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1415662-61-1

N-(1,3-benzothiazol-2-yl)-3-(4-ethoxyphenyl)acrylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1415662-61-1 Structure

  • Basic information

    1. Product Name: N-(1,3-benzothiazol-2-yl)-3-(4-ethoxyphenyl)acrylamide
    2. Synonyms: N-(1,3-benzothiazol-2-yl)-3-(4-ethoxyphenyl)acrylamide
    3. CAS NO:1415662-61-1
    4. Molecular Formula: C18H16N2O2S
    5. Molecular Weight: 324.39684
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1415662-61-1.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: N-(1,3-benzothiazol-2-yl)-3-(4-ethoxyphenyl)acrylamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(1,3-benzothiazol-2-yl)-3-(4-ethoxyphenyl)acrylamide(1415662-61-1)
    11. EPA Substance Registry System: N-(1,3-benzothiazol-2-yl)-3-(4-ethoxyphenyl)acrylamide(1415662-61-1)

  • 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: 1415662-61-1(Hazardous Substances Data)

1415662-61-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415662-61-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,6,6 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1415662-61:
(9*1)+(8*4)+(7*1)+(6*5)+(5*6)+(4*6)+(3*2)+(2*6)+(1*1)=151
151 % 10 = 1
So 1415662-61-1 is a valid CAS Registry Number.

1415662-61-1Downstream Products

1415662-61-1Relevant articles and documents

Synthesis of novel cinnamoyl amides using a solvent-free microwave-assisted method

Pellon, Rolando F.,Docampo, Maite L.

, p. 537 - 552 (2013/01/15)

A novel series of potential biologically active new cinnamoyl amides were synthesized in good yield and short reaction times. We have studied the one-pot, solvent-free reaction of cinnamic acid derivatives with aromatic amines using 1,3-dicyclohexylcarbodiimide under microwave irradiation in the presence of small quantities of dimethylformamide to improve energy transfer.

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