Cas 600168-58-9,1,3,2-Dioxaborolane, 2-[4,5-dihydro-5-phenyl-7-(trifluoromethyl)-2-oxepinyl]-4,4,5,5-tetrameth yl-

600168-58-9

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Basic information

Product Name: 1,3,2-Dioxaborolane, 2-[4,5-dihydro-5-phenyl-7-(trifluoromethyl)-2-oxepinyl]-4,4,5,5-tetrameth yl-
Synonyms:
CAS NO:600168-58-9
Molecular Formula: C19H22BF3O3
Molecular Weight: 366.188
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: 1,3,2-Dioxaborolane, 2-[4,5-dihydro-5-phenyl-7-(trifluoromethyl)-2-oxepinyl]-4,4,5,5-tetrameth yl-(CAS DataBase Reference)
NIST Chemistry Reference: 1,3,2-Dioxaborolane, 2-[4,5-dihydro-5-phenyl-7-(trifluoromethyl)-2-oxepinyl]-4,4,5,5-tetrameth yl-(600168-58-9)
EPA Substance Registry System: 1,3,2-Dioxaborolane, 2-[4,5-dihydro-5-phenyl-7-(trifluoromethyl)-2-oxepinyl]-4,4,5,5-tetrameth yl-(600168-58-9)

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: 600168-58-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 600168-58-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,0,1,6 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 600168-58:
(8*6)+(7*0)+(6*0)+(5*1)+(4*6)+(3*8)+(2*5)+(1*8)=119
119 % 10 = 9
So 600168-58-9 is a valid CAS Registry Number.

600168-58-9Upstream product

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600168-58-9Relevant academic research and scientific papers

A facile approach to 2-CF3-substituted seven-membered oxacycles via stereoselective preparation and cope rearrangement of 2-CF 3-cis-2,3-bis(alkenyl)oxiranes

Shimizu, Masaki,Fujimoto, Takuya,Liu, Xinyu,Hiyama, Tamejiro

, p. 438 - 439 (2004)

Stereoselective preparation and Cope rearrangement of 2-CF 3-substituted cis-2,3-bis(alkenyl)oxiranes provides a convenient route to a diverse of 2-CF3-4,5-dihydrooxepins. The reaction sequence followed by reduction or oxidation provides 2-CF3-substituted oxepanes or oxepins, respectively.

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