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401-06-9

β,β-Dichloro-α-fluoro-3-trifluoromethyl-styrene is a synthetic organic compound characterized by its unique molecular structure. It is a halogenated derivative of styrene, with two chlorine atoms attached to the β-carbon (the carbon adjacent to the phenyl ring), a fluorine atom at the α-carbon (the carbon directly attached to the phenyl ring), and a trifluoromethyl group (-CF3) at the 3-position relative to the phenyl ring. β,β-dichloro-α-fluoro-3-trifluoromethyl-styrene is of interest in the field of organic chemistry, particularly for its potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its specific properties, such as reactivity and stability, make it a valuable intermediate in various chemical reactions. The compound's structure also contributes to its potential as a precursor in the development of new materials with unique physical and chemical properties.

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  • 401-06-9 Structure

  • Basic information

    1. Product Name: β,β-dichloro-α-fluoro-3-trifluoromethyl-styrene
    2. Synonyms: β,β-dichloro-α-fluoro-3-trifluoromethyl-styrene
    3. CAS NO:401-06-9
    4. Molecular Formula:
    5. Molecular Weight: 259.03
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 401-06-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: β,β-dichloro-α-fluoro-3-trifluoromethyl-styrene(CAS DataBase Reference)
    10. NIST Chemistry Reference: β,β-dichloro-α-fluoro-3-trifluoromethyl-styrene(401-06-9)
    11. EPA Substance Registry System: β,β-dichloro-α-fluoro-3-trifluoromethyl-styrene(401-06-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 401-06-9(Hazardous Substances Data)

401-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 401-06-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 401-06:
(5*4)+(4*0)+(3*1)+(2*0)+(1*6)=29
29 % 10 = 9
So 401-06-9 is a valid CAS Registry Number.

401-06-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name β,β-dichloro-α-fluoro-3-trifluoromethyl-styrene

1.2 Other means of identification

Product number -
Other names β,β-Dichlor-α-fluor-3-trifluormethyl-styrol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:401-06-9 SDS

401-06-9Relevant articles and documents

Preparation of Fluorine-Containing Phenylacetylenes by the Method of Introduction of the Ethynyl Group Using 1,1-Dichloro-2,2-difluroethene

Kodaira, Kazuo,Okuhara, Kunio

, p. 1625 - 1632 (2007/10/02)

Phenylacetylenes (ArCCH) having fluoro- or trifluoromethyl substituents (o-, m-, p-F; o-, m-, p-CF3; 2,4-, 2,5-, 2,6-, 3,5-(CF3)2) have been prepared from bromobenzenes (ArBr) and benzenes (ArH) using 1,1,-dichloro-2,2-difluoroethene (1) by a two-step route: ArLi or ArMgBr->ArCF=CCl2->ArCCLi.Upon careful treatment at -70 deg C with 1, o-fluorophenyllithium gave o-FC6H4CF=CCl2 in good yield, together with benzyne-derived products, such as o-(o-FC6H4)C6H4CF=CCl2.Lithiation of m-bis(trifluoromethyl)benzene at 0 deg C for 9 h (24 h) followed by treatment with bromine gave 1-bromo-2,4-, 2,6-, and 3,5-bis(trifluoromethyl)benzene in 35 (38), 31 (36), and 8percent (6percent) yield, respectively.

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