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1-Benzyl-3-Methyl-Pyrrolidine-3-Carbonitrile is a chemical compound with the molecular formula C14H16N2. It belongs to the class of pyrrolidines, which are compounds containing a pyrrolidine ring, a five-membered saturated heterocycle composed of four carbon atoms and a nitrogen atom. This organic compound has potential utility in scientific research and development, particularly in the field of synthetic chemistry. However, it is not widely studied or used, and extensive data on its usage and effects may not be readily available.

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  • 114373-05-6 Structure
  • Basic information

    1. Product Name: 1-BENZYL-3-METHYL-PYRROLIDINE-3-CARBONITRILE
    2. Synonyms: 1-BENZYL-3-METHYL-PYRROLIDINE-3-CARBONITRILE;3-Methyl-1-(phenylmethyl)-3-pyrrolidinecarbonitrile
    3. CAS NO:114373-05-6
    4. Molecular Formula: C13H16N2
    5. Molecular Weight: 200.28
    6. EINECS: N/A
    7. Product Categories: pharmacetical
    8. Mol File: 114373-05-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 315℃
    3. Flash Point: 130℃
    4. Appearance: /
    5. Density: 1.07
    6. Vapor Pressure: 0.00046mmHg at 25°C
    7. Refractive Index: 1.565
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-BENZYL-3-METHYL-PYRROLIDINE-3-CARBONITRILE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-BENZYL-3-METHYL-PYRROLIDINE-3-CARBONITRILE(114373-05-6)
    12. EPA Substance Registry System: 1-BENZYL-3-METHYL-PYRROLIDINE-3-CARBONITRILE(114373-05-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 36
    3. Safety Statements: 26
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 114373-05-6(Hazardous Substances Data)

114373-05-6 Usage

Uses

Used in Scientific Research:
1-Benzyl-3-Methyl-Pyrrolidine-3-Carbonitrile is used as a research compound for exploring its physical and chemical characteristics, toxicology, and potency in a lab setting.
Used in Synthetic Chemistry:
1-Benzyl-3-Methyl-Pyrrolidine-3-Carbonitrile is used as a building block or intermediate in the synthesis of more complex organic molecules, contributing to the development of new chemical entities and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 114373-05-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,3,7 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114373-05:
(8*1)+(7*1)+(6*4)+(5*3)+(4*7)+(3*3)+(2*0)+(1*5)=96
96 % 10 = 6
So 114373-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H16N2/c1-13(10-14)7-8-15(11-13)9-12-5-3-2-4-6-12/h2-6H,7-9,11H2,1H3

114373-05-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Benzyl-3-methylpyrrolidine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 1-benzyl-3-methylpyrrolidine-3-carbonitrile

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:114373-05-6 SDS

114373-05-6Relevant articles and documents

[3+2] Dipolar cycloadditions of an unstabilised azomethine ylide under continuous flow conditions

Grafton, Mark,Mansfield, Andrew C.,Fray, M. Jonathan

scheme or table, p. 1026 - 1029 (2010/04/02)

The [3+2] dipolar cycloaddition reactions of the unstabilised azomethine ylide precursor benzyl(methoxymethyl)(trimethylsilylmethyl)amine with 12 electron-deficient alkenes in the presence of catalytic trifluoroacetic acid are examined under continuous fl

New quinolone antibacterial agents. Synthesis and biological activity of 7-(3,3- or 3,4-disubstituted-1-pyrrolidinyl)quinoline-3-carboxylic acids

Hagen,Domagala,Heifetz,Sanchez,Solomon

, p. 849 - 854 (2007/10/02)

A series of 7-(3-amino- or 3-aminomethyl-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro- 4-oxo-3-quinolinecarboxylic acids was synthesized and tested for antibacterial activity. Unique to these quinolones was the presence of a methyl or phenyl gro

7-[[3-(aminomethyl)-3-alkyl]-1-pyrrolidinyl]-quinoline-carboxylic acids

-

, (2008/06/13)

Novel, orally active antibacterial agents are described and characterized as 7-[[3-(aminomethyl)-3-alkyl]-1-pyrrolidinyl]-6-fluoro-1,4-dihydro-4-oxo-3-quinoline carboxylic acids or corresponding 1,8-naphthyridine derivatives as well as methods for their m

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