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144987-02-0

<15N>phenylacetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144987-02-0 Structure

  • Basic information

    1. Product Name: <15N>phenylacetonitrile
    2. Synonyms: <15N>phenylacetonitrile
    3. CAS NO:144987-02-0
    4. Molecular Formula:
    5. Molecular Weight: 118.144
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144987-02-0.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: <15N>phenylacetonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: <15N>phenylacetonitrile(144987-02-0)
    11. EPA Substance Registry System: <15N>phenylacetonitrile(144987-02-0)

  • 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: 144987-02-0(Hazardous Substances Data)

144987-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144987-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,9,8 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 144987-02:
(8*1)+(7*4)+(6*4)+(5*9)+(4*8)+(3*7)+(2*0)+(1*2)=160
160 % 10 = 0
So 144987-02-0 is a valid CAS Registry Number.

144987-02-0Downstream Products

144987-02-0Relevant articles and documents

A new route to functionalized 3-aminopyridazines by ANRORC type ring transformation of 1,2,4-triazines with carbon nucleophiles [1]

Rykowski,Wolinska,Van Der Plas

, p. 879 - 883 (2000)

The reaction of 3-chloro-6-phenyl-1,2,4-triazine 1a with carbon nucleophiles 2a-d bearing a cyano substituent at a carbanionic center has been studied. In all reactions the formation of the corresponding 3-aminopyridazines 3a-d takes place via ANRORC mech

METAL COMPLEX, AND METHOD FOR SYNTHESIS OF NITROGEN-CONTAINING ORGANIC COMPOUND USING METAL COMPLEX

-

Paragraph 0098-0099, (2017/04/29)

PROBLEM TO BE SOLVED: To provide a method that synthesizes a nitrogen-containing organic compound under a relatively mild condition and in a relatively simple process. SOLUTION: A method that synthesizes a nitrile compound includes a step for the reaction between an acid chloride and a complex represented by formula (1A) or formula (1B) (M1-M7 independently represent Ti, Zr, Hf, V, or the like; L1-L7 independently represent a ligand comprising a substituted/unsubstituted cyclopentadienyl derivative, a diphenylamine ligand or the like). SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

Synthesis of 13C, 15N-Enriched α-Dicarbonyl Model Adducts to Determine the Utility of 13Cand 15N NMR for Studying Mechanism-Based Inactivation of Cytochromes P-450 by Substituted Dichloroacetamides

Weiner, Scott J.,Holl, Susan M.,Covey, Douglas F.

, p. 122 - 127 (2007/10/02)

To determine the feasibility of using NMR to study the inactivation of cytochromes P-450 by dichloroacetamide-containing mechanism-based inactivators, 13C,15N-enriched compounds were synthesized, modeling adducts between the nucleophilic side-chain of cys

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