl-octahydro-cyclopropa[d]naphthalen-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (1aR,4aS,8aS)-3,4a,8,8-Tetramethyl-octahydro-cyclopropa[d]naphthalen-2-one(100669-22-5)
EPA Substance Registry System: (1aR,4aS,8aS)-3,4a,8,8-Tetramethyl-octahydro-cyclopropa[d]naphthalen-2-one(100669-22-5)

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: 100669-22-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 100669-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,6 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100669-22:
(8*1)+(7*0)+(6*0)+(5*6)+(4*6)+(3*9)+(2*2)+(1*2)=95
95 % 10 = 5
So 100669-22-5 is a valid CAS Registry Number.

100669-22-5Upstream product

470-40-6 thujopsene

100669-22-5Downstream Products

100669-22-5Relevant academic research and scientific papers

DICYANOANTHRACENE-SENSITIZED PHOTOOXYGENATION OF THUJOPSENE

Hatsui, Toshihide,Suzuki, Nobumasa,Takeshita, Hitoshi

, p. 639 - 642 (2007/10/02)

9,10-Dicyanoanthracene-sensitized photooxygenation of thujopsene proceeded by singlet oxygen, but the reaction with added biphenyl caused an electron transfer and produced a novel product which has no longer possessed the cyclopropane ring.The ring cleavage is best explained in terms of intermediary formation of a radical cation.

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