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2-Butenedioic acid, 2-[(3,5-dimethylphenyl)amino]-, dimethyl ester, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92952-51-7 Structure
  • Basic information

    1. Product Name: 2-Butenedioic acid, 2-[(3,5-dimethylphenyl)amino]-, dimethyl ester, (Z)-
    2. Synonyms:
    3. CAS NO:92952-51-7
    4. Molecular Formula: C14H17NO4
    5. Molecular Weight: 263.293
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92952-51-7.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: 2-Butenedioic acid, 2-[(3,5-dimethylphenyl)amino]-, dimethyl ester, (Z)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Butenedioic acid, 2-[(3,5-dimethylphenyl)amino]-, dimethyl ester, (Z)-(92952-51-7)
    11. EPA Substance Registry System: 2-Butenedioic acid, 2-[(3,5-dimethylphenyl)amino]-, dimethyl ester, (Z)-(92952-51-7)
  • 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: 92952-51-7(Hazardous Substances Data)

92952-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92952-51-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,5 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92952-51:
(7*9)+(6*2)+(5*9)+(4*5)+(3*2)+(2*5)+(1*1)=157
157 % 10 = 7
So 92952-51-7 is a valid CAS Registry Number.

92952-51-7Relevant articles and documents

Introduction of a clean and promising protocol for the synthesis of β-amino-acrylates and 1,4-benzoheterocycles: An emerging innovation

Choudhary, Garima,Peddinti, Rama Krishna

experimental part, p. 3290 - 3299 (2011/12/16)

A highly efficient, elegant and simple procedure with exceptionally mild conditions has been proposed for the synthesis of β-amino-acrylate derivatives and an array of biologically and pharmaceutically active benzoheterocycles. The protocol offers a valua

Oxidation of Enamine-esters with Lead Tetra-acetate. Part 2. Products from N-Aryl- and N-Benzyl-aminofumarates.

Vernon, John M.,Carr, Richard M.,Sukari, Mohamed A.

, p. 1310 - 1334 (2007/10/02)

Dimethyl anilinofumarate and N-benzylaminofumarate are oxidised by lead tetra-acetate to pyrroline, pyrrolin-2-one and pyrrole derivatives.Some other N-arylaminofumarates give the corresponding oxanilates by autoxidative cleavage.

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