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2-ethyl-3-4'-hydroxybenzoyl-3',5'-diiodo-5-nitrobenzofuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29735-83-9

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  • 29735-83-9 Structure

  • Basic information

    1. Product Name: 2-ethyl-3-4'-hydroxybenzoyl-3',5'-diiodo-5-nitrobenzofuran
    2. Synonyms:
    3. CAS NO:29735-83-9
    4. Molecular Formula:
    5. Molecular Weight: 563.087
    6. EINECS: N/A
    7. Product Categories: N/A

  • 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: 2-ethyl-3-4'-hydroxybenzoyl-3',5'-diiodo-5-nitrobenzofuran(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-ethyl-3-4'-hydroxybenzoyl-3',5'-diiodo-5-nitrobenzofuran(29735-83-9)
    11. EPA Substance Registry System: 2-ethyl-3-4'-hydroxybenzoyl-3',5'-diiodo-5-nitrobenzofuran(29735-83-9)

  • 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: 29735-83-9(Hazardous Substances Data)

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29735-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29735-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,3 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29735-83:
(7*2)+(6*9)+(5*7)+(4*3)+(3*5)+(2*8)+(1*3)=149
149 % 10 = 9
So 29735-83-9 is a valid CAS Registry Number.

29735-83-9Downstream Products

29735-83-9Relevant academic research and scientific papers

Antibacterial activity and polarographic half-wave reduction potential of 2-nitrobenzo[b]furans

Ohishi,Kuriyama,Doi,Nakanishi

, p. 2854 - 2861 (2007/10/02)

The antibacterial activities of a series of 2-nitrobenzo[b]furan derivatives against St. aureus, B. subtilis, E. coli, Sal. typhimurium, Sal. enteritidis, Sh. flexneri, Pr. vulgaris or Ps. aeruginosa were determined in vitro. Most of the compounds showed

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