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(S)-tert-butyl 3-phenoxypyrrolidine-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1-Pyrrolidinecarboxylic acid, 3-phenoxy-, 1,1-dimethylethyl ester, (3S)-

    Cas No: 931409-70-0

  • USD $ 1.9-2.9 / Gram

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  • 931409-70-0 Structure
  • Basic information

    1. Product Name: (S)-tert-butyl 3-phenoxypyrrolidine-1-carboxylate
    2. Synonyms: (S)-tert-butyl 3-phenoxypyrrolidine-1-carboxylate
    3. CAS NO:931409-70-0
    4. Molecular Formula:
    5. Molecular Weight: 263.337
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 931409-70-0.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: (S)-tert-butyl 3-phenoxypyrrolidine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-tert-butyl 3-phenoxypyrrolidine-1-carboxylate(931409-70-0)
    11. EPA Substance Registry System: (S)-tert-butyl 3-phenoxypyrrolidine-1-carboxylate(931409-70-0)
  • 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: 931409-70-0(Hazardous Substances Data)

931409-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 931409-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,1,4,0 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 931409-70:
(8*9)+(7*3)+(6*1)+(5*4)+(4*0)+(3*9)+(2*7)+(1*0)=160
160 % 10 = 0
So 931409-70-0 is a valid CAS Registry Number.

931409-70-0Relevant articles and documents

Copper-catalyzed O-arylation of N-protected 1,2-aminoalcohols using functionalized trivalent organobismuth reagents

Petiot, Pauline,Dansereau, Julien,Hbert, Martin,Khene, Imene,Ahmad, Tabinda,Samaali, Samira,Leroy, Maxime,Pinsonneault, Francis,Legault, Claude Y.,Gagnon, Alexandre

, p. 1322 - 1327 (2015)

The O-arylation of 1,2-aminoalcohols using functionalized triarylbismuth reagents is reported. The reaction can be performed using substoichiometric amounts of copper acetate and operates under mild conditions. Good functional group tolerance is observed, giving access to a range of β-aryloxyamines. The effect provided by the amino group in the arylation reaction is investigated.

CARBOXAMIDE DERIVATIVES AS MUSCARINIC RECEPTOR ANTAGONISTS

-

Page/Page column 42, (2008/06/13)

The invention relates to compounds of Formula (I) processes and intermediates for their preparation, their use as muscarinic antagonists and pharmaceutical composition containing them.

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