Cas 672295-29-3,1H-Inden-1-one,2,3,3a,4,5,6-hexahydro-3a-methyl-3-(1-methylethyl)-,(3R,3aR)-rel-(9CI)

672295-29-3

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Basic information

Product Name: 1H-Inden-1-one,2,3,3a,4,5,6-hexahydro-3a-methyl-3-(1-methylethyl)-,(3R,3aR)-rel-(9CI)
Synonyms: 1H-Inden-1-one,2,3,3a,4,5,6-hexahydro-3a-methyl-3-(1-methylethyl)-,(3R,3aR)-rel-(9CI)
CAS NO:672295-29-3
Molecular Formula: C13H20O
Molecular Weight: 192.2973
EINECS: N/A
Product Categories: CYCLOPENTANE
Mol File: 672295-29-3.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1H-Inden-1-one,2,3,3a,4,5,6-hexahydro-3a-methyl-3-(1-methylethyl)-,(3R,3aR)-rel-(9CI)(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Inden-1-one,2,3,3a,4,5,6-hexahydro-3a-methyl-3-(1-methylethyl)-,(3R,3aR)-rel-(9CI)(672295-29-3)
EPA Substance Registry System: 1H-Inden-1-one,2,3,3a,4,5,6-hexahydro-3a-methyl-3-(1-methylethyl)-,(3R,3aR)-rel-(9CI)(672295-29-3)

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: 672295-29-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 672295-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,2,2,9 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 672295-29:
(8*6)+(7*7)+(6*2)+(5*2)+(4*9)+(3*5)+(2*2)+(1*9)=183
183 % 10 = 3
So 672295-29-3 is a valid CAS Registry Number.

672295-29-3Upstream product

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672295-29-3Relevant academic research and scientific papers

An Expeditious Nazarov Cyclization Strategy toward the Hydroazulene Core of Guanacastepene A

Chiu, Pauline,Li, Shuoliang

, p. 613 - 616 (2004)

(Matrix presented) The hydroazulene core of guanacastepene A has been synthesized in five steps from commercially available starting materials using a classical Nazarov cyclization to install the stereochemistry in the cyclopentanone diastereoselectively.

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