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3-Pyridinecarboxamide, N-(1-phenylethyl)-, also known as N-(1-phenylethyl)nicotinamide or phenethylnicotinamide, is a chemical compound with the molecular formula C12H12N2O. It is a derivative of nicotinamide, which is a form of vitamin B3. 3-Pyridinecarboxamide, N-(1-phenylethyl)- is characterized by a pyridine ring attached to a carboxamide group and a phenylethyl side chain. It is used in various applications, including as a pharmaceutical intermediate and in the synthesis of certain drugs. The compound is known for its potential neuroprotective properties and has been studied for its effects on cognitive function and memory. It is also used in the development of compounds targeting the nicotinic acetylcholine receptor, which plays a crucial role in the nervous system.

2909-33-3

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2909-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2909-33-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,0 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2909-33:
(6*2)+(5*9)+(4*0)+(3*9)+(2*3)+(1*3)=93
93 % 10 = 3
So 2909-33-3 is a valid CAS Registry Number.

2909-33-3SDS

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 N-(1-phenylethyl)nicotinamide

1.2 Other means of identification

Product number -
Other names -

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:2909-33-3 SDS

2909-33-3Downstream Products

2909-33-3Relevant academic research and scientific papers

One-Pot Synthesis of α-Branched N-Acylamines via Titanium-Mediated Condensation of Amides, Aldehydes, and Organometallics

Dai, Chunhui,Genovino, Julien,Bechle, Bruce M.,Corbett, Matthew S.,Huh, Chan Woo,Rose, Colin R.,Sun, Jianmin,Warmus, Joseph S.,Blakemore, David C.

, p. 1064 - 1067 (2017)

A three-component, titanium-mediated synthesis of α-branched N-acylamines from commercial or readily accessible amides, aldehydes, and organometallic reagents is reported. The transformation proceeds under mild reaction conditions and tolerates a variety of functional groups (including nitrile, carbamate, olefin, basic amine, furan, and other sensitive heteroaromatics) to generate a large umbrella of α-branched N-acylamine products in high yields. The operationally practical procedure enables the use of this method in parallel chemical synthesis, a valuable feature that can facilitate the screening of bioactive molecules by medicinal chemists.

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