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80913-72-0

N-[(2,4-dichloro-phenoxy)-acetyl]-DL-aspartic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 80913-72-0 Structure

  • Basic information

    1. Product Name: N-[(2,4-dichloro-phenoxy)-acetyl]-DL-aspartic acid
    2. Synonyms:
    3. CAS NO:80913-72-0
    4. Molecular Formula:
    5. Molecular Weight: 336.128
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80913-72-0.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: N-[(2,4-dichloro-phenoxy)-acetyl]-DL-aspartic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[(2,4-dichloro-phenoxy)-acetyl]-DL-aspartic acid(80913-72-0)
    11. EPA Substance Registry System: N-[(2,4-dichloro-phenoxy)-acetyl]-DL-aspartic acid(80913-72-0)

  • 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: 80913-72-0(Hazardous Substances Data)

80913-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80913-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,1 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80913-72:
(7*8)+(6*0)+(5*9)+(4*1)+(3*3)+(2*7)+(1*2)=130
130 % 10 = 0
So 80913-72-0 is a valid CAS Registry Number.

80913-72-0Downstream Products

80913-72-0Relevant articles and documents

Hydrophobic metabolites of 2,4-dichlorophenoxyacetic acid (2,4-D) in cultured coconut tissue

López-Villalobos, Arturo,Hornung, Roland,Dodds, Peter F.

, p. 2763 - 2774 (2007/10/03)

Metabolites of 2,4-D, synthesised by coconut plumules cultured in vitro, included lipophilic chain-elongated forms with aliphatic chains of up to 16 carbons esterified to form triacylglycerol analogues. Cultures of inflorescence and plumular tissues of co

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