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3-morpholin-4-yl-1-thiophen-2-ylpropan-1-one is a complex organic compound with the molecular formula C12H15NO2S2. It features a thiophene ring, which is a five-membered aromatic ring with one sulfur atom, and a morpholine ring, which is a five-membered cyclic ether. The compound has a propanoic acid side chain with a ketone group at the end, and the morpholine ring is attached to the third carbon of the propanoic acid chain. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through multi-step organic reactions and is used as an intermediate in the preparation of more complex molecules.

3339-36-4

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3339-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3339-36-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,3 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3339-36:
(6*3)+(5*3)+(4*3)+(3*9)+(2*3)+(1*6)=84
84 % 10 = 4
So 3339-36-4 is a valid CAS Registry Number.

3339-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-Morpholinyl)-1-(2-thienyl)-1-propanone

1.2 Other means of identification

Product number -
Other names 3-morpholino-1,2,5-thiadiazole

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:3339-36-4 SDS

3339-36-4Relevant academic research and scientific papers

PEG 400/cerium ammonium nitrate combined with microwave-assisted synthesis for rapid access to beta-amino ketones. an easy-to-use protocol for discovering new hit compounds

Rossino, Giacomo,Raimondi, Maria Valeria,Rui, Marta,Di Giacomo, Marcello,Rossi, Daniela,Collina, Simona

, (2018/04/06)

Compound libraries are important requirement in target-based drug discovery. In the present work, a small focused compound library based on β-aminoketone scaffold has been prepared combining microwave-assisted organic synthesis (MAOS) with polymer-assiste

Synthesis of some new thienyl and 1,3-thiazolyl-aminoketones with anti- inflammatory activity

Geronikaki, Athina A.,Hadjipavlou-Litina, Dimitra J.,Tzaki, Maria

, p. 266 - 271 (2007/10/03)

Eight thienyl and 1,3-thiazolyl-aminoketones were synthesised and tested as anti-inflammatory agents, pKa and log P were theoretically calculated. The compounds were tested for antioxidant activity, as hydroxyl radical scavengers, as superoxide anion scavengers and for their ability to interact with 1,1-diphenyl-2-picryl hydrazyl stable free radical (DPPH. The effects of the synthesised compounds on inflammation were studied using the carrageenan induced mice paw oedema model. Both anti-inflammatory and antioxidant activities depended on some structural characteristics of the synthesised compounds.

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