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99967-80-3

4-Amino-2-phenyl-5-thiazolcarbonsaeure-methylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 99967-80-3 Structure

  • Basic information

    1. Product Name: 4-Amino-2-phenyl-5-thiazolcarbonsaeure-methylester
    2. Synonyms: 4-Amino-2-phenyl-5-thiazolcarbonsaeure-methylester
    3. CAS NO:99967-80-3
    4. Molecular Formula:
    5. Molecular Weight: 234.279
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 99967-80-3.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-Amino-2-phenyl-5-thiazolcarbonsaeure-methylester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Amino-2-phenyl-5-thiazolcarbonsaeure-methylester(99967-80-3)
    11. EPA Substance Registry System: 4-Amino-2-phenyl-5-thiazolcarbonsaeure-methylester(99967-80-3)

  • 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: 99967-80-3(Hazardous Substances Data)

99967-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99967-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,9,6 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 99967-80:
(7*9)+(6*9)+(5*9)+(4*6)+(3*7)+(2*8)+(1*0)=223
223 % 10 = 3
So 99967-80-3 is a valid CAS Registry Number.

99967-80-3Relevant articles and documents

Thiazoles from N-Cyanoimidates or 3-Cyanoisoureas and Thioglycolic Acid Derivatives

Ried, Walter,Kuhnt, Dietmar

, p. 780 - 784 (2007/10/02)

Novel thiazoles 3a-g, 4a-d are synthesized from N-cyanoimidates and 3-cyanoisoureas of type 1a-m and thioglycolic acid methyl ester (2a) as well as the amide (2b).The limitations of the reaction are outlined.The products are further converted into thiazolopyrimidines 6a-d and thiazolo-1,2,3-triazinones 7a-c.

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