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1413920-10-1

1-phenyl-3-(p-tolyl)-1H-naphtho[1,2-e][1,3]oxazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1413920-10-1 Structure

  • Basic information

    1. Product Name: 1-phenyl-3-(p-tolyl)-1H-naphtho[1,2-e][1,3]oxazine
    2. Synonyms:
    3. CAS NO:1413920-10-1
    4. Molecular Formula:
    5. Molecular Weight: 349.432
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1413920-10-1.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: 1-phenyl-3-(p-tolyl)-1H-naphtho[1,2-e][1,3]oxazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-phenyl-3-(p-tolyl)-1H-naphtho[1,2-e][1,3]oxazine(1413920-10-1)
    11. EPA Substance Registry System: 1-phenyl-3-(p-tolyl)-1H-naphtho[1,2-e][1,3]oxazine(1413920-10-1)

  • 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: 1413920-10-1(Hazardous Substances Data)

1413920-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1413920-10-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,3,9,2 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1413920-10:
(9*1)+(8*4)+(7*1)+(6*3)+(5*9)+(4*2)+(3*0)+(2*1)+(1*0)=121
121 % 10 = 1
So 1413920-10-1 is a valid CAS Registry Number.

1413920-10-1Downstream Products

1413920-10-1Relevant articles and documents

An Inverse Electron Demand Azo-Diels-Alder Reaction of o -Quinone Methides and Imino Ethers: Synthesis of Benzocondensed 1,3-Oxazines

Osipov, Dmitry V.,Osyanin, Vitaly A.,Khaysanova, Guzel D.,Masterova, Elvira R.,Krasnikov, Pavel E.,Klimochkin, Yuri N.

, p. 4775 - 4785 (2018)

We have studied the reactions of o-quinone methide precursors with imino ethers. The reaction provides a versatile route to substituted 1,3-benzoxazines. The proposed reaction mechanism involves the generation of the o-quinone methide intermediates, imino

Synthesis, antimicrobial and cytotoxicity study of 1,3-disubstituted-1H- naphtho[1,2-e][1,3]oxazines

Verma, Vikas,Singh, Kuldeep,Kumar, Devinder,Klap?tke, Thomas M.,Stierstorfer, J?rg,Narasimhan, Balasubramanian,Qazi, Asif Khurshid,Hamid, Abid,Jaglan, Sundeep

, p. 195 - 202 (2013/01/15)

A series of new 1,3-disubstituted-1H-naphtho[1,2-e][1,3]oxazines (3 and 7) was synthesized in good yields and the structure was determined with the help of NMR, 2D-NMR, HRMS studies and X-ray crystallography. These compounds were tested in vitro for their

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