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BETA-OXO-4-FLUORO-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 502424-52-4 Structure
  • Basic information

    1. Product Name: BETA-OXO-4-FLUORO-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER
    2. Synonyms: BETA-OXO-4-FLUORO-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER;tert-Butyl b-oxo-4-fluoro-benzenepropanoate
    3. CAS NO:502424-52-4
    4. Molecular Formula: C13H15FO3
    5. Molecular Weight: 238.257
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 502424-52-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: BETA-OXO-4-FLUORO-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: BETA-OXO-4-FLUORO-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER(502424-52-4)
    11. EPA Substance Registry System: BETA-OXO-4-FLUORO-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER(502424-52-4)
  • 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: 502424-52-4(Hazardous Substances Data)

502424-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 502424-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,2,4,2 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 502424-52:
(8*5)+(7*0)+(6*2)+(5*4)+(4*2)+(3*4)+(2*5)+(1*2)=104
104 % 10 = 4
So 502424-52-4 is a valid CAS Registry Number.

502424-52-4Relevant articles and documents

Phase-Transfer Catalyzed Asymmetric [4 + 1] Annulations for the Synthesis of Chiral 2,2-Disubstituted Tetrahydrothiophenes

Yin, Qi,Wen, Xiaolu,Chen, Yiwei,Gong, Xiangnan,Hu, Lin

, p. 7529 - 7534 (2021/10/02)

An efficient catalytic asymmetric [4 + 1] reaction, which features the use of simple β-keto esters as one-carbon nucleophiles and 5-succinimidothio-pent-2-enoates as four-atom bielectrophiles, has been developed in the presence of a bifunctional chiral ph

Design, synthesis and RON receptor tyrosine kinase inhibitory activity of new head groups analogs of LCRF-0004

Raeppel, Franck,Raeppel, Stéphane L.,Therrien, Eric

, p. 3810 - 3815 (2015/08/24)

New heteroarylcarboxamide head groups substituted with two aromatic rings analogs of thieno[3,2-b]pyridine-based kinase inhibitor LCRF-0004 were designed and synthesized. Potent inhibitors of RON tyrosine kinase with various level of selectivity for c-Met RTK were obtained.

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