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1-Ethynyl-2,4-difluorobenzene, also known as CM, is an alkyne compound that features a fluoro group in the phenyl ring. This unique molecular structure endows it with specific properties that make it suitable for various applications in different industries.

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  • 302912-34-1 Structure
  • Basic information

    1. Product Name: 1-ETHYNYL-2.4-DIFLUOROBENZENE 97
    2. Synonyms: 1-ETHYNYL-2.4-DIFLUOROBENZENE 97;Benzene, 1-ethynyl-2,4-difluoro- (9CI);Benzene, 1-ethynyl-2,4-difluoro-;1-Ethynyl-2,4-difluorobenzene 97%
    3. CAS NO:302912-34-1
    4. Molecular Formula: C8H4F2
    5. Molecular Weight: 138.1141664
    6. EINECS: N/A
    7. Product Categories: HALIDE;Alkynyl;Halogenated Hydrocarbons;Organic Building Blocks
    8. Mol File: 302912-34-1.mol
  • Chemical Properties

    1. Melting Point: 29-32 °C(lit.)
    2. Boiling Point: 134.7°C at 760 mmHg
    3. Flash Point: 92 °F
    4. Appearance: /
    5. Density: 1.17g/cm3
    6. Vapor Pressure: 9.88mmHg at 25°C
    7. Refractive Index: 1.492
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-ETHYNYL-2.4-DIFLUOROBENZENE 97(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-ETHYNYL-2.4-DIFLUOROBENZENE 97(302912-34-1)
    12. EPA Substance Registry System: 1-ETHYNYL-2.4-DIFLUOROBENZENE 97(302912-34-1)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 10-36/37/38
    3. Safety Statements: 16-26-36
    4. RIDADR: UN 1325 4.1/PG 3
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: FLAMMABLE
    8. PackingGroup: III
    9. Hazardous Substances Data: 302912-34-1(Hazardous Substances Data)

302912-34-1 Usage

Uses

Used in Chemical Synthesis:
1-Ethynyl-2,4-difluorobenzene (CM) is used as a key intermediate in the synthesis of advanced materials for various applications. Its unique structure allows for the creation of novel compounds with enhanced properties.
Used in Polymer Industry:
1-Ethynyl-2,4-difluorobenzene (CM) is used as a monomer for the production of sulfonated poly(arylene ether)s containing CM and TFP [4-[Trifluorovinyl(oxy)]phenol]. These polymers exhibit improved properties, such as enhanced thermal stability and chemical resistance, making them suitable for various high-performance applications.
Used in Pharmaceutical Industry:
1-Ethynyl-2,4-difluorobenzene (CM) is used as a starting material for the preparation of 4-(2,4-difluorophenylethynyl)-3-methyl-5-phenylisoxazole, which has potential applications in the pharmaceutical industry. 1-ETHYNYL-2.4-DIFLUOROBENZENE 97 may exhibit biological activities that could be beneficial in the development of new drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 302912-34-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,2,9,1 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 302912-34:
(8*3)+(7*0)+(6*2)+(5*9)+(4*1)+(3*2)+(2*3)+(1*4)=101
101 % 10 = 1
So 302912-34-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H4F2/c1-2-6-3-4-7(9)5-8(6)10/h1,3-5H

302912-34-1 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (E1169)  1-Ethynyl-2,4-difluorobenzene  >96.0%(GC)

  • 302912-34-1

  • 1g

  • 890.00CNY

  • Detail
  • TCI America

  • (E1169)  1-Ethynyl-2,4-difluorobenzene  >96.0%(GC)

  • 302912-34-1

  • 5g

  • 3,450.00CNY

  • Detail
  • Aldrich

  • (556440)  1-Ethynyl-2,4-difluorobenzene  97%

  • 302912-34-1

  • 556440-5G

  • 1,806.48CNY

  • Detail

302912-34-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Ethynyl-2,4-difluorobenzene

1.2 Other means of identification

Product number -
Other names (2,4-difluorophenyl)acetylene

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:302912-34-1 SDS

302912-34-1Relevant articles and documents

Synthesis and Photochemical Application of Hydrofluoroolefin (HFO) Based Fluoroalkyl Building Block

Varga, Bálint,Tóth, Balázs L.,Béke, Ferenc,Csenki, János T.,Kotschy, András,Novák, Zoltán

, p. 4925 - 4929 (2021/07/01)

A novel fluoroalkyl iodide was synthesized on multigram scale from refrigerant gas HFO-1234yf as cheap industrial starting material in a simple, solvent-free, and easily scalable process. We demonstrated its applicability in a metal-free photocatalytic ATRA reaction to synthesize valuable fluoroalkylated vinyl iodides and proved the straightforward transformability of the products in cross-coupling chemistry to obtain conjugated systems.

Copper-Catalyzed Ring Opening of [1.1.1]Propellane with Alkynes: Synthesis of Exocyclic Allenic Cyclobutanes

Lasányi, Dániel,Tolnai, Gergely L.

supporting information, p. 10057 - 10062 (2019/12/24)

Despite the long history and interesting properties of propellanes, these compounds still have tremendous potential to be exploited in synthetic organic chemistry. Herein we disclose an experimentally simple procedure to achieve cyclobutane-containing allenes and alkynes through a copper-catalyzed ring opening of [1.1.1]propellane and subsequent reaction with ethynes.

Terminal alkynes from aldehydes via dehydrohalogenation of (Z)-1-iodo-1-alkenes with TBAF

Beshai, Mira,Dhudshia, Bhartesh,Mills, Ryan,Thadani, Avinash N.

supporting information; experimental part, p. 6794 - 6796 (2009/04/07)

Terminal alkynes were prepared in near quantitative yields via dehydrohalogenation of (Z)-1-iodo-1-alkenes with tetrabutylammonium fluoride (TBAF) under mild conditions. The methodology was expanded to include a one-pot, direct synthesis of terminal alkynes from aldehydes without the necessity of isolating and purifying the intermediate iodoalkene.

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