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6-Methyl-3-phenylthiazolo<4,5-d>pyridazine-2,7(6H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 136353-56-5 Structure
  • Basic information

    1. Product Name: 6-Methyl-3-phenylthiazolo<4,5-d>pyridazine-2,7(6H)-dione
    2. Synonyms: 6-Methyl-3-phenylthiazolo<4,5-d>pyridazine-2,7(6H)-dione
    3. CAS NO:136353-56-5
    4. Molecular Formula:
    5. Molecular Weight: 259.288
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 136353-56-5.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: 6-Methyl-3-phenylthiazolo<4,5-d>pyridazine-2,7(6H)-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Methyl-3-phenylthiazolo<4,5-d>pyridazine-2,7(6H)-dione(136353-56-5)
    11. EPA Substance Registry System: 6-Methyl-3-phenylthiazolo<4,5-d>pyridazine-2,7(6H)-dione(136353-56-5)
  • 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: 136353-56-5(Hazardous Substances Data)

136353-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136353-56-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,3,5 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136353-56:
(8*1)+(7*3)+(6*6)+(5*3)+(4*5)+(3*3)+(2*5)+(1*6)=125
125 % 10 = 5
So 136353-56-5 is a valid CAS Registry Number.

136353-56-5Downstream Products

136353-56-5Relevant articles and documents

A Novel Synthesis of 2-Arylaminothiazolopyridazinones

Yamasaki, Tetsuo,Kawaminami, Eiji,Uchimura, Fumi,Okawara, Tadashi,Furukawa, Mitsuru

, p. 859 - 865 (2007/10/02)

The reaction of 5(4)-amino-4(5)-chloropyridazin-3(2H)-ones 1 (9) with methyl dithiocarbamates 2 gave 2-arylaminothiazolopyridazinones 3 (10).Treatment of 5(4)-alkylamino-4(5)-chloropyridazin-3(2H)-ones 5 (12) with 2 afforded the corresponding 2-aryliminothiazolopyridazinones 6 (13).Cyclization of 1a with phenylisothiocyanate produced 2-amino- and 2-iminothiazolopyridazinones 3a and 16.

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