Cas 366002-39-3,trifluoro-methanesulfonic acid 3-[2,2-difluoro-1-(2-methoxy-ethoxymethoxy)-vinyl]-phenyl ester

366002-39-3

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Basic information

Product Name: trifluoro-methanesulfonic acid 3-[2,2-difluoro-1-(2-methoxy-ethoxymethoxy)-vinyl]-phenyl ester
Synonyms: trifluoro-methanesulfonic acid 3-[2,2-difluoro-1-(2-methoxy-ethoxymethoxy)-vinyl]-phenyl ester
CAS NO:366002-39-3
Molecular Formula:
Molecular Weight: 392.301
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: trifluoro-methanesulfonic acid 3-[2,2-difluoro-1-(2-methoxy-ethoxymethoxy)-vinyl]-phenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: trifluoro-methanesulfonic acid 3-[2,2-difluoro-1-(2-methoxy-ethoxymethoxy)-vinyl]-phenyl ester(366002-39-3)
EPA Substance Registry System: trifluoro-methanesulfonic acid 3-[2,2-difluoro-1-(2-methoxy-ethoxymethoxy)-vinyl]-phenyl ester(366002-39-3)

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: 366002-39-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 366002-39-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,6,0,0 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 366002-39:
(8*3)+(7*6)+(6*6)+(5*0)+(4*0)+(3*2)+(2*3)+(1*9)=123
123 % 10 = 3
So 366002-39-3 is a valid CAS Registry Number.

366002-39-3Upstream product

366002-39-3Downstream Products

366002-54-2 2-{3-[2,2-difluoro-1-(2-methoxy-ethoxymethoxy)-vinyl]-phenyl}-thiophene

366002-39-3Relevant academic research and scientific papers

Generating diversity in difluoromethyl ketone derivatives

DeBoos, Gareth A.,Fullbrook, Jeremy J.,Percy, Jonathan M.

, p. 2859 - 2861 (2001)

(equation presented) Two consecutive palladium-catalyzed coupling reactions from a readily available difluoroenol stannane set the stage for the synthesis of a range of difluoro-and halodifluoromethyl ketones upon a variable aryl template.

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