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1220283-74-8

(+/-)-tert-butyl 2-[(1-benzyl-1H-indol-5-yl)methyl]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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  • 1220283-74-8 Structure

  • Basic information

    1. Product Name: (+/-)-tert-butyl 2-[(1-benzyl-1H-indol-5-yl)methyl]pyrrolidine-1-carboxylate
    2. Synonyms: (+/-)-tert-butyl 2-[(1-benzyl-1H-indol-5-yl)methyl]pyrrolidine-1-carboxylate
    3. CAS NO:1220283-74-8
    4. Molecular Formula:
    5. Molecular Weight: 390.525
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1220283-74-8.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: (+/-)-tert-butyl 2-[(1-benzyl-1H-indol-5-yl)methyl]pyrrolidine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-tert-butyl 2-[(1-benzyl-1H-indol-5-yl)methyl]pyrrolidine-1-carboxylate(1220283-74-8)
    11. EPA Substance Registry System: (+/-)-tert-butyl 2-[(1-benzyl-1H-indol-5-yl)methyl]pyrrolidine-1-carboxylate(1220283-74-8)

  • 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: 1220283-74-8(Hazardous Substances Data)

1220283-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1220283-74-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,0,2,8 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1220283-74:
(9*1)+(8*2)+(7*2)+(6*0)+(5*2)+(4*8)+(3*3)+(2*7)+(1*4)=108
108 % 10 = 8
So 1220283-74-8 is a valid CAS Registry Number.

1220283-74-8Downstream Products

1220283-74-8Relevant articles and documents

Use of aryl chlorides as electrophiles in Pd-catalyzed alkene difunctionalization reactions

Rosen, Brandon R.,Ney, Joshua E.,Wolfe, John P.

supporting information; experimental part, p. 2756 - 2759 (2010/07/08)

The development of conditions that allow use of inexpensive aryl chlorides as electrophiles in Pd-catalyzed alkene carboamination and carboetherification reactions is described. A catalyst composed of Pd(OAc)2 and S-Phos minimizes N-arylation of the substrate and prevents formation of mixtures of regioisomeric products. A number of heterocycles, including pyrrolidines, isoxazolidines, tetrahydrofurans, and pyrazolidines, are efficiently generated with this method.

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