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Benzenamine, N-[1-(3-pyridinyl)ethylidene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

121133-22-0

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121133-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121133-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,1,3 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 121133-22:
(8*1)+(7*2)+(6*1)+(5*1)+(4*3)+(3*3)+(2*2)+(1*2)=60
60 % 10 = 0
So 121133-22-0 is a valid CAS Registry Number.

121133-22-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenyl-1-pyridin-3-ylethanimine

1.2 Other means of identification

Product number -
Other names Benzenamine,N-[1-(3-pyridinyl)ethylidene]

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:121133-22-0 SDS

121133-22-0Relevant articles and documents

Thiolate-Protected Au 25 (SC 2 H 4 Ph) 18 Nanoclusters as a Catalyst for Intermolecular Hydroamination of Terminal Alkynes

Nagata, Tatsuki,Adachi, Yurina,Obora, Yasushi

, p. 2655 - 2659 (2018)

Au 25 (SC 2 H 4 Ph) 18 nanoclusters have high catalytic activity for hydroamination of terminal alkynes. This reaction proceeds under O 2 or air. The presence of molecular oxygen has a profound effect

Linear free-energy relationships applied to the 13C NMR chemical shifts in 4-substituted N-[1-(pyridine-3- and -4-yl)ethylidene]anilines

Ran?ic, Milica,Tri?ovic, Nemanja,Mil?ic, Milo?,Jovanovic, Maja,Jovanovic, Bratislav,Marinkovic, Aleksandar

, p. 1442 - 1451 (2015/04/27)

Two series of 4-substituted N-[1-(pyridine-3- and -4-yl)ethylidene]anilines have been synthesized using different methods of conventional and microwave-assisted synthesis, and linear free-energy relationships have been applied to the 13C NMR chemical shifts of the carbon atoms of interest. The substituent-induced chemical shifts have been analyzed using single substituent parameter and dual substituent parameter methods. The presented correlations describe satisfactorily the field and resonance substituent effects having similar contributions for C1 and the azomethine carbon, with exception of the carbon atom in para position to the substituent X. In both series, negative ρ values have been found for C1' atom (reverse substituent effect). Quantum chemical calculations of the optimized geometries at MP2/6-31G++(d,p) level, together with 13C NMR chemical shifts, give a better insight into the influence of the molecular conformation on the transmission of electronic substituent effects. The comparison of correlation results for different series of imines with phenyl, 4-nitrophenyl, 2-pyridyl, 3-pyridyl, 4-pyridyl group attached at the azomethine carbon with the results for 4-substituted N-[1-(pyridine-3- and -4-yl)ethylidene]anilines for the same substituent set (X) indicates that a combination of the influences of electronic effects of the substituent X and the π1-unit can be described as a sensitive balance of different resonance structures.

3-arylcarbonyl-1-(C-attached-N-heteryl)-1H-indoles

-

, (2008/06/13)

2-R2 -R4 -substituted-3-R3 -CO-1-[(C-attached-N-herteryl)-(Alk)n ]-1H-indoles useful as analgesic, anti-rheumatic, anti-inflammatory or anti-glaucoma agents.

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