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117034-26-1

N-cyclohexyl-1,3-benzodioxole-5-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 117034-26-1 Structure

  • Basic information

    1. Product Name: N-cyclohexyl-1,3-benzodioxole-5-carboxamide
    2. Synonyms: N-cyclohexyl-1,3-benzodioxole-5-carboxamide
    3. CAS NO:117034-26-1
    4. Molecular Formula: C14H17NO3
    5. Molecular Weight: 247.28968
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 117034-26-1.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-cyclohexyl-1,3-benzodioxole-5-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-cyclohexyl-1,3-benzodioxole-5-carboxamide(117034-26-1)
    11. EPA Substance Registry System: N-cyclohexyl-1,3-benzodioxole-5-carboxamide(117034-26-1)

  • 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: 117034-26-1(Hazardous Substances Data)

117034-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117034-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,0,3 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 117034-26:
(8*1)+(7*1)+(6*7)+(5*0)+(4*3)+(3*4)+(2*2)+(1*6)=91
91 % 10 = 1
So 117034-26-1 is a valid CAS Registry Number.

117034-26-1Downstream Products

117034-26-1Relevant articles and documents

Research on antiviral agents. 4. Studies on the chemistry of 6-methyl-2-methoxy-4-O-acyloxy and 6-methyl-2,4-di-O-acyloxypyrimidine derivatives as new acylation reagents and inhibitors of uracil DNA glycosylases.

Botta,Saladino,Gentile,Summa,Nicoletti,Verri,Focher,Spadari

, p. 3603 - 3618 (2007/10/02)

The synthesis of 6-methyl-2-methoxy-4-O-acyloxy and 6-methyl-2,4-di-O-acyloxypyrimidine derivatives 2 and 5 along with their properties as acylating agents of amines, alcohols, thiols and α-amino acids have been reported. Interestingly some of the title products revealed an inhibitory activity against the human and herpetic DNA glycosylases.

6-ALKYL-2-METHOXY-4-(3H)-PYRIMIDINONES IN THE TRANSFORMATION OF PYRIMIDINES: REGIOSPECIFIC PREPARATION, ANTITUMOR AND ANTIMICROBIAL ACTIVITY OF 4-O-ACYLATED PYRIMIDINE DERIVATIVES. NEW AGENTS FOR SELECTIVE ACYLATION OF AMINES.

Botta, Maurizio,Angelis, Francesco De,Nicoletti, Rosario,Pani, Alessandra,Marongiu, Maria Elena,Colla, Paolo La

, p. 2741 - 2744 (2007/10/02)

A high yielding synthesis of 4-O-acylated pyrimidines is presented.These products are selective reagents for amine acylation.The antitumor and antimicrobial activity of compounds 1 and 2c is also reported.

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