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5-CHLORO-3-(4-FLUOROPHENYL)-1-METHYL-1H-PYRAZOLE-4-CARBOXALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 857640-20-1 Structure
  • Basic information

    1. Product Name: 5-CHLORO-3-(4-FLUOROPHENYL)-1-METHYL-1H-PYRAZOLE-4-CARBOXALDEHYDE
    2. Synonyms: 5-CHLORO-3-(4-FLUOROPHENYL)-1-METHYL-1H-PYRAZOLE-4-CARBOXALDEHYDE
    3. CAS NO:857640-20-1
    4. Molecular Formula: C11H8ClFN2O
    5. Molecular Weight: 238.65
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 857640-20-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 369.4±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.34±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -1.76±0.10(Predicted)
    10. CAS DataBase Reference: 5-CHLORO-3-(4-FLUOROPHENYL)-1-METHYL-1H-PYRAZOLE-4-CARBOXALDEHYDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-CHLORO-3-(4-FLUOROPHENYL)-1-METHYL-1H-PYRAZOLE-4-CARBOXALDEHYDE(857640-20-1)
    12. EPA Substance Registry System: 5-CHLORO-3-(4-FLUOROPHENYL)-1-METHYL-1H-PYRAZOLE-4-CARBOXALDEHYDE(857640-20-1)
  • 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: 857640-20-1(Hazardous Substances Data)

857640-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 857640-20-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,6,4 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 857640-20:
(8*8)+(7*5)+(6*7)+(5*6)+(4*4)+(3*0)+(2*2)+(1*0)=191
191 % 10 = 1
So 857640-20-1 is a valid CAS Registry Number.

857640-20-1Downstream Products

857640-20-1Relevant articles and documents

Synthesis of poly-functionalized pyrazoles under Vilsmeier-Haack reaction conditions

Popov, Aleksandr V.,Kobelevskaya, Valentina A.,Larina, Ludmila I.,Rozentsveig, Igor B.

, p. 1 - 14 (2019/11/11)

Synthesis of 1,3-disubstituted 5-chloro-1H-pyrazole-4-carbaldehydes was achieved by formylation of the corresponding 5-chloro-1H-pyrazoles under Vilsmeier-Haack conditions.

PYRAZOLE DERIVATIVES AND USE THEREOF AS OREXIN RECEPTOR ANTAGONISTS

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Page/Page column 45; 47, (2008/06/13)

The present invention relates to the orexin receptor antagonists compounds of the general formula (I) as well as to their isomers, salts and solvates, to the pharmaceutical compositions containing them and to the therapeutic application thereof.

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