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acetic acid 5-nitro-2-pent-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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  • 504421-99-2 Structure
  • Basic information

    1. Product Name: acetic acid 5-nitro-2-pent-1-ynyl-phenyl ester
    2. Synonyms: acetic acid 5-nitro-2-pent-1-ynyl-phenyl ester
    3. CAS NO:504421-99-2
    4. Molecular Formula:
    5. Molecular Weight: 247.251
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 504421-99-2.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 5-nitro-2-pent-1-ynyl-phenyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: acetic acid 5-nitro-2-pent-1-ynyl-phenyl ester(504421-99-2)
    11. EPA Substance Registry System: acetic acid 5-nitro-2-pent-1-ynyl-phenyl ester(504421-99-2)
  • 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: 504421-99-2(Hazardous Substances Data)

504421-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 504421-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,4,4,2 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 504421-99:
(8*5)+(7*0)+(6*4)+(5*4)+(4*2)+(3*1)+(2*9)+(1*9)=122
122 % 10 = 2
So 504421-99-2 is a valid CAS Registry Number.

504421-99-2Downstream Products

504421-99-2Relevant articles and documents

Chemistry of aminophenols. Part 3: First synthesis of nitrobenzo[b]furans via a coupling-cyclization approach

Dai, Wei-Min,Lai, Kwong Wah

, p. 9377 - 9380 (2007/10/03)

The first synthesis of 4-, 5-, and 6-nitrobenzo[b]furans has been achieved via the Sonogashira cross-coupling reaction of 2-iodonitrophenol acetates prepared from commercially available and inexpensive 2-aminonitrophenols. The obtained 2-alkynylnitropheno

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