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(3-phenyl-2-thienyl)methanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 157664-15-8 Structure
  • Basic information

    1. Product Name: (3-phenyl-2-thienyl)methanamine
    2. Synonyms: (3-phenyl-2-thienyl)methanamine
    3. CAS NO:157664-15-8
    4. Molecular Formula: C11H11NS
    5. Molecular Weight: 189.27674
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 157664-15-8.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: (3-phenyl-2-thienyl)methanamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-phenyl-2-thienyl)methanamine(157664-15-8)
    11. EPA Substance Registry System: (3-phenyl-2-thienyl)methanamine(157664-15-8)
  • 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: 157664-15-8(Hazardous Substances Data)

157664-15-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157664-15-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,6,6 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 157664-15:
(8*1)+(7*5)+(6*7)+(5*6)+(4*6)+(3*4)+(2*1)+(1*5)=158
158 % 10 = 8
So 157664-15-8 is a valid CAS Registry Number.

157664-15-8Relevant articles and documents

An Efficient General Route to Furo-, Pyrido- and Thieno-benzazepines via Pd0 Catalysed Cross Coupling Reactions and Nitrile Ylide Cyclisations

Finch, Harry,Reece, Donald H.,Sharp, John T.

, p. 1193 - 1204 (2007/10/02)

The cyclisation of diene-conjugated nitrile ylides of the general type 1, in which the conjugated system consists of a benzene ring and a five- or a six-membered heterocyclic ring, provides an effective route to fully unsaturated heterocyclobenzazepines.The combination of this cyclisation with a direct route to the nitrile ylide precursors via Pd0 catalysed cross-coupling gives an efficient general synthetic route to these systems from readily available starting materials.

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