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CAS

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1188543-05-6

methanesulfonic acid 1-[5-oxo-1-(3-trifluoromethylphenyl)pyrrolidin-3-yl]ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1188543-05-6 Structure

  • Basic information

    1. Product Name: methanesulfonic acid 1-[5-oxo-1-(3-trifluoromethylphenyl)pyrrolidin-3-yl]ethyl ester
    2. Synonyms: methanesulfonic acid 1-[5-oxo-1-(3-trifluoromethylphenyl)pyrrolidin-3-yl]ethyl ester
    3. CAS NO:1188543-05-6
    4. Molecular Formula:
    5. Molecular Weight: 351.347
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1188543-05-6.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: methanesulfonic acid 1-[5-oxo-1-(3-trifluoromethylphenyl)pyrrolidin-3-yl]ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: methanesulfonic acid 1-[5-oxo-1-(3-trifluoromethylphenyl)pyrrolidin-3-yl]ethyl ester(1188543-05-6)
    11. EPA Substance Registry System: methanesulfonic acid 1-[5-oxo-1-(3-trifluoromethylphenyl)pyrrolidin-3-yl]ethyl ester(1188543-05-6)

  • 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: 1188543-05-6(Hazardous Substances Data)

1188543-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1188543-05-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,8,5,4 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1188543-05:
(9*1)+(8*1)+(7*8)+(6*8)+(5*5)+(4*4)+(3*3)+(2*0)+(1*5)=176
176 % 10 = 6
So 1188543-05-6 is a valid CAS Registry Number.

1188543-05-6Relevant articles and documents

A2Badenosine receptor antagonists: Design, synthesis and biological evaluation of novel xanthine derivatives

Basu, Sujay,Barawkar, Dinesh A.,Ramdas, Vidya,Waman, Yogesh,Patel, Meena,Panmand, Anil,Kumar, Santosh,Thorat, Sachin,Bonagiri, Rajesh,Jadhav, Dilip,Mukhopadhyay, Partha,Prasad, Vandna,Reddy, B. Srinivasa,Goswami, Arnab,Chaturvedi, Sandhya,Menon, Suraj,Quraishi, Azfar,Ghosh, Indraneel,Dusange, Sushant,Paliwal, Shalini,Kulkarni, Abhay,Karande, Vikas,Thakre, Rhishikesh,Bedse, Gaurav,Rouduri, Sreekanth,Gundu, Jayasagar,Palle, Venkata P.,Chugh, Anita,Mookhtiar, Kasim A.

, p. 986 - 996 (2017/02/12)

A2BAdoR is a low affinity adenosine receptor that functions by Gs mediated elevation of cAMP and subsequent downstream signaling. The receptor has been implicated in lung inflammatory disorders like?COPD and asthma. Several potent and selective

HETEROCYCLIC COMPOUNDS AS ADENOSINE RECEPTOR ANTAGONIST

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Page/Page column 109, (2009/10/22)

Compounds of the present disclosure are fused pyrimidine compounds of formula (I), its tautomers, polymorphs, stereoisomers, prodrugs, solvate or a pharmaceutically acceptable salts thereof, as Adenosine receptor antagonists. Processes of their preparation are also described in the disclosure.

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