Cas 6252-26-2,Dodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran

6252-26-2

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Basic information

Product Name: Dodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran
Synonyms: Dodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran
CAS NO:6252-26-2
Molecular Formula: C18H32O
Molecular Weight: 264.45
EINECS: N/A
Product Categories: N/A
Mol File: 6252-26-2.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: Dodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran(CAS DataBase Reference)
NIST Chemistry Reference: Dodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran(6252-26-2)
EPA Substance Registry System: Dodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran(6252-26-2)

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: 6252-26-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 6252-26-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,5 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6252-26:
(6*6)+(5*2)+(4*5)+(3*2)+(2*2)+(1*6)=82
82 % 10 = 2
So 6252-26-2 is a valid CAS Registry Number.

6252-26-2Upstream product

587888-42-4 5E,9E-farnesyl rac-acet-2-ol

6252-26-2Downstream Products

6252-26-2Relevant academic research and scientific papers

Polyene cyclizations using mercury(II) triflate-N,N-dimethylaniline complex-participation by internal nucleophiles

Gopalan,Prieto,Mueller,Peters

, p. 1679 - 1682 (2007/10/02)

The cyclization of a number of functionalized polyenes with mercuric triflate-N,N-dimethylaniline complex (Nishizawa's reagent) to give bicyclic or tricyclic products has been studied. Suitably positioneal internal nucleophiles, such as carbonyl, hydroxy and β-ketoester groups were found to participate to varying extent, in the termination of these cyclizations.

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