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76327-34-9

3-chloro-4-(heptyloxy)benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76327-34-9 Structure

  • Basic information

    1. Product Name: 3-chloro-4-(heptyloxy)benzoic acid
    2. Synonyms:
    3. CAS NO:76327-34-9
    4. Molecular Formula:
    5. Molecular Weight: 270.756
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76327-34-9.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: 3-chloro-4-(heptyloxy)benzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-chloro-4-(heptyloxy)benzoic acid(76327-34-9)
    11. EPA Substance Registry System: 3-chloro-4-(heptyloxy)benzoic acid(76327-34-9)

  • 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: 76327-34-9(Hazardous Substances Data)

76327-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76327-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,2 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76327-34:
(7*7)+(6*6)+(5*3)+(4*2)+(3*7)+(2*3)+(1*4)=139
139 % 10 = 9
So 76327-34-9 is a valid CAS Registry Number.

76327-34-9Downstream Products

76327-34-9Relevant articles and documents

Amphipathic benzoic acid derivatives: Synthesis and binding in the hydrophobic tunnel of the zinc deacetylase LpxC

Shin, Hyunshun,Gennadios, Heather A.,Whittington, Douglas A.,Christianson, David W.

, p. 2617 - 2623 (2007)

The first committed step in lipid A biosynthesis is catalyzed by uridine diphosphate-(3-O-(R-3-hydroxymyristoyl))-N-acetylglucosamine deacetylase (LpxC), a zinc-dependent deacetylase, and inhibitors of LpxC may be useful in the development of antibacteria

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