Cas 128816-99-9,(1R,8S,11S,12S)-11-Bromo-12-(2,4-dinitro-phenylsulfanyl)-3,4,5,6-tetrafluoro-tricyclo[6.2.2.0<sup>2,7</sup>]dodeca-2<sup>(7)</sup>,3,5,9-tetraene

128816-99-9

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Basic information

Product Name: (1R,8S,11S,12S)-11-Bromo-12-(2,4-dinitro-phenylsulfanyl)-3,4,5,6-tetrafluoro-tricyclo[6.2.2.0^2,7]dodeca-2⁽⁷⁾,3,5,9-tetraene
Synonyms:
CAS NO:128816-99-9
Molecular Formula:
Molecular Weight: 505.244
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: (1R,8S,11S,12S)-11-Bromo-12-(2,4-dinitro-phenylsulfanyl)-3,4,5,6-tetrafluoro-tricyclo[6.2.2.0^2,7]dodeca-2⁽⁷⁾,3,5,9-tetraene(CAS DataBase Reference)
NIST Chemistry Reference: (1R,8S,11S,12S)-11-Bromo-12-(2,4-dinitro-phenylsulfanyl)-3,4,5,6-tetrafluoro-tricyclo[6.2.2.0^2,7]dodeca-2⁽⁷⁾,3,5,9-tetraene(128816-99-9)
EPA Substance Registry System: (1R,8S,11S,12S)-11-Bromo-12-(2,4-dinitro-phenylsulfanyl)-3,4,5,6-tetrafluoro-tricyclo[6.2.2.0^2,7]dodeca-2⁽⁷⁾,3,5,9-tetraene(128816-99-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 128816-99-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 128816-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,8,1 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 128816-99:
(8*1)+(7*2)+(6*8)+(5*8)+(4*1)+(3*6)+(2*9)+(1*9)=159
159 % 10 = 9
So 128816-99-9 is a valid CAS Registry Number.

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128816-99-9Relevant academic research and scientific papers

TETRAFLUOROBENZOBARRELENE AND ITS DERIVATIVES IN REACTIONS WITH SULFENYL HALIDES

Nisnevich, G. A.,Mamatyuk, V. I.,Barkhash, V. A.,Velikokhat'ko, T. N.,Sadovaya, N. K.,et al.

, p. 70 - 85 (2007/10/02)

The reaction of tetrafluorobenzobarrelene and its derivatives with sulfenyl halides (RSY) in acetic acid, nitromethane, and methylene chloride leads to the formation of trans-β-halogeno sulfides.The use of the acetic acid-lithium perchlorate, formic acid,

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