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178424-13-0

1,7-heptanediylbis(4-benzonitrile) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 178424-13-0 Structure

  • Basic information

    1. Product Name: 1,7-heptanediylbis(4-benzonitrile)
    2. Synonyms:
    3. CAS NO:178424-13-0
    4. Molecular Formula:
    5. Molecular Weight: 302.419
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 178424-13-0.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: 1,7-heptanediylbis(4-benzonitrile)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,7-heptanediylbis(4-benzonitrile)(178424-13-0)
    11. EPA Substance Registry System: 1,7-heptanediylbis(4-benzonitrile)(178424-13-0)

  • 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: 178424-13-0(Hazardous Substances Data)

178424-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 178424-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,4,2 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 178424-13:
(8*1)+(7*7)+(6*8)+(5*4)+(4*2)+(3*4)+(2*1)+(1*3)=150
150 % 10 = 0
So 178424-13-0 is a valid CAS Registry Number.

178424-13-0Downstream Products

178424-13-0Relevant articles and documents

Synthesis and trypanocidal activity of the bis-carba analogue of pentamidine

Zhang,Berger,Ulrich

, p. 1035 - 1036 (1996)

Because toxic metabolites are formed by microsomal oxidative cleavage of the ether methylenes of the antiprotozoal drug, pentamidine, we synthesized the previoulsy unreported analogue of pentamidine in which the ether oxygens are replaced by methylenes. Although this compound was about 20-fold less active than pentamidine against Trypanosoma brucei infection in mice, it did not undergo oxidative cleavage, suggesting a new direction for design of less toxic pentamidine analogues.

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