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872471-07-3

acetic acid 2-hept-1-ynyl-phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 872471-07-3 Structure

  • Basic information

    1. Product Name: acetic acid 2-hept-1-ynyl-phenyl ester
    2. Synonyms: acetic acid 2-hept-1-ynyl-phenyl ester
    3. CAS NO:872471-07-3
    4. Molecular Formula:
    5. Molecular Weight: 230.307
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 872471-07-3.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: acetic acid 2-hept-1-ynyl-phenyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: acetic acid 2-hept-1-ynyl-phenyl ester(872471-07-3)
    11. EPA Substance Registry System: acetic acid 2-hept-1-ynyl-phenyl ester(872471-07-3)

  • 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: 872471-07-3(Hazardous Substances Data)

872471-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 872471-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,4,7 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 872471-07:
(8*8)+(7*7)+(6*2)+(5*4)+(4*7)+(3*1)+(2*0)+(1*7)=183
183 % 10 = 3
So 872471-07-3 is a valid CAS Registry Number.

872471-07-3Upstream product

872471-07-3Downstream Products

872471-07-3Relevant articles and documents

Novel PdII-mediated cascade carboxylative annulation to construct benzo[b]furan-3-carboxylic acids

Liao, Yun,Smith, Jennifer,Fathi, Reza,Yang, Zhen

, p. 2707 - 2709 (2005)

(Chemical Equation Presented) Benzo[b]furan-3-carboxylic acid (2) was generated from 1 by forming three new bonds in one step via a Pd II-mediated cascade carboxylative annulation. The proposed mechanism was supported by the observation of an u

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