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56963-63-4

ethyl 3-(4-chlorophenylamino)crotonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 56963-63-4 Structure

  • Basic information

    1. Product Name: ethyl 3-(4-chlorophenylamino)crotonate
    2. Synonyms: ethyl 3-(4-chlorophenylamino)crotonate
    3. CAS NO:56963-63-4
    4. Molecular Formula:
    5. Molecular Weight: 239.702
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 56963-63-4.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: ethyl 3-(4-chlorophenylamino)crotonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 3-(4-chlorophenylamino)crotonate(56963-63-4)
    11. EPA Substance Registry System: ethyl 3-(4-chlorophenylamino)crotonate(56963-63-4)

  • 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: 56963-63-4(Hazardous Substances Data)

56963-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56963-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,6 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56963-63:
(7*5)+(6*6)+(5*9)+(4*6)+(3*3)+(2*6)+(1*3)=164
164 % 10 = 4
So 56963-63-4 is a valid CAS Registry Number.

56963-63-4Relevant articles and documents

Synthesis, antimicrobial activities and cytogenetic studies of newer diazepino quinoline derivatives via Vilsmeier-Haack reaction

Nandhakumar,Suresh,Jude, A.L. Calistus,Rajesh kannan,Mohan

, p. 1128 - 1136 (2007)

The study of the Vilsmeier-Haack reagent on 4-hydroxyquinaldines resulted in a new versatile intermediate 4-chloro-3-formyl-2-(2-hydroxy-ethene-1-yl)quinolines, which on further treatment with hydrazine hydrate yielded the desired diazepino quinoline derivatives. All the synthesized diazepino quinoline derivatives are screened for their antibacterial and antifungal activities. Cytogenetic analysis of the samples is also reported.

Synthesis and biological screening of some new novel indole derivatives

Mehta,Sikotra,Shah

, p. 2594 - 2597 (2007/10/03)

Synthesis of some novel indole derivatives has been undertaken by the reaction of 1,4-benzoquinone with ethyl-β-(arylamino)-crotonates in the presence/absence of nitrogen atmosphere. The products 1a-o have been screened for their antimicrobial activity an

Vilsmeier-Haack reaction on quinaldines

Nandha Kumar,Suresh,Mohan

, p. 2069 - 2073 (2007/10/03)

The study of the Vilsmeier-Haack reaction on 4-hydroxyquinaldines resulted with the preparation of rarely existing 4-chloro-3-formyl-2(vinyl-1-ol)-quinolines.

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