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CAS

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32407-75-3

1-(3,4-dimethoxyphenyl)-7,8-dimethoxy-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 32407-75-3 Structure

  • Basic information

    1. Product Name: 1-(3,4-dimethoxyphenyl)-7,8-dimethoxy-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine
    2. Synonyms: 1-(3,4-dimethoxyphenyl)-7,8-dimethoxy-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine
    3. CAS NO:32407-75-3
    4. Molecular Formula:
    5. Molecular Weight: 357.45
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 32407-75-3.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: 1-(3,4-dimethoxyphenyl)-7,8-dimethoxy-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(3,4-dimethoxyphenyl)-7,8-dimethoxy-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine(32407-75-3)
    11. EPA Substance Registry System: 1-(3,4-dimethoxyphenyl)-7,8-dimethoxy-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine(32407-75-3)

  • 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: 32407-75-3(Hazardous Substances Data)

32407-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32407-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,4,0 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32407-75:
(7*3)+(6*2)+(5*4)+(4*0)+(3*7)+(2*7)+(1*5)=93
93 % 10 = 3
So 32407-75-3 is a valid CAS Registry Number.

32407-75-3Downstream Products

32407-75-3Relevant articles and documents

Aryne-Mediated Arylation of the 3-Benzazepine Scaffold: One-Pot Synthesis of 1-Aryl-3-methyl-2,3,4,5-tetrahydro-1 H -3-benzazepines

Singh, Kamal Nain,Singh, Paramjit,Sharma, Esha,Kaur, Manjot,Deol, Yadwinder Singh

, p. 3212 - 3220 (2015)

The coupling of β-amino carbanions derived from 3-benzA"azeA"pines with in situ generated arynes has been demonstrated as a convenient route for the direct synthesis of a variety of 1-aryl-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepines, including the biologically active drug molecule SCH 12679.

Rearrangement of 1-(α-Hydroxybenzyl)-1,2,3,4-tetrahydroisoquinolines to 1-Phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines

McMahon, Robert M.,Thornber, Craig W.,Ruchirawat, Somsak

, p. 2163 - 2168 (2007/10/02)

When methoxy-substituted 1-(α-hydroxybenzyl)-1,2,3,4-tetrahydroisoquinolines are heated in formic acid they rearrange initially to give 5-phenyl-2,3-dihydro-1H-3-benzazepines which, on further heating in formic acid, are reduced to 1-phenyl-2,3,4,5-tetrah

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