Cas 7416-01-5,3',4'-dihydrospiro[cyclohexane-1,2'-(1'H)-naphthalen]-1'-one

7416-01-5

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Basic information

Product Name: 3',4'-dihydrospiro[cyclohexane-1,2'-(1'H)-naphthalen]-1'-one
Synonyms: 3',4'-dihydrospiro[cyclohexane-1,2'-(1'H)-naphthalen]-1'-one
CAS NO:7416-01-5
Molecular Formula:
Molecular Weight: 214.307
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: 3',4'-dihydrospiro[cyclohexane-1,2'-(1'H)-naphthalen]-1'-one(CAS DataBase Reference)
NIST Chemistry Reference: 3',4'-dihydrospiro[cyclohexane-1,2'-(1'H)-naphthalen]-1'-one(7416-01-5)
EPA Substance Registry System: 3',4'-dihydrospiro[cyclohexane-1,2'-(1'H)-naphthalen]-1'-one(7416-01-5)

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: 7416-01-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 7416-01-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,1 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7416-01:
(6*7)+(5*4)+(4*1)+(3*6)+(2*0)+(1*1)=85
85 % 10 = 5
So 7416-01-5 is a valid CAS Registry Number.

7416-01-5Upstream product

495414-07-8 1-(2-iodophenethyl)cyclohexanecarbonitrile

7416-01-5Downstream Products

7413-07-2 8,9-dihydro-6H-benzocycloheptanespiro-6,1'-cyclopentane-5-one oxime

7416-01-5Relevant academic research and scientific papers

Carbopalladation of nitriles: Synthesis of benzocyclic ketones and cyclopentenones via Pd-catalyzed cyclization of ω-(2-iodoaryl)alkanenitriles and related compounds

Pletnev, Alexandre A.,Larock, Richard C.

, p. 9428 - 9438 (2007/10/03)

An efficient procedure for the synthesis of 2,2-disubstituted benzocyclic ketones by intramolecular carbopalladation of nitriles has been developed. The cyclization of substituted 3-(2-iodoaryl)-propanenitriles affords indanones in high yields. The reaction is compatible with a wide variety of functional groups. This methodology has been extended to the synthesis of tetralones and cyclopentenones.

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