Cas 595604-49-2,Carbonic acid, ethyl (2E)-3-[2-(methoxymethoxy)phenyl]-1-(trifluoromethyl)-2-propenyl ester

595604-49-2

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Basic information

Product Name: Carbonic acid, ethyl (2E)-3-[2-(methoxymethoxy)phenyl]-1-(trifluoromethyl)-2-propenyl ester
Synonyms:
CAS NO:595604-49-2
Molecular Formula: C15H17F3O5
Molecular Weight: 334.292
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: Carbonic acid, ethyl (2E)-3-[2-(methoxymethoxy)phenyl]-1-(trifluoromethyl)-2-propenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbonic acid, ethyl (2E)-3-[2-(methoxymethoxy)phenyl]-1-(trifluoromethyl)-2-propenyl ester(595604-49-2)
EPA Substance Registry System: Carbonic acid, ethyl (2E)-3-[2-(methoxymethoxy)phenyl]-1-(trifluoromethyl)-2-propenyl ester(595604-49-2)

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: 595604-49-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 595604-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,5,6,0 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 595604-49:
(8*5)+(7*9)+(6*5)+(5*6)+(4*0)+(3*4)+(2*4)+(1*9)=192
192 % 10 = 2
So 595604-49-2 is a valid CAS Registry Number.

595604-49-2Upstream product

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595604-49-2Relevant academic research and scientific papers

The polar effect on the regiochemistry of nucleophilic substitution of trifluoromethylated π-allylpalladium complex

Okano, Takashi,Matsubara, Hiroyoshi,Kusukawa, Takahiro,Fujita, Makoto

, p. 43 - 48 (2007/10/03)

Allylic nucleophilic substitution of trifluoromethyl-group substituted cinnamyl carbonate with diethyl malonate anion in the presence of palladium complex catalyst gave regio- and stereoselectively the SN2′ product. The regiochemistry caused by

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