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1146596-37-3

N-[(5-amino-4-cyano-3-phenyl-2,3-dihydrothiophen-2-yl)carbonyl]morpholine-4-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1146596-37-3 Structure

  • Basic information

    1. Product Name: N-[(5-amino-4-cyano-3-phenyl-2,3-dihydrothiophen-2-yl)carbonyl]morpholine-4-carboxamide
    2. Synonyms:
    3. CAS NO:1146596-37-3
    4. Molecular Formula:
    5. Molecular Weight: 358.421
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1146596-37-3.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: N-[(5-amino-4-cyano-3-phenyl-2,3-dihydrothiophen-2-yl)carbonyl]morpholine-4-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[(5-amino-4-cyano-3-phenyl-2,3-dihydrothiophen-2-yl)carbonyl]morpholine-4-carboxamide(1146596-37-3)
    11. EPA Substance Registry System: N-[(5-amino-4-cyano-3-phenyl-2,3-dihydrothiophen-2-yl)carbonyl]morpholine-4-carboxamide(1146596-37-3)

  • 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: 1146596-37-3(Hazardous Substances Data)

1146596-37-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1146596-37-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,6,5,9 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1146596-37:
(9*1)+(8*1)+(7*4)+(6*6)+(5*5)+(4*9)+(3*6)+(2*3)+(1*7)=173
173 % 10 = 3
So 1146596-37-3 is a valid CAS Registry Number.

1146596-37-3Upstream product

1146596-37-3Downstream Products

1146596-37-3Relevant articles and documents

An efficient synthesis of dihydrothiophene ureidoformamides by domino reactions of 1,3-thiazolidinedione under catalyst-free conditions

Lu, Guo-Ping,Zeng, Li-Yan,Cai, Chun

, p. 998 - 1003 (2011)

An efficient synthesis of dihydrothiophene ureidoformamides by the domino reactions of aldehydes, malononitrile, amines and 1,3-thiazolidinedione in PEG 400/H2O is studied. The reaction is free of catalysts and toxic solvents, of shorter reacti

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