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CAS

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74375-44-3

o-ethylaminobenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74375-44-3 Structure

  • Basic information

    1. Product Name: o-ethylaminobenzamide
    2. Synonyms: o-ethylaminobenzamide
    3. CAS NO:74375-44-3
    4. Molecular Formula:
    5. Molecular Weight: 164.207
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74375-44-3.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: o-ethylaminobenzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: o-ethylaminobenzamide(74375-44-3)
    11. EPA Substance Registry System: o-ethylaminobenzamide(74375-44-3)

  • 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: 74375-44-3(Hazardous Substances Data)

74375-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74375-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,7 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74375-44:
(7*7)+(6*4)+(5*3)+(4*7)+(3*5)+(2*4)+(1*4)=143
143 % 10 = 3
So 74375-44-3 is a valid CAS Registry Number.

74375-44-3Relevant articles and documents

Alkylamino derivatives of 4-aminomethylpyridine as inhibitors of copper-containing amine oxidases

Bertini, Vincenzo,Buffoni, Franca,Ignesti, Giovanni,Picci, Nevio,Trombino, Sonia,Iemma, Francesca,Alfei, Silvana,Pocci, Marco,Lucchesini, Francesco,De Munno, Angela

, p. 664 - 670 (2007/10/03)

The first substratelike, reversible inhibitors of different copper amine oxidases (CAOs) with IC50 (M) as low as 2.0 × 10-8 corresponding to derivatives of 4-aminomethylpyridine with alkoxy (1a-d), alkylthio (2a,b), and alkylamino (3

A Versatile Synthesis of 3H-1(H),4(H)-Benzodiazepin-2,5-diones

Mohiuddin, G.,Reddy, P. S. N.,Ahmed, Khalil,Ratnam, C. V.

, p. 905 - 907 (2007/10/02)

Reaction of isatoic anhydrides (1) and α-amino acids (2) in glacial acetic acid under reflux gave 3H-1(H),4(H)-benzodiazepin-2,5-diones (3) in good yields.These compounds have been characterised by UV, IR, mass, PMR and 13C-NMR spectra.

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