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CAS

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406726-43-0

6-[(Furan-2-carbonyl)-amino]-hexanoic acid benzyloxy-amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 406726-43-0 Structure

  • Basic information

    1. Product Name: 6-[(Furan-2-carbonyl)-amino]-hexanoic acid benzyloxy-amide
    2. Synonyms: 6-[(Furan-2-carbonyl)-amino]-hexanoic acid benzyloxy-amide
    3. CAS NO:406726-43-0
    4. Molecular Formula:
    5. Molecular Weight: 330.384
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 406726-43-0.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: 6-[(Furan-2-carbonyl)-amino]-hexanoic acid benzyloxy-amide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-[(Furan-2-carbonyl)-amino]-hexanoic acid benzyloxy-amide(406726-43-0)
    11. EPA Substance Registry System: 6-[(Furan-2-carbonyl)-amino]-hexanoic acid benzyloxy-amide(406726-43-0)

  • 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: 406726-43-0(Hazardous Substances Data)

406726-43-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 406726-43-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,7,2 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 406726-43:
(8*4)+(7*0)+(6*6)+(5*7)+(4*2)+(3*6)+(2*4)+(1*3)=140
140 % 10 = 0
So 406726-43-0 is a valid CAS Registry Number.

406726-43-0Downstream Products

406726-43-0Relevant articles and documents

Carbamic acid compounds comprising an amide linkage as hdac inhibitors

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, (2008/06/13)

This invention pertains to certain active carbamic acid compounds which inhibit HDAC activity and which have the formula (1) wherein: A is an aryl group; Q1 is an aryl leader group having a backbone of at least 2 carbon atoms; J is an amide linkage selected from: —NR1C(═O)—and —C(═O)NR1—; R1 is an amido substituent; and, Q2 is an acid leader group; and pharmaceutically acceptable salts, solvates, amides, esters, ethers, chemically protected forms, and prodrugs thereof. The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit HDAC, and, e.g., to inhibit proliferative conditions, such as cancer and psoriasis.

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