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CAS

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865362-95-4

(1R,3S)-1-(1-phenyl-ethyl)-5-thioxo-pyrrolidine-3-carboxylic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 865362-95-4 Structure

  • Basic information

    1. Product Name: (1R,3S)-1-(1-phenyl-ethyl)-5-thioxo-pyrrolidine-3-carboxylic acid methyl ester
    2. Synonyms: (1R,3S)-1-(1-phenyl-ethyl)-5-thioxo-pyrrolidine-3-carboxylic acid methyl ester
    3. CAS NO:865362-95-4
    4. Molecular Formula:
    5. Molecular Weight: 263.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 865362-95-4.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: (1R,3S)-1-(1-phenyl-ethyl)-5-thioxo-pyrrolidine-3-carboxylic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,3S)-1-(1-phenyl-ethyl)-5-thioxo-pyrrolidine-3-carboxylic acid methyl ester(865362-95-4)
    11. EPA Substance Registry System: (1R,3S)-1-(1-phenyl-ethyl)-5-thioxo-pyrrolidine-3-carboxylic acid methyl ester(865362-95-4)

  • 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: 865362-95-4(Hazardous Substances Data)

865362-95-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 865362-95-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,5,3,6 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 865362-95:
(8*8)+(7*6)+(6*5)+(5*3)+(4*6)+(3*2)+(2*9)+(1*5)=204
204 % 10 = 4
So 865362-95-4 is a valid CAS Registry Number.

865362-95-4Relevant articles and documents

A rapid and convenient synthesis of β-proline

Blanchet, Jér?me,Pouliquen, Mickael,Lasne, Marie-Claire,Rouden, Jacques

, p. 5727 - 5730 (2008/02/09)

A short, reliable, and cheap synthesis of both enantiomers of β-proline, an efficient organocatalyst and an important building block in medicinal chemistry, has been developed in four steps (overall yield: 72%) from the diasteromeric adducts of methyl itaconate and (R)-α-methylbenzylamine. The key step involves the chemoselective reduction of a lactam group in the presence of a benzyl ester.

A convenient and new approach to the synthesis of ω-heterocyclic amino acids from carboxy lactams through ring-chain-transformation. Part 2: Synthesis of (2R)-/(2S)-2-aminomethyl-3-(1-aryl-/1,5-diaryl-1H-pyrazol-3-yl)- propionic acid

Singh, Rakesh K.,Sinha, Neelima,Jain, Sanjay,Salman, Mohammad,Naqvi, Fehmida,Anand, Nitya

, p. 8868 - 8874 (2007/10/03)

Making use of amide activation, a convenient and short path synthesis of optically pure ω-heterocyclic-β-amino acids has been achieved from (1R,3R)- and (1R,3S)-5-oxo-1-(1-phenyl-ethyl)-pyrrolidine-3-carboxylic acid methyl ester. The key step of the synth

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