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CAS

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82105-09-7

Thiophenyl-α-phenylcinnamat is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 82105-09-7 Structure

  • Basic information

    1. Product Name: Thiophenyl-α-phenylcinnamat
    2. Synonyms:
    3. CAS NO:82105-09-7
    4. Molecular Formula:
    5. Molecular Weight: 316.423
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82105-09-7.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: Thiophenyl-α-phenylcinnamat(CAS DataBase Reference)
    10. NIST Chemistry Reference: Thiophenyl-α-phenylcinnamat(82105-09-7)
    11. EPA Substance Registry System: Thiophenyl-α-phenylcinnamat(82105-09-7)

  • 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: 82105-09-7(Hazardous Substances Data)

82105-09-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82105-09-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,0 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82105-09:
(7*8)+(6*2)+(5*1)+(4*0)+(3*5)+(2*0)+(1*9)=97
97 % 10 = 7
So 82105-09-7 is a valid CAS Registry Number.

82105-09-7Upstream product

82105-09-7Downstream Products

82105-09-7Relevant articles and documents

Catalytic enantioselective one-pot approach to cis- and trans-2,3-diaryl substituted 1,5-benzothiazepines

Meninno, Sara,Quaratesi, Ilaria,Volpe, Chiara,Mazzanti, Andrea,Lattanzi, Alessandra

, p. 6923 - 6934 (2018)

The first enantioselective catalytic approach to cis- and trans-2,3-diaryl substituted 1,5-benzothiazepines has been conveniently developed in a one-pot fashion, starting from α,β-unsaturated acyl pyrazoles and 2-aminothiophenol. The organocatalytic two-s

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