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CAS

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93019-52-4

4-(toluene-4-sulfonyl)-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93019-52-4 Structure

  • Basic information

    1. Product Name: 4-(toluene-4-sulfonyl)-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine
    2. Synonyms: 4-(toluene-4-sulfonyl)-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine
    3. CAS NO:93019-52-4
    4. Molecular Formula:
    5. Molecular Weight: 302.397
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93019-52-4.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: 4-(toluene-4-sulfonyl)-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(toluene-4-sulfonyl)-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine(93019-52-4)
    11. EPA Substance Registry System: 4-(toluene-4-sulfonyl)-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine(93019-52-4)

  • 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: 93019-52-4(Hazardous Substances Data)

93019-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93019-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,0,1 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93019-52:
(7*9)+(6*3)+(5*0)+(4*1)+(3*9)+(2*5)+(1*2)=124
124 % 10 = 4
So 93019-52-4 is a valid CAS Registry Number.

93019-52-4Relevant articles and documents

Asymmetric synthesis of vabicaserin via oxidative multicomponent annulation and asymmetric hydrogenation of a 3,4-substituted quinolinium salt

Dragan, Vladimir,McWilliams, J. Christopher,Miller, Ross,Sutherland, Karen,Dillon, John L.,O'Brien, Michael K.

, p. 2942 - 2945 (2013)

An efficient, asymmetric synthesis of the 5-HT2C agonist vabicaserin in four chemical steps and 54% overall yield from commercially available benzodiazepine was achieved. The synthesis was highlighted by a novel oxidative, multicomponent reaction to affect the quinolinium ring assembly in one step followed by an unprecedented asymmetric hydrogenation of a 3,4-substituted quinolinium salt.

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