Cas 195060-63-0,Benzoic acid, 4-iodo-3-[[2-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl)-2 -propenyl]oxy]-, methyl ester

195060-63-0

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Basic information

Product Name: Benzoic acid, 4-iodo-3-[[2-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl)-2 -propenyl]oxy]-, methyl ester
Synonyms:
CAS NO:195060-63-0
Molecular Formula: C26H31IO3
Molecular Weight: 518.435
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: Benzoic acid, 4-iodo-3-[[2-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl)-2 -propenyl]oxy]-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid, 4-iodo-3-[[2-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl)-2 -propenyl]oxy]-, methyl ester(195060-63-0)
EPA Substance Registry System: Benzoic acid, 4-iodo-3-[[2-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl)-2 -propenyl]oxy]-, methyl ester(195060-63-0)

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: 195060-63-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 195060-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,0,6 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 195060-63:
(8*1)+(7*9)+(6*5)+(5*0)+(4*6)+(3*0)+(2*6)+(1*3)=140
140 % 10 = 0
So 195060-63-0 is a valid CAS Registry Number.

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195060-63-0Relevant academic research and scientific papers

New synthetic retinoids obtained by palladium-catalyzed tandem cyclisation-hydride capture process

Diaz, Philippe,Gendre, Fabrice,Stella, Lucien,Charpentier, Bruno

, p. 4579 - 4590 (2007/10/03)

A new series of conformationally restricted retinoids (3-aryl-3-methyl- 2,3-dihydrobenzofurans) have been prepared through a palladium-catalyzed tandem cyclisation-hydride capture. The use of enantiopure BINAP-Pd catalyst allowed asymmetric synthesis of bioactive molecules.

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