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1001862-74-3

4-(4-CHLORO-PYRAZOL-1-YLMETHYL)-PHENYLAMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1001862-74-3 Structure

  • Basic information

    1. Product Name: 4-(4-CHLORO-PYRAZOL-1-YLMETHYL)-PHENYLAMINE
    2. Synonyms: ART-CHEM-BB B024948;4-(4-CHLORO-PYRAZOL-1-YLMETHYL)-PHENYLAMINE;AKOS B024948
    3. CAS NO:1001862-74-3
    4. Molecular Formula: C10H10ClN3
    5. Molecular Weight: 207.66
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1001862-74-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 395.9±27.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.31±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 4.46±0.10(Predicted)
    10. CAS DataBase Reference: 4-(4-CHLORO-PYRAZOL-1-YLMETHYL)-PHENYLAMINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-(4-CHLORO-PYRAZOL-1-YLMETHYL)-PHENYLAMINE(1001862-74-3)
    12. EPA Substance Registry System: 4-(4-CHLORO-PYRAZOL-1-YLMETHYL)-PHENYLAMINE(1001862-74-3)

  • 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: 1001862-74-3(Hazardous Substances Data)

1001862-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1001862-74-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,1,8,6 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1001862-74:
(9*1)+(8*0)+(7*0)+(6*1)+(5*8)+(4*6)+(3*2)+(2*7)+(1*4)=103
103 % 10 = 3
So 1001862-74-3 is a valid CAS Registry Number.

1001862-74-3Downstream Products

1001862-74-3Relevant articles and documents

Rapid Synthesis of Aryl Fluorides in Continuous Flow through the Balz–Schiemann Reaction

Park, Nathaniel H.,Senter, Timothy J.,Buchwald, Stephen L.

supporting information, p. 11907 - 11911 (2016/11/17)

The Balz–Schiemann reaction remains a highly utilized means for preparing aryl fluorides from anilines. However, the limitations associated with handling aryl diazonium salts often hinder both the substrate scope and scalability of this reaction. To address this, a new continuous flow protocol was developed that eliminates the need to isolate the aryl diazonium salts. The new process has enabled the fluorination of an array of aryl and heteroaryl amines.

HETEROARYL INHIBITORS OF PDE4

-

Paragraph 0822, (2014/05/24)

The present invention relates to compounds and methods useful as inhibitors of phosphodiesterase 4 (PDE4) for the treatment or prevention of disease.

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