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150869-53-7

N-(4-bromophenylmethyl)-N-propylamine-N-tritylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 150869-53-7 Structure

  • Basic information

    1. Product Name: N-(4-bromophenylmethyl)-N-propylamine-N-tritylamine
    2. Synonyms: N-(4-bromophenylmethyl)-N-propylamine-N-tritylamine
    3. CAS NO:150869-53-7
    4. Molecular Formula:
    5. Molecular Weight: 470.452
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 150869-53-7.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: N-(4-bromophenylmethyl)-N-propylamine-N-tritylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-bromophenylmethyl)-N-propylamine-N-tritylamine(150869-53-7)
    11. EPA Substance Registry System: N-(4-bromophenylmethyl)-N-propylamine-N-tritylamine(150869-53-7)

  • 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: 150869-53-7(Hazardous Substances Data)

150869-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150869-53-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,8,6 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 150869-53:
(8*1)+(7*5)+(6*0)+(5*8)+(4*6)+(3*9)+(2*5)+(1*3)=147
147 % 10 = 7
So 150869-53-7 is a valid CAS Registry Number.

150869-53-7Relevant articles and documents

An efficient synthesis of an angiotensin II antagonist (A-81988)

Kerdesky,Haight,Narayanan,Nordeen,Scarpetti,Seif,Wittenberger,Morton

, p. 2027 - 2039 (1993)

A new and efficient synthesis of A-81988, an angiotensin II antagonist, is described. The preparation utilizes a novel method for tetrazole formation from nitriles requiring trimethylsilyl azide and a catalytic amount of dialkyltin oxide.

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