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128729-97-5

Pyrrolidine, 1-butyl-2-[(phenylseleno)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 128729-97-5 Structure

  • Basic information

    1. Product Name: Pyrrolidine, 1-butyl-2-[(phenylseleno)methyl]-
    2. Synonyms:
    3. CAS NO:128729-97-5
    4. Molecular Formula: C15H23NSe
    5. Molecular Weight: 296.314
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 128729-97-5.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: Pyrrolidine, 1-butyl-2-[(phenylseleno)methyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyrrolidine, 1-butyl-2-[(phenylseleno)methyl]-(128729-97-5)
    11. EPA Substance Registry System: Pyrrolidine, 1-butyl-2-[(phenylseleno)methyl]-(128729-97-5)

  • 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: 128729-97-5(Hazardous Substances Data)

128729-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128729-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,7,2 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 128729-97:
(8*1)+(7*2)+(6*8)+(5*7)+(4*2)+(3*9)+(2*9)+(1*7)=165
165 % 10 = 5
So 128729-97-5 is a valid CAS Registry Number.

128729-97-5Downstream Products

128729-97-5Relevant articles and documents

N-HYDROXYPYRIDINE-2-THIONE CARBAMATES. VI. FUNCTIONALIZATION OF CARBON RADICALS FORMED BY AMINIUM CATION RADICAL CYCLIZATIONS

Newcomb, Martin,Marquardt, Donald J.,Kumar, M. Udaya

, p. 2345 - 2352 (1990)

A variety of reagents have been evaluated for trapping carbon radicals formed from aminium cation radical cyclizations.Rapid "self-trapping" of these radicals by their PTOC carbamate precursors requires highly reactive trapping agents.Synthetically useful

N-HYDROXYPYRIDINE-2-THIONE CARBAMATES. IV. A COMPARISON OF 5-EXO CYCLIZATIONS OF AN AMINYL RADICAL AND AN AMINIUM CATION RADICAL

Newcomb, Martin,Deeb, Thomas M.,Marquardt, Donald J.

, p. 2317 - 2328 (1990)

Cyclizations of the N-butyl-4-pentenaminyl radical and the N-butyl-4-pentenaminium cation radical were studied.The radicals were produced in chain reactions from the same N-hydroxypyridine-2-thione carbamate precursors.Rate constants for cyclization of the aminyl radical and ring opening of the product thus formed at 50 deg C were determined.Cyclizations of the aminium cation radical, formed by protonation of the aminyl radical, were studied under a variety of conditions.

LEWIS ACID ACTIVATED AND CATALYZED CYCLIZATIONS OF AMINYL RADICALS FROM N-HYDROXYPYRIDINE-2-THIONE CARBAMATES

Newcomb, Martin,Ha, Chau

, p. 6493 - 6496 (1991)

A variety of Lewis acids promote 5-exo cyclizations of δ,ε-unsaturated aminyl radicals produced from N-hydroxypyridine-2-thione carbamates under very mild conditions; catalysis was demonstrated in several cases.

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