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(2S,3S)-tert-butyl 2,3-dibenzoyl-2'-oxospiro[cyclopropane-1,3'-indoline]-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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  • 1638684-69-1 Structure
  • Basic information

    1. Product Name: (2S,3S)-tert-butyl 2,3-dibenzoyl-2'-oxospiro[cyclopropane-1,3'-indoline]-1'-carboxylate
    2. Synonyms:
    3. CAS NO:1638684-69-1
    4. Molecular Formula:
    5. Molecular Weight: 467.521
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1638684-69-1.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: (2S,3S)-tert-butyl 2,3-dibenzoyl-2'-oxospiro[cyclopropane-1,3'-indoline]-1'-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,3S)-tert-butyl 2,3-dibenzoyl-2'-oxospiro[cyclopropane-1,3'-indoline]-1'-carboxylate(1638684-69-1)
    11. EPA Substance Registry System: (2S,3S)-tert-butyl 2,3-dibenzoyl-2'-oxospiro[cyclopropane-1,3'-indoline]-1'-carboxylate(1638684-69-1)
  • 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: 1638684-69-1(Hazardous Substances Data)

1638684-69-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1638684-69-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,3,8,6,8 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1638684-69:
(9*1)+(8*6)+(7*3)+(6*8)+(5*6)+(4*8)+(3*4)+(2*6)+(1*9)=221
221 % 10 = 1
So 1638684-69-1 is a valid CAS Registry Number.

1638684-69-1Downstream Products

1638684-69-1Relevant articles and documents

Catalytic Asymmetric Synthesis of Chiral Spiro-cyclopropyl Oxindoles from 3-Alkenyl-oxindoles and Sulfoxonium Ylides

Wang, Lifeng,Cao, Weidi,Mei, Hongjiang,Hu, Linfeng,Feng, Xiaoming

supporting information, p. 4089 - 4093 (2018/10/02)

A new enantioselective cyclopropanation of 3-alkenyl-oxindoles with sulfoxonium ylides was realized by using a chiral N,N′-dioxide/Mg(OTf)2 complex as the catalyst. Various chiral spiro-cyclopropyl oxindoles containing two or three continuous chiral carbon centres were obtained in high yields (up to 99%) with good dr (up to 97:3 dr) and high ee values (up to 94% ee). (Figure presented.).

Asymmetric diastereoselective synthesis of spirocyclopropane derivatives of oxindole

Oseka, Maksim,Noole, Artur,Zari, Sergei,Oeeren, Mario,Jaerving, Ivar,Lopp, Margus,Kanger, Tonis

, p. 3599 - 3606 (2014/06/23)

A new asymmetric organocatalytic synthesis of spirocyclopropane oxindoles has been developed. The method is based on the Michael addition of N-Boc-protected 3-chlorooxindole to unsaturated 1,4-dicarbonyl compounds, affording trans-substituted spirocyclopropane oxindole derivatives in high diastereo- and enantioselectivity. Copyright

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