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10353-44-3

3-BENZYL-2H-1,3-BENZOTHIAZINE-2,4(3H)-DIONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10353-44-3 Structure

  • Basic information

    1. Product Name: 3-BENZYL-2H-1,3-BENZOTHIAZINE-2,4(3H)-DIONE
    2. Synonyms: 3-BENZYL-2H-1,3-BENZOTHIAZINE-2,4(3H)-DIONE;3-benzyl-3,4-dihydro-2H-1,3-benzothiazine-2,4-dione
    3. CAS NO:10353-44-3
    4. Molecular Formula: C15H11NO2S
    5. Molecular Weight: 269.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10353-44-3.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: 3-BENZYL-2H-1,3-BENZOTHIAZINE-2,4(3H)-DIONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-BENZYL-2H-1,3-BENZOTHIAZINE-2,4(3H)-DIONE(10353-44-3)
    11. EPA Substance Registry System: 3-BENZYL-2H-1,3-BENZOTHIAZINE-2,4(3H)-DIONE(10353-44-3)

  • 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: 10353-44-3(Hazardous Substances Data)

10353-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10353-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,5 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10353-44:
(7*1)+(6*0)+(5*3)+(4*5)+(3*3)+(2*4)+(1*4)=63
63 % 10 = 3
So 10353-44-3 is a valid CAS Registry Number.

10353-44-3Downstream Products

10353-44-3Relevant articles and documents

N-alkylation of imides using phase transfer catalysts under solvent-free conditions

Jaskowska, Jolanta,Kowalski, Piotr

, p. 1371 - 1375 (2008)

(Chemical Equation Presented) N-Alkylation of imides in the reaction of imides and alkylhalides, catalyzed by PT catalysts under solvent-free conditions, has been developed. The reaction occurs in the presence of K 2CO3, and in many cases it takes place spontaneously. In the N-benzylation reaction, it has been recognized that TBAB (tetrabutylammonium bromide) and TBATFB (tetrabutylammonium tetrafluoroborate) show highest catalytic effect. Versatility and synthetic capacity of the solvent-free alkylation has been confirmed by N-benzylation and N-ethylation of various imides. The developed procedure gives easy access to N-(ω-bromoalkyl) imides.

A simple one-pot synthesis of benzoxazine-2,4-diones and benzothiazine-2,4-diones

Zhu, Xiaoxiang,Yu, Qian-sheng,Greig, Nigel H.,Flippen-Anderson, Judith L.,Brossi, Arnold

, p. 115 - 128 (2007/10/03)

A simple and efficient procedure has been developed for a one-pot synthesis of substituted benzoxazine-2,4-diones and benzothiazine-2,4-diones directly from salicylic acid (or thiosalicylic acid) and amines.

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