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111504-36-0

7-Bromo-3-phenyl-4-thioxo-3,5-diaza-tricyclo[5.2.2.01,5]undecane-2,6-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 111504-36-0 Structure

  • Basic information

    1. Product Name: 7-Bromo-3-phenyl-4-thioxo-3,5-diaza-tricyclo[5.2.2.01,5]undecane-2,6-dione
    2. Synonyms:
    3. CAS NO:111504-36-0
    4. Molecular Formula:
    5. Molecular Weight: 365.25
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 111504-36-0.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-Bromo-3-phenyl-4-thioxo-3,5-diaza-tricyclo[5.2.2.01,5]undecane-2,6-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-Bromo-3-phenyl-4-thioxo-3,5-diaza-tricyclo[5.2.2.01,5]undecane-2,6-dione(111504-36-0)
    11. EPA Substance Registry System: 7-Bromo-3-phenyl-4-thioxo-3,5-diaza-tricyclo[5.2.2.01,5]undecane-2,6-dione(111504-36-0)

  • 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: 111504-36-0(Hazardous Substances Data)

111504-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111504-36-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,5,0 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 111504-36:
(8*1)+(7*1)+(6*1)+(5*5)+(4*0)+(3*4)+(2*3)+(1*6)=70
70 % 10 = 0
So 111504-36-0 is a valid CAS Registry Number.

111504-36-0Downstream Products

111504-36-0Relevant articles and documents

Preparations of Perhydroimidazopyridine-3-thiones and Thiazole-5-spirocyclopropan-4(5H)-ones from Thioureas and α,γ-Dibromobutyryl Chloride under Phase-transfer Conditions

Okawara, Tadashi,Nakayama, Kentaro,Honda, Yoshihiro,Yamasaki, Tetsuo,Furukawa, Mitsuru

, p. 1733 - 1736 (2007/10/02)

The reaction of N-monosubstituted thioureas (1) with α,γ-dibromobutyryl chloride (2) was carried out in 5percent NaOH-CH2Cl2 to afford 2-alkyl(aryl)-6-bromo-2,3,7,8-tetrahydro-3-thioxo-6,8a-ethano-imidazopyridine-1,5(6H,8aH)-diones (3) and 2-alkyl(

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