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(2S)-5-Oxo-2-pyrrolidinecarbothioic Acid S-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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  • 1298024-11-9 Structure
  • Basic information

    1. Product Name: (2S)-5-Oxo-2-pyrrolidinecarbothioic Acid S-Ethyl Ester
    2. Synonyms: (2S)-5-Oxo-2-pyrrolidinecarbothioic Acid S-Ethyl Ester
    3. CAS NO:1298024-11-9
    4. Molecular Formula: C7H11NO2S
    5. Molecular Weight: 173.23274
    6. EINECS: N/A
    7. Product Categories: Heterocycles, Pharmaceuticals, Intermediates & Fine Chemicals, Sulfur & Selenium Compounds
    8. Mol File: 1298024-11-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 365.9±31.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.211±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.41±0.40(Predicted)
    10. CAS DataBase Reference: (2S)-5-Oxo-2-pyrrolidinecarbothioic Acid S-Ethyl Ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: (2S)-5-Oxo-2-pyrrolidinecarbothioic Acid S-Ethyl Ester(1298024-11-9)
    12. EPA Substance Registry System: (2S)-5-Oxo-2-pyrrolidinecarbothioic Acid S-Ethyl Ester(1298024-11-9)
  • 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: 1298024-11-9(Hazardous Substances Data)

1298024-11-9 Usage

Chemical Properties

Yellow Oil

Check Digit Verification of cas no

The CAS Registry Mumber 1298024-11-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,8,0,2 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1298024-11:
(9*1)+(8*2)+(7*9)+(6*8)+(5*0)+(4*2)+(3*4)+(2*1)+(1*1)=159
159 % 10 = 9
So 1298024-11-9 is a valid CAS Registry Number.

1298024-11-9Relevant articles and documents

AMIDE DERIVATIVE INHIBITOR AND PREPARATION METHOD AND APPLICATION THEREOF

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Paragraph 0210-0211, (2020/01/22)

An amide derivative inhibitor and a preparation method and an application thereof. Specifically relating to the compound shown in general formula (I), a preparation method for same, a pharmaceutical composition comprising said compound, and an application of same as an ASK inhibitor for the treatment of neurodegenerative disease, cardiovascular disease, inflammation, autoimmune and metabolic disease, each of the substituents in the general formula (I) being as defined in the description.

Total synthesis of (-)-sessilifoliamide C and (-)-8-epi-stemoamide

Hoye, Adam T.,Wipf, Peter

supporting information; experimental part, p. 2634 - 2637 (2011/07/09)

A convergent route featuring [3,3]-sigmatropic rearrangements of a linchpin azepinopyrrolidine served to install two of the four contiguous stereocenters present in the tricyclic Stemona alkaloids sessilifoliamide and stemoamide. In addition to the first total synthesis of (-)-sessilifoliamide C, a potential biosynthetic relationship between the sessilifoliamides and previously reported Stemona alkaloids is presented.

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