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3-benzyl-1-methylpyrrolidine-2,5-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105909-88-4 Structure
  • Basic information

    1. Product Name: 3-benzyl-1-methylpyrrolidine-2,5-dione
    2. Synonyms:
    3. CAS NO:105909-88-4
    4. Molecular Formula: C12H13NO2
    5. Molecular Weight: 203.2371
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105909-88-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 355.1°C at 760 mmHg
    3. Flash Point: 161.6°C
    4. Appearance: N/A
    5. Density: 1.188g/cm3
    6. Vapor Pressure: 3.2E-05mmHg at 25°C
    7. Refractive Index: 1.57
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-benzyl-1-methylpyrrolidine-2,5-dione(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-benzyl-1-methylpyrrolidine-2,5-dione(105909-88-4)
    12. EPA Substance Registry System: 3-benzyl-1-methylpyrrolidine-2,5-dione(105909-88-4)
  • 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: 105909-88-4(Hazardous Substances Data)

105909-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105909-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,0 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 105909-88:
(8*1)+(7*0)+(6*5)+(5*9)+(4*0)+(3*9)+(2*8)+(1*8)=134
134 % 10 = 4
So 105909-88-4 is a valid CAS Registry Number.

105909-88-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzyl-1-methylpyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names 3-Benzyl-1-methyl-pyrrolidin-2,5-dion

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:105909-88-4 SDS

105909-88-4Downstream Products

105909-88-4Relevant articles and documents

Metal-free desilylative C-C bond formation by visible-light photoredox catalysis

Uygur, Mustafa,Danelzik, Tobias,García Manche?o, Olga

supporting information, p. 2980 - 2983 (2019/03/26)

A newly developed methodology for the use of organosilanes as radical precursors under metal-free and visible-light conditions is presented. The strong oxidant character of the 9-mesityl-10-methylacridinium salt in its excited state enables the transforma

Decatungstate photocatalyzed benzylation of alkenes with alkylaromatics

Qrareya, Hisham,Ravelli, Davide,Fagnoni, Maurizio,Albini, Angelo

supporting information, p. 2891 - 2899 (2014/03/21)

The direct benzylation of electrophilic al-kenes with alkylbenzenes has been achieved by decatungstate photocatalysis in a high ionic strength medium (5:1 acetonitrile/water mixed solvents, 0.5 M lithium perchlorate). The reaction has been extended to ring-substituted (Cl, F, CN) toluenes and further alkylbenzenes. Intramolecular selectivity (p-cymene, 4-methylanisole) and deuteration effects support the atom transfer character of the process that, however, requires a sufficient stabilization of the intermediate polar exciplex to occur. The reactivity of the deca-tungstate anion is compared with that of aromatic ketones, the benchmark of photochemical hydrogen/ electron transfer processes.

Decatungstate as photoredox catalyst: Benzylation of electron-poor olefins

Montanaro, Sara,Ravelli, Davide,Merli, Daniele,Fagnoni, Maurizio,Albini, Angelo

supporting information; experimental part, p. 4218 - 4221 (2012/09/22)

Excited tetrabutylammonium decatungstate (TBADT), known to activate a variety of compounds via hydrogen atom transfer (HAT), has now been applied as a photoredox catalyst for the effective oxidative cleavage of benzyl silanes and radical benzylation of reducible olefins occurring in isolated yields from poor to excellent.

A practical method for the reductive cleavage of the sulfide bond in xanthates

Liard, Annie,Quiclet-Sire, Beatrice,Zard, Samir Z.

, p. 5877 - 5880 (2007/10/03)

Xanthates can be reduced to the corresponding alkane through cleavage of the sulfide bond by heating in 2-propanol in the presence of equimolar amounts of dilauroyl peroxide, added in small portions.

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