Cas 851768-19-9,Benzoic acid, 2,4,6-trimethyl-, 2-[(trifluoroacetyl)oxy]-1-[[(trifluoroacetyl)oxy]methyl]ethyl ester

851768-19-9

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Basic information

Product Name: Benzoic acid, 2,4,6-trimethyl-, 2-[(trifluoroacetyl)oxy]-1-[[(trifluoroacetyl)oxy]methyl]ethyl ester
Synonyms:
CAS NO:851768-19-9
Molecular Formula: C17H16F6O6
Molecular Weight: 430.301
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: Benzoic acid, 2,4,6-trimethyl-, 2-[(trifluoroacetyl)oxy]-1-[[(trifluoroacetyl)oxy]methyl]ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid, 2,4,6-trimethyl-, 2-[(trifluoroacetyl)oxy]-1-[[(trifluoroacetyl)oxy]methyl]ethyl ester(851768-19-9)
EPA Substance Registry System: Benzoic acid, 2,4,6-trimethyl-, 2-[(trifluoroacetyl)oxy]-1-[[(trifluoroacetyl)oxy]methyl]ethyl ester(851768-19-9)

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: 851768-19-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 851768-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,7,6 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 851768-19:
(8*8)+(7*5)+(6*1)+(5*7)+(4*6)+(3*8)+(2*1)+(1*9)=199
199 % 10 = 9
So 851768-19-9 is a valid CAS Registry Number.

851768-19-9Upstream product

851768-19-9Downstream Products

133232-29-8 2-O-(2,4,6-trimethylbenzoyl)glycerol

851768-19-9Relevant academic research and scientific papers

Regioselective opening of an oxirane system with trifluoroacetic anhydride. A general method for the synthesis of 2-monoacyl- and 1,3-symmetrical triacylglycerols

Stamatov, Stephan D.,Stawinski, Jacek

, p. 3659 - 3669 (2007/10/03)

A trifluoroacetic anhydride-catalyzed opening of the oxirane system of glycidyl esters with a simultaneous migration of the acyl group provides a new, efficient entry to either 2-monoacylglycerols (2-MAG) or 1,3-symmetrical triglycerides (1,3-STG) as potential prodrug frameworks.

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