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CAS

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193345-67-4

Thiazolo[5,4-d]isoxazol-6(5H)-amine, 5-[(1,1-dimethylethyl)imino]-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 193345-67-4 Structure

  • Basic information

    1. Product Name: Thiazolo[5,4-d]isoxazol-6(5H)-amine, 5-[(1,1-dimethylethyl)imino]-3-phenyl-
    2. Synonyms:
    3. CAS NO:193345-67-4
    4. Molecular Formula: C14H16N4OS
    5. Molecular Weight: 288.373
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 193345-67-4.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: Thiazolo[5,4-d]isoxazol-6(5H)-amine, 5-[(1,1-dimethylethyl)imino]-3-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Thiazolo[5,4-d]isoxazol-6(5H)-amine, 5-[(1,1-dimethylethyl)imino]-3-phenyl-(193345-67-4)
    11. EPA Substance Registry System: Thiazolo[5,4-d]isoxazol-6(5H)-amine, 5-[(1,1-dimethylethyl)imino]-3-phenyl-(193345-67-4)

  • 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: 193345-67-4(Hazardous Substances Data)

193345-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193345-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,3,4 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 193345-67:
(8*1)+(7*9)+(6*3)+(5*3)+(4*4)+(3*5)+(2*6)+(1*7)=154
154 % 10 = 4
So 193345-67-4 is a valid CAS Registry Number.

193345-67-4Downstream Products

193345-67-4Relevant articles and documents

On the synthesis of fused thiazolo[5,4-d]isoxazoles and a novel rearrangement involving conversion of 5(4H)-isoxazolones to 4(5H)-isoxazolones

Chande,Joshi

, p. 403 - 409 (2007/10/03)

The interaction of 4-bromo-3-substituted-(4H)-isoxazol-5-ones (1) with alkyl/aryl thiocarbamides (2), 4-alkyl/aryl thiosemicarbazides (7) and 2, 4-disubstituted thiosemicarbazides (12) afford 5-alkyl/ arylamino-3-substituted-thiazolo [5, 4-d]isoxazoles (3) and 6-amino/anilino-5-alkyl/arylimino-3-substituted-thiazolo[5, 4-d]isoxazoles respectively. An alternate unambiguous one step synthesis is described. The compounds have been characterised by chemical reactions and spectral data.

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