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Furan, 3-fluoro-2-phenyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 562812-34-4 Structure
  • Basic information

    1. Product Name: Furan, 3-fluoro-2-phenyl- (9CI)
    2. Synonyms: Furan, 3-fluoro-2-phenyl- (9CI)
    3. CAS NO:562812-34-4
    4. Molecular Formula: C10H7FO
    5. Molecular Weight: 162.1603832
    6. EINECS: N/A
    7. Product Categories: HALIDE
    8. Mol File: 562812-34-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Furan, 3-fluoro-2-phenyl- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Furan, 3-fluoro-2-phenyl- (9CI)(562812-34-4)
    11. EPA Substance Registry System: Furan, 3-fluoro-2-phenyl- (9CI)(562812-34-4)
  • 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: 562812-34-4(Hazardous Substances Data)

562812-34-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 562812-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,2,8,1 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 562812-34:
(8*5)+(7*6)+(6*2)+(5*8)+(4*1)+(3*2)+(2*3)+(1*4)=154
154 % 10 = 4
So 562812-34-4 is a valid CAS Registry Number.

562812-34-4Downstream Products

562812-34-4Relevant articles and documents

Au-catalyzed intramolecular hydroalkoxylation of gem-difluorinated alkynols

Hamel, Jean-Denys,Paquin, Jean-Fran?ois

, p. 11 - 23 (2018/10/20)

The intramolecular hydroalkoxylation of gem-difluorinated alkynols was found possible under Au catalysis, allowing for the preparation of a series of fluorinated heterocycles. The nature of the solvent was found to be especially critical in the cyclizatio

Selective synthesis of fluorinated furan derivatives via AgNO 3-catalyzed activation of an electronically deficient triple bond

Arimitsu, Satoru,Hammond, Gerald B.

, p. 8559 - 8561 (2008/02/12)

(Chemical Equation Presented) The transition metal-catalyzed direct activation of electron deficient triple bonds was investigated by using the combined electron withdrawing effects of two fluorine atoms to modulate the electronic density of the triple bo

A novel approach of cycloaddition of difluorocarbene to α-β-unsaturated aldehydes and ketones: Synthesis of gem-difluorocyclopropyl ketones and 2-fluorofurans

Xu, Wei,Chen, Qing-Yun

, p. 1151 - 1156 (2007/10/03)

A series of gem-difluorocyclopropyl acetals and ketals are easily obtained in moderate yields from the [1 + 2] cycloaddition of difluorocarbene to 1,3-dioxolanes of α,β-unsaturated aromatic aldehydes and ketones. Hydrolysis of these fluorinated compounds under acidic conditions either gives the corresponding gem-difluorocyclopropyl ketones or 1-aryl-2-fluorofuran derivatives through intramolecular carbonium rearrangement with simultaneous ring cleavage.

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