Cas 1443455-84-2,(S)-1,1,1,3,3,3-hexafluoropropan-2-yl 3-(3-bromophenyl)-3-(phenylthio)propanoate

1443455-84-2

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Basic information

Product Name: (S)-1,1,1,3,3,3-hexafluoropropan-2-yl 3-(3-bromophenyl)-3-(phenylthio)propanoate
Synonyms: (S)-1,1,1,3,3,3-hexafluoropropan-2-yl 3-(3-bromophenyl)-3-(phenylthio)propanoate
CAS NO:1443455-84-2
Molecular Formula:
Molecular Weight: 487.26
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: (S)-1,1,1,3,3,3-hexafluoropropan-2-yl 3-(3-bromophenyl)-3-(phenylthio)propanoate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1,1,1,3,3,3-hexafluoropropan-2-yl 3-(3-bromophenyl)-3-(phenylthio)propanoate(1443455-84-2)
EPA Substance Registry System: (S)-1,1,1,3,3,3-hexafluoropropan-2-yl 3-(3-bromophenyl)-3-(phenylthio)propanoate(1443455-84-2)

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: 1443455-84-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1443455-84-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,3,4,5 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1443455-84:
(9*1)+(8*4)+(7*4)+(6*3)+(5*4)+(4*5)+(3*5)+(2*8)+(1*4)=162
162 % 10 = 2
So 1443455-84-2 is a valid CAS Registry Number.

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1443455-84-2Relevant academic research and scientific papers

Organocatalytic asymmetric sulfa-michael addition of thiols to α,β-unsaturated hexafluoroisopropyl esters: Expeditious access to (R)-thiazesim

Fang, Xin,Li, Jun,Wang, Chun-Jiang

, p. 3448 - 3451 (2013/07/26)

A highly efficient organocatalytic asymmetric SMA reaction of hexafluoroisopropyl α,β-unsaturated esters has been developed. Introducing electron-withdrawing hexafluoroisopropyl ester is crucial to enhancing the electrophilicity of unsaturated esters as S

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