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4-[4-methoxy-3-nitrophenyl]-4-oxobutanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 26976-83-0 Structure
  • Basic information

    1. Product Name: 4-[4-methoxy-3-nitrophenyl]-4-oxobutanoic acid
    2. Synonyms: 4-[4-methoxy-3-nitrophenyl]-4-oxobutanoic acid
    3. CAS NO:26976-83-0
    4. Molecular Formula:
    5. Molecular Weight: 253.211
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 26976-83-0.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: 4-[4-methoxy-3-nitrophenyl]-4-oxobutanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-[4-methoxy-3-nitrophenyl]-4-oxobutanoic acid(26976-83-0)
    11. EPA Substance Registry System: 4-[4-methoxy-3-nitrophenyl]-4-oxobutanoic acid(26976-83-0)
  • 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: 26976-83-0(Hazardous Substances Data)

26976-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26976-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,7 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 26976-83:
(7*2)+(6*6)+(5*9)+(4*7)+(3*6)+(2*8)+(1*3)=160
160 % 10 = 0
So 26976-83-0 is a valid CAS Registry Number.

26976-83-0Relevant articles and documents

3(2H)-furanones promising candidates for synthesis of new fluorescent organic probes

Soliman, Mohamed H. A.,Hussein, Belal H. M.,Abdel-Moati, Nahla,El-Tamany, El-Sayed H. M.

, p. 567 - 575 (2019/05/21)

Several novel 3-arylidene-5-(4-memoxy-3-nitrophenyl)-2(3H)-furanones (2a-d) have been successfully prepared and used as precursors for building up of other new heterocyclic architectures such as pyrrolones (4a-c), (5) and unsaturated aroyl-hydrazides (7a-d). These aroyl-hydrazides have been subsequently converted into pyridazinone derivatives (8a-d) by refluxing in HCl/AcOH mixture. Eventually, benzoylation of the hydrazides (7a-c) with benzoyl chloride affords the corresponding N-benzoyl-3(2H)-pyridazinones (9a-c). The structures of all synthesized compounds have been established using elemental analysis and spectral methods. The photophysical (fluorescence and electronic absorption spectra) properties of newly synthesized compounds have also been investigated.

4-phenyl-4-oxo-butanoic acid derivatives with kynurenine-3-hydroxylase inhibiting activity

-

, (2008/06/13)

4-phenyl-4-oxo-butanoic acid derivatives for use in the treatment of the human or animal body by therepy; particularly as kynurenine-3-hydroxylase inhibitors, in the prevention and/or treatment of a neurodegenerative disease wherein the inhibition of such an enyzme is needed. The present invention further comprises a selected class of the above mentioned 4-phenyl-4-oxo-butanoic acid derivatives, their pharmaceutically acceptable salts, a process for their preparation and pharmaceutical compositions containing them.

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