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1233127-10-0

5-(4-chlorophenyl)-2-phenyl-4-(thiophen-2-yl)furan-3-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1233127-10-0 Structure

  • Basic information

    1. Product Name: 5-(4-chlorophenyl)-2-phenyl-4-(thiophen-2-yl)furan-3-carbonitrile
    2. Synonyms: 5-(4-chlorophenyl)-2-phenyl-4-(thiophen-2-yl)furan-3-carbonitrile
    3. CAS NO:1233127-10-0
    4. Molecular Formula:
    5. Molecular Weight: 361.851
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1233127-10-0.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: 5-(4-chlorophenyl)-2-phenyl-4-(thiophen-2-yl)furan-3-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(4-chlorophenyl)-2-phenyl-4-(thiophen-2-yl)furan-3-carbonitrile(1233127-10-0)
    11. EPA Substance Registry System: 5-(4-chlorophenyl)-2-phenyl-4-(thiophen-2-yl)furan-3-carbonitrile(1233127-10-0)

  • 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: 1233127-10-0(Hazardous Substances Data)

1233127-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1233127-10-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,3,1,2 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1233127-10:
(9*1)+(8*2)+(7*3)+(6*3)+(5*1)+(4*2)+(3*7)+(2*1)+(1*0)=100
100 % 10 = 0
So 1233127-10-0 is a valid CAS Registry Number.

1233127-10-0Downstream Products

1233127-10-0Relevant articles and documents

Synthesis of Functionalized Furans via Chemoselective Reduction/Wittig Reaction Using Catalytic Triethylamine and Phosphine

Lee, Chia-Jui,Chang, Tzu-Hsiu,Yu, Jhen-Kuei,Madhusudhan Reddy, Ganapuram,Hsiao, Ming-Yu,Lin, Wenwei

, p. 3758 - 3761 (2016)

An efficient protocol for the synthesis of highly functionalized furans via intramolecular Wittig reaction has been developed using catalytic amounts of phosphine and triethylamine. Silyl chloride served as the initial promoter to activate the phosphine oxide. Reduction of the activated phosphine oxide by hydrosilane resulted in generation of phosphine, while decomposition of Et3N·HCl resulted in regeneration of base, which mediated formation of phosphorus ylide. Remarkably, the in situ generated byproduct, Et3N·HCl, also catalyzes reduction of phosphine oxide.

Preparation of tetrasubstituted furans via intramolecular wittig reactions with phosphorus ylides as intermediates

Kao, Tzu-Ting,Syu, Siang-En,Jhang, Yi-Wun,Lin, Wenwei

supporting information; experimental part, p. 3066 - 3069 (2010/08/19)

Novel preparation of tetrasubstituted furans, starting from the Michael acceptors, tributylphosphine, and acyl chlorides, is realized. A broad range of highly functional furans can be efficiently generated in one step at room temperature within 10 min to 21 h in moderate to high yields (60-99%). The reaction was proposed to proceed via intramolecular Wittig-type reactions, using phosphorus ylides as intermediates.

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