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1609483-03-5

ethyl 5-(4-chlorophenyl)-1-(4-phenylthiazol-2-yl)-1H-pyrazole-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • ethyl 5-(4-chlorophenyl)-1-(4-phenylthiazol-2-yl)-1H-pyrazole-3-carboxylate

    Cas No: 1609483-03-5

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  • 1609483-03-5 Structure

  • Basic information

    1. Product Name: ethyl 5-(4-chlorophenyl)-1-(4-phenylthiazol-2-yl)-1H-pyrazole-3-carboxylate
    2. Synonyms:
    3. CAS NO:1609483-03-5
    4. Molecular Formula:
    5. Molecular Weight: 409.896
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1609483-03-5.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: ethyl 5-(4-chlorophenyl)-1-(4-phenylthiazol-2-yl)-1H-pyrazole-3-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 5-(4-chlorophenyl)-1-(4-phenylthiazol-2-yl)-1H-pyrazole-3-carboxylate(1609483-03-5)
    11. EPA Substance Registry System: ethyl 5-(4-chlorophenyl)-1-(4-phenylthiazol-2-yl)-1H-pyrazole-3-carboxylate(1609483-03-5)

  • 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: 1609483-03-5(Hazardous Substances Data)

1609483-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1609483-03-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,4,8 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1609483-03:
(9*1)+(8*6)+(7*0)+(6*9)+(5*4)+(4*8)+(3*3)+(2*0)+(1*3)=175
175 % 10 = 5
So 1609483-03-5 is a valid CAS Registry Number.

1609483-03-5Downstream Products

1609483-03-5Relevant articles and documents

An efficient one-pot synthesis of aryl-substituted 1-(thiazol-2-yl)-1H- pyrazole-3-carboxylates via a hantzsch synthesis-knorr reaction sequence

Gu, Chunhui,Zhai, Jiaojiao,Jiang, Jianan,Liu, Hongwei,Wang, Lei,Zhu, Dunru,Ji, Yafei

, p. 179 - 190 (2014/03/21)

The treatment of α-bromoalkyl aryl ketones and 2-(propan-2-ylidene) hydrazine carbothioamide afforded 4-aryl-2-(2-(propan-2-ylidene)hydrazinyl) thiazoles via a Hantzsch-thiazole synthesis, which reacted with 4-aryl-2,4-diketoesters via a sequential Knorr-

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