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(R)-(+)-tert-butyl 2-{4-[tert-butyldimethylsiloxy]methylbenzyl}pyrrolidine-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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  • 1243726-44-4 Structure
  • Basic information

    1. Product Name: (R)-(+)-tert-butyl 2-{4-[tert-butyldimethylsiloxy]methylbenzyl}pyrrolidine-1-carboxylate
    2. Synonyms:
    3. CAS NO:1243726-44-4
    4. Molecular Formula:
    5. Molecular Weight: 405.653
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1243726-44-4.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: (R)-(+)-tert-butyl 2-{4-[tert-butyldimethylsiloxy]methylbenzyl}pyrrolidine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-(+)-tert-butyl 2-{4-[tert-butyldimethylsiloxy]methylbenzyl}pyrrolidine-1-carboxylate(1243726-44-4)
    11. EPA Substance Registry System: (R)-(+)-tert-butyl 2-{4-[tert-butyldimethylsiloxy]methylbenzyl}pyrrolidine-1-carboxylate(1243726-44-4)
  • 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: 1243726-44-4(Hazardous Substances Data)

1243726-44-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1243726-44-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,3,7,2 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1243726-44:
(9*1)+(8*2)+(7*4)+(6*3)+(5*7)+(4*2)+(3*6)+(2*4)+(1*4)=144
144 % 10 = 4
So 1243726-44-4 is a valid CAS Registry Number.

1243726-44-4Downstream Products

1243726-44-4Relevant articles and documents

Asymmetric palladium-catalyzed carboamination reactions for the synthesis of enantiomerically enriched 2-(Arylmethyl)- and 2-(Alkenylmethyl)pyrrolidines

Mai, Duy N.,Wolfe, John P.

supporting information; experimental part, p. 12157 - 12159 (2010/11/03)

The enantioselective synthesis of 2-(arylmethyl)- and 2-(alkenylmethyl) pyrrolidine derivatives via Pd-catalyzed alkene carboamination reactions is described. These transformations generate enantiomerically enriched products with up to 94% ee from readily

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