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(Z)-4-oxo-4-((4-phenylthiazol-2(3H)-ylidene)amino)butanoic acid is a complex chemical compound belonging to the class of thiazole derivatives. It is characterized by the presence of a thiazole ring with an attached phenyl group, a carboxylic acid group, and a ketone functional group. (Z)-4-oxo-4-((4-phenylthiazol-2(3H)-ylidene)amino)butanoic acid's name also indicates a specific geometric configuration (Z) around the double bond, which may influence its chemical properties and potential applications.

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  • 71576-04-0 Structure
  • Basic information

    1. Product Name: (Z)-4-oxo-4-((4-phenylthiazol-2(3H)-ylidene)amino)butanoic acid
    2. Synonyms: (Z)-4-oxo-4-((4-phenylthiazol-2(3H)-ylidene)amino)butanoic acid;4-oxo-4-((4-phenylthiazol-2-yl)amino)butanoic acid
    3. CAS NO:71576-04-0
    4. Molecular Formula: C13H12N2O3S
    5. Molecular Weight: 276.31098
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 71576-04-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 510.4°C at 760 mmHg
    3. Flash Point: 262.5°C
    4. Appearance: /
    5. Density: 1.394g/cm3
    6. Vapor Pressure: 3.06E-11mmHg at 25°C
    7. Refractive Index: 1.651
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (Z)-4-oxo-4-((4-phenylthiazol-2(3H)-ylidene)amino)butanoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: (Z)-4-oxo-4-((4-phenylthiazol-2(3H)-ylidene)amino)butanoic acid(71576-04-0)
    12. EPA Substance Registry System: (Z)-4-oxo-4-((4-phenylthiazol-2(3H)-ylidene)amino)butanoic acid(71576-04-0)
  • 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: 71576-04-0(Hazardous Substances Data)

71576-04-0 Usage

Uses

Used in Pharmaceutical Applications:
(Z)-4-oxo-4-((4-phenylthiazol-2(3H)-ylidene)amino)butanoic acid is used as a potential therapeutic agent for various medical conditions due to its unique chemical structure and functional groups. Its thiazole and phenyl moieties may allow for interactions with specific biological targets, making it a candidate for drug development.
Used in Agricultural Applications:
In the agricultural industry, (Z)-4-oxo-4-((4-phenylthiazol-2(3H)-ylidene)amino)butanoic acid may be utilized as a component in the development of novel pesticides or herbicides. Its chemical structure could potentially enable it to target specific pests or weeds, providing a more efficient and environmentally friendly solution.
Used in Materials Science:
(Z)-4-oxo-4-((4-phenylthiazol-2(3H)-ylidene)amino)butanoic acid could also find applications in the field of materials science, where its unique properties may be harnessed to create new materials with specific characteristics. These materials could be used in various industries, such as electronics, automotive, or aerospace, depending on the compound's properties.

Check Digit Verification of cas no

The CAS Registry Mumber 71576-04-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,7 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71576-04:
(7*7)+(6*1)+(5*5)+(4*7)+(3*6)+(2*0)+(1*4)=130
130 % 10 = 0
So 71576-04-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N2O3S/c16-11(6-7-12(17)18)15-13-14-10(8-19-13)9-4-2-1-3-5-9/h1-5,8H,6-7H2,(H,17,18)(H,14,15,16)

71576-04-0Downstream Products

71576-04-0Relevant articles and documents

Design, synthesis, biological evaluation, and docking study of novel dual-acting thiazole-pyridiniums inhibiting acetylcholinesterase and β-amyloid aggregation for Alzheimer's disease

Ghotbi, Golaleh,Mahdavi, Mohammad,Najafi, Zahra,Moghadam, Farshad Homayouni,Hamzeh-Mivehroud, Maryam,Davaran, Soodabeh,Dastmalchi, Siavoush

, (2020)

New compounds containing thiazole and pyridinium moieties were designed and synthesized. The potency of the synthesized compounds as selective inhibitors of acetylcholinesterase (AChE), and β-amyloid aggregation (Aβ) was evaluated. Compounds 7d and 7j sho

Novel multipotent phenylthiazole-tacrine hybrids for the inhibition of cholinesterase activity, β-amyloid aggregation and Ca2+ overload

Wang, Yue,Wang, Fang,Guan, Xin-Lei,Wang, Can-Ming,Cao, Hui,Li, Ming-Xing,Chen, Jian-Guo,Jiang, Feng-Chao,Li, Lei,Yu, Jun-Ping

, p. 6513 - 6522,10 (2012/12/11)

In this study, a series of multipotent phenylthiazole-tacrine hybrids (7a-7e, 8, and 9a-9m) were synthesized and biologically evaluated. Screening results showed that phenylthiazole-tacrine hybrids were potent cholinesterase inhibitors with pIC50/su

Novel multipotent phenylthiazole-tacrine hybrids for the inhibition of cholinesterase activity, β-amyloid aggregation and Ca2+ overload

Wang, Yue,Wang, Fang,Yu, Jun-Ping,Jiang, Feng-Chao,Guan, Xin-Lei,Wang, Can-Ming,Li, Lei,Cao, Hui,Li, Ming-Xing,Chen, Jian-Guo

, p. 6513 - 6522 (2013/01/14)

In this study, a series of multipotent phenylthiazole-tacrine hybrids (7a-7e, 8, and 9a-9m) were synthesized and biologically evaluated. Screening results showed that phenylthiazole-tacrine hybrids were potent cholinesterase inhibitors with pIC50/su

Immunoactivators derived from amino thiazoles

-

, (2008/06/13)

The present invention concerns new derivatives of 4-phenyl 2-amino thiazole of the formula STR1 in which X represents a hydrogen atom, a halogen, a lower alkyl or an alkoxy, R is a hydrogen, a haloalkoxy, a substituted or unsubstituted aryl, a pyridyl, an aryloxy or a carboxy alkyl, having immunomodulating properties, useful in the treatment of rheumatoid arthritis and other ailments requiring immunotherapy.

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