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156938-79-3

7-Benzyloxy-2-methylthio-4,5-dihydro-3H-benzazepin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

156938-79-3

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  • 156938-79-3 Structure

  • Basic information

    1. Product Name: 7-Benzyloxy-2-methylthio-4,5-dihydro-3H-benzazepin
    2. Synonyms:
    3. CAS NO:156938-79-3
    4. Molecular Formula:
    5. Molecular Weight: 297.421
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156938-79-3.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: 7-Benzyloxy-2-methylthio-4,5-dihydro-3H-benzazepin(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-Benzyloxy-2-methylthio-4,5-dihydro-3H-benzazepin(156938-79-3)
    11. EPA Substance Registry System: 7-Benzyloxy-2-methylthio-4,5-dihydro-3H-benzazepin(156938-79-3)

  • 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: 156938-79-3(Hazardous Substances Data)

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156938-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156938-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,9,3 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 156938-79:
(8*1)+(7*5)+(6*6)+(5*9)+(4*3)+(3*8)+(2*7)+(1*9)=183
183 % 10 = 3
So 156938-79-3 is a valid CAS Registry Number.

156938-79-3Downstream Products

156938-79-3Relevant articles and documents

Lipoxygenase Inhibitors, III: Synthesis of Tetrahydrobenzazepinone Phenylhydrazones

Buege, Axel,Locke, Christian,Koehler, Thomas,Nuhn, Peter

, p. 99 - 104 (1994)

Tetrahydro-2H-benzazepin-2-ones as starting substances are synthesized by Beckmann rearrangement or Schmidt reaction.The tetrahydrobenzazepinones are transformed into the thiones, thiolactim ethers and phenylhydrazones.The compounds are tested as inhibitors of soja lipoxygenase.

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