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124570-60-1

5-piperidinopyrazolo[1,5-a]quinazoline-3-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124570-60-1 Structure

  • Basic information

    1. Product Name: 5-piperidinopyrazolo[1,5-a]quinazoline-3-carbonitrile
    2. Synonyms: 5-piperidinopyrazolo[1,5-a]quinazoline-3-carbonitrile;5-(piperidin-1-yl)pyrazolo[1,5-a]quinazoline-3-carbonitrile;Pyrazolo[1,5-a]quinazoline-3-carbonitrile, 5-(1-piperidinyl)-
    3. CAS NO:124570-60-1
    4. Molecular Formula: C16H15N5
    5. Molecular Weight: 277.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124570-60-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-piperidinopyrazolo[1,5-a]quinazoline-3-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-piperidinopyrazolo[1,5-a]quinazoline-3-carbonitrile(124570-60-1)
    11. EPA Substance Registry System: 5-piperidinopyrazolo[1,5-a]quinazoline-3-carbonitrile(124570-60-1)

  • 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: 124570-60-1(Hazardous Substances Data)

124570-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124570-60-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,5,7 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 124570-60:
(8*1)+(7*2)+(6*4)+(5*5)+(4*7)+(3*0)+(2*6)+(1*0)=111
111 % 10 = 1
So 124570-60-1 is a valid CAS Registry Number.

124570-60-1Downstream Products

124570-60-1Relevant articles and documents

An unexpected aminolysis in the synthesis of 5-substituted 3-(1H-tetrazol-5-yl)pyrazolo[1,5-a]quinazolines

Peet

, p. 713 - 716 (1989)

A synthetic route to 5-substituted 3-(1H-tetrazol-5-yl)pyrazolo[1,5-a]quinazolines is described. An unexpected displacement of a 4-morpholinyl group from the 5-position of this system occurred during tetrazole formation by the ammonia produced by in situ generation of hydrazoic acid from ammonium chloride and sodium azide.

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