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N-(tert-butyldimethylsilyloxycarbonyl)-2-methoxy-5-pivaloyloxymethylpyrrolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 468097-08-7 Structure
  • Basic information

    1. Product Name: N-(tert-butyldimethylsilyloxycarbonyl)-2-methoxy-5-pivaloyloxymethylpyrrolidine
    2. Synonyms: N-(tert-butyldimethylsilyloxycarbonyl)-2-methoxy-5-pivaloyloxymethylpyrrolidine
    3. CAS NO:468097-08-7
    4. Molecular Formula:
    5. Molecular Weight: 373.565
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 468097-08-7.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: N-(tert-butyldimethylsilyloxycarbonyl)-2-methoxy-5-pivaloyloxymethylpyrrolidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(tert-butyldimethylsilyloxycarbonyl)-2-methoxy-5-pivaloyloxymethylpyrrolidine(468097-08-7)
    11. EPA Substance Registry System: N-(tert-butyldimethylsilyloxycarbonyl)-2-methoxy-5-pivaloyloxymethylpyrrolidine(468097-08-7)
  • 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: 468097-08-7(Hazardous Substances Data)

468097-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 468097-08-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,8,0,9 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 468097-08:
(8*4)+(7*6)+(6*8)+(5*0)+(4*9)+(3*7)+(2*0)+(1*8)=187
187 % 10 = 7
So 468097-08-7 is a valid CAS Registry Number.

468097-08-7Upstream product

468097-08-7Downstream Products

468097-08-7Relevant articles and documents

Efficient synthesis of (S)-3,4-dihydro-2-pivaloyloxymethyl-2H-pyrrole 1-oxide

Busque, Felix,De March, Pedro,Figueredo, Marta,Font, Josep,Gallagher, Timothy,Milan, Sergio

, p. 437 - 445 (2002)

A convenient synthesis of the title nitrone is reported. The sequence starts from ethyl L-pyroglutamate as the source of chirality and the key step is the generation of an unstable α-methoxy-N-carboxylate ion, which readily decomposes to an imine. The oxidation of the imine with methyl(trifluoromethyl)dioxirane provides the enantiopure nitrone, which is trapped with dimethyl acetylenedicarboxylate.

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