Cas 379-01-1,Benzene, (2,2-dichloro-1,1,2-trifluoroethyl)-

379-01-1

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Basic information

Product Name: Benzene, (2,2-dichloro-1,1,2-trifluoroethyl)-
Synonyms: 1-phenyl-2,2-dichloro-1,1,2-trifluoroethane;(2,2-dichloro-1,1,2-trifluoro-ethyl)-benzene;Benzene,(2,2-dichloro-1,1,2-trifluoroethyl);(2,2-Dichlor-1,1,2-trifluor-aethyl)-benzol;
CAS NO:379-01-1
Molecular Formula: C8H5Cl2F3
Molecular Weight: 229.02700
EINECS: N/A
Product Categories: N/A
Mol File: 379-01-1.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 197.3±40.0 °C(Predicted)
Flash Point: N/A
Appearance: N/A
Density: 1.411±0.06 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Benzene, (2,2-dichloro-1,1,2-trifluoroethyl)-(CAS DataBase Reference)
NIST Chemistry Reference: Benzene, (2,2-dichloro-1,1,2-trifluoroethyl)-(379-01-1)
EPA Substance Registry System: Benzene, (2,2-dichloro-1,1,2-trifluoroethyl)-(379-01-1)

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: 379-01-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 379-01-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 379-01:
(5*3)+(4*7)+(3*9)+(2*0)+(1*1)=71
71 % 10 = 1
So 379-01-1 is a valid CAS Registry Number.

379-01-1Upstream product

379-01-1Downstream Products

379-01-1Relevant academic research and scientific papers

Perhaloethyl aromatic compounds and perhaloethenyl aromatic compounds therefrom

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Example 1-2, (2008/06/13)

A synthesis is provided for α,β-difluoro-β-halo-ethenyl aromatic compounds such as α,β,β-trifluorostyrenes by a process of reacting CFX2CFXI, wherein each X is independently F or Cl, provided that at least one X is Cl and at least one X is F, with an aromatic compound Ar to form (CFX2CFX)n—Ar, wherein n is 1, 2 or 3, and subsequently dechlorohalogenating this product to form (CFX═CF)n—Ar. Novel synthetic intermediate compounds are provided.

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