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1-Pyrrolidinamine, N-(phenylmethylene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60144-33-4

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60144-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60144-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,4 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60144-33:
(7*6)+(6*0)+(5*1)+(4*4)+(3*4)+(2*3)+(1*3)=84
84 % 10 = 4
So 60144-33-4 is a valid CAS Registry Number.

60144-33-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-N-pyrrolidin-1-ylmethanimine

1.2 Other means of identification

Product number -
Other names benzaldehyde N,N-tetramethylenehydrazone

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:60144-33-4 SDS

60144-33-4Relevant academic research and scientific papers

Continuous Flow α-Arylation of N,N-Dialkylhydrazones under Visible-Light Photoredox Catalysis

Vega, Juan A.,Alonso, José Manuel,Méndez, Gabriela,Ciordia, Myriam,Delgado, Francisca,Trabanco, Andrés A.

supporting information, p. 938 - 941 (2017/02/26)

The first direct α-arylation of aldehyde-derived N,N-dialkylhydrazones with electron deficient aryl and heteroaryl cyanides under visible-light photoredox catalysis has been developed. Structurally complex α,α′-diaryl-N,N-cycloalkylhydrazones were obtaine

Asymmetrie imino aza-enamine reaction catalyzed by axially chiral dicarboxylic acid: Use of arylaldehyde N,N-dialkylnydrazones as acyl anion equivalent

Hashimoto, Takuya,Hirose, Maya,Maruoka, Keiji

, p. 7556 - 7557 (2008/12/22)

Synthetic utility of arylaldehyde N,N-dialkylhydrazones as a practical acyl anion equivalent could be exploited for the first time in the asymmetric imino aza-enamine reaction catalyzed by axially chiral carboxylic acid. Copyright

An enantioselective chiral Bronsted acid catalyzed imino-azaenamine reaction

Rueping, Magnus,Sugiono, Erli,Theissmann, Thomas,Kuenkel, Alexander,Kockritz, Angela,Pews-Davtyan, Anahit,Nemati, Navid,Beller, Matthias

, p. 1065 - 1068 (2007/10/03)

(Chemical Equation Presented) The enantioselective Bronsted acid catalyzed addition of methyleneaminopyrrolidine to N-Boc imines has been achieved in the presence of chiral phosphoric acids derived from 3,3′-di(phenanthryl)-H8-BINOL. The corresponding ami

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