Cas 133707-99-0,Benzylsulfanyl-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octylsulfanyl)-acetic acid ethyl ester

133707-99-0

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Basic information

Product Name: Benzylsulfanyl-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octylsulfanyl)-acetic acid ethyl ester
Synonyms:
CAS NO:133707-99-0
Molecular Formula:
Molecular Weight: 588.454
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: Benzylsulfanyl-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octylsulfanyl)-acetic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzylsulfanyl-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octylsulfanyl)-acetic acid ethyl ester(133707-99-0)
EPA Substance Registry System: Benzylsulfanyl-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octylsulfanyl)-acetic acid ethyl ester(133707-99-0)

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: 133707-99-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 133707-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,7,0 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 133707-99:
(8*1)+(7*3)+(6*3)+(5*7)+(4*0)+(3*7)+(2*9)+(1*9)=130
130 % 10 = 0
So 133707-99-0 is a valid CAS Registry Number.

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133707-99-0Relevant academic research and scientific papers

SYNTHESE D'α-CHLORO (2-F-ALKYL ETHYL THIO) ACETATES D'ETHYLE EN VUE DE L'OBTENTION DE PRECURSEURS DE TENSIO-ACTIFS BICAUDAUX F-ALKYLES

Dieng, S. Y.,Roman, L.,Szoenyi, F.,Cambon, A.

, p. 155 - 164 (2007/10/02)

In this work we report the synthesis of ethyl α-chloro(2-F-alkylethylthio)acetates (F-alkyl: C4F9-, C6F13-, C8F17-) which are potential synthetic intermediates.We investigated their reactivity with mercaptans and alcohols: the dithioacetal compounds are e

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