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1025351-09-0

C16H12N2O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1025351-09-0 Structure

  • Basic information

    1. Product Name: C16H12N2O2
    2. Synonyms: C16H12N2O2
    3. CAS NO:1025351-09-0
    4. Molecular Formula:
    5. Molecular Weight: 264.283
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1025351-09-0.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: C16H12N2O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H12N2O2(1025351-09-0)
    11. EPA Substance Registry System: C16H12N2O2(1025351-09-0)

  • 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: 1025351-09-0(Hazardous Substances Data)

1025351-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1025351-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,3,5 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1025351-09:
(9*1)+(8*0)+(7*2)+(6*5)+(5*3)+(4*5)+(3*1)+(2*0)+(1*9)=100
100 % 10 = 0
So 1025351-09-0 is a valid CAS Registry Number.

1025351-09-0Downstream Products

1025351-09-0Relevant articles and documents

Synthesis of benzyl esters from the commercially available alcohols catalyzed by TBAI via C(sp3)-H bond functionalization

Dong, Dao-Qing,Zhang, Hui,Wang, Zu-Li

, p. 3780 - 3782 (2017/02/05)

A direct esterification of alcohols catalyzed by TBAI via C(sp3)-H bond functionalization was achieved under mild and clean conditions. A series of benzyl esters were obtained in good to excellent yields via the C(sp3)-H bond functionalization of alkyl-substituted azaarenes.

Bu4NI-catalyzed benzylic acyloxylation of alkylarenes with aromatic aldehydes

Huang, Juan,Li, Lan-Tao,Li, Hong-Ying,Husan, Ezizjan,Wang, Peng,Wang, Bin

supporting information, p. 10204 - 10206,3 (2020/08/24)

An nBu4NI-catalyzed benzylic C-H acyloxylation of alkylarenes with readily available aromatic aldehydes has been developed. These reactions occur under mild and clean reaction conditions using tert-butyl hydroperoxide as the green terminal oxid

Hydroxymethylations of aryl halides by Pd-catalyzed cross-couplings with (benzoyloxy)methylzinc iodide - Scope and limitations of the reaction

Hasník, Zbyněk,?ilhár, Peter,Hocek, Michal

, p. 543 - 546 (2008/12/22)

Palladium-catalyzed cross-coupling reactions of (benzoyloxymethyl)zinc iodide with diverse (het)aryl halides leading to (benzoyloxymethyl)(het)arenes were studied to define the scope of this reaction. It has been found that this reaction is only applicable for electron-deficient aryl halides and the most efficient it is for 2-halopyridines and 4-halopyrimidines. Deprotection of the intermediates gives (hydroxymethyl)pyridines and -pyrimidines in high yields. Georg Thieme Verlag Stuttgart.

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