Cas 170745-08-1,4-tert-Butyl-cyclohex-1-enecarboxylic acid 2-iodo-4-methyl-phenyl ester

170745-08-1

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Basic information

Product Name: 4-tert-Butyl-cyclohex-1-enecarboxylic acid 2-iodo-4-methyl-phenyl ester
Synonyms: 4-tert-Butyl-cyclohex-1-enecarboxylic acid 2-iodo-4-methyl-phenyl ester
CAS NO:170745-08-1
Molecular Formula:
Molecular Weight: 398.284
EINECS: N/A
Product Categories: N/A
Mol File: 170745-08-1.mol
Article Data: 1

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: 4-tert-Butyl-cyclohex-1-enecarboxylic acid 2-iodo-4-methyl-phenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-tert-Butyl-cyclohex-1-enecarboxylic acid 2-iodo-4-methyl-phenyl ester(170745-08-1)
EPA Substance Registry System: 4-tert-Butyl-cyclohex-1-enecarboxylic acid 2-iodo-4-methyl-phenyl ester(170745-08-1)

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: 170745-08-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 170745-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,7,4 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 170745-08:
(8*1)+(7*7)+(6*0)+(5*7)+(4*4)+(3*5)+(2*0)+(1*8)=131
131 % 10 = 1
So 170745-08-1 is a valid CAS Registry Number.

170745-08-1Upstream product

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170745-08-1Relevant articles and documents

Palladium-catalyzed selective carbonylation of vinyl triflates in the presence of 2-iodophenols: A new route to 3-spiro-fused benzofuran-2(3H)-ones

Anacardio,Arcadi,D'Anniballe,Marinelli

, p. 831 - 836 (1995)

A convenient synthesis of 3-spiro-fused benzofuran-2(3H)-ones via palladium-catalyzed chemoselective carbonylation of vinyl triflates in the presence of o-iodophenols, followed by regioselective intramolecular Heck reaction, is described.

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