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  • 1208333-40-7 Structure
  • Basic information

    1. Product Name: C12H19NO
    2. Synonyms: C12H19NO
    3. CAS NO:1208333-40-7
    4. Molecular Formula:
    5. Molecular Weight: 193.289
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1208333-40-7.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: C12H19NO(CAS DataBase Reference)
    10. NIST Chemistry Reference: C12H19NO(1208333-40-7)
    11. EPA Substance Registry System: C12H19NO(1208333-40-7)
  • 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: 1208333-40-7(Hazardous Substances Data)

1208333-40-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1208333-40-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,8,3,3 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1208333-40:
(9*1)+(8*2)+(7*0)+(6*8)+(5*3)+(4*3)+(3*3)+(2*4)+(1*0)=117
117 % 10 = 7
So 1208333-40-7 is a valid CAS Registry Number.

1208333-40-7Relevant articles and documents

A novel construction of 2-benzazepine scaffold based on TiCl 4-mediated tandem Mannich reaction - Aromatic electrophilic substitution

Li, Liangxi,Li, Zhiming,Wang, Quanrui

experimental part, p. 2754 - 2761 (2010/04/02)

A novel construction of 2-benzazepine derivatives based on TiCl 4-mediated tandem Mannich reaction of electron-rich benzyl iminium ions with alkenyl ethers and Friedel - Crafts-type alkylation is described. The protocol is amenable to provide the tricyclic furo[3,2-d][2]benzazepine and pyrano[3,2-d][2]benzazepine derivatives, respectively, with 2,3-dihydrofuran or 3,4-dihydro-2H-pyran as the substrates.

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