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2-Propyl-quinoline, also known as 2-ethylpropylquinoline, is an organic compound with the molecular formula C13H13N. It is a derivative of quinoline, a heterocyclic aromatic compound with a benzene ring fused to a pyridine ring. 2-Propyl-quinoline is characterized by the presence of a propyl group (a three-carbon alkyl chain) attached to the 2-position of the quinoline nucleus. 2-propyl-quinoline; picrate is often used as a starting material in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical properties. Picrate, on the other hand, is a salt formed from the reaction of picric acid (2,4,6-trinitrophenol) with a base, typically an alkali metal or ammonium. Picrates are known for their explosive properties and were once used in military applications, such as in detonators and boosters. They are also used as analytical reagents for the detection of certain metal ions. The combination of 2-propyl-quinoline and picrate can be used in various chemical analyses and reactions, taking advantage of the unique properties of both compounds.

1613-40-7

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1613-40-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1613-40-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1613-40:
(6*1)+(5*6)+(4*1)+(3*3)+(2*4)+(1*0)=57
57 % 10 = 7
So 1613-40-7 is a valid CAS Registry Number.

1613-40-7Downstream Products

1613-40-7Relevant academic research and scientific papers

Studies on Tertiary Amine Oxides. LXXV. Reactions of Aromatic N-oxides with Meldrum's Acid in the Presence of Acetic Anhydride

Yousif, Mohammed Mohammed,Saeki, Seitaro,Hamana, Masatomo

, p. 1680 - 1691 (2007/10/02)

Reactions of quinoline, lepidine, 4-chloro-, 4-methoxy- and 4-morpholino-quinoline 1-oxides (1a-e) with Meldrum's acid (2) in acetic anhydride smoothly occurred at room temperature to afford the corresponding 5-(2-quinolyl)-Meldrum's acids (3a-e) in good yields.On the other hand, when the reactions were carried out in dimethylformamide containing 1.2 eq acetic anhydride the N-ylides (4a-e) were produced; while the reactions of 1a, d, e yielded only N-ylides 4a, d, e, 4b, c were formed along with smaller amounts of 3b, c in the reactions of 1b, c. 3-Bromoquinoline 1-oxide (1f) gave only the N-ylide (4f) and isoquinoline 2-oxide (6) gave the 1-substituted isoquinoline (7) independently of the reaction conditions.Further, 5-alkyl-Meldrum's acids (8a-c) also reacted readily with 1a in acetic anhydride to give the corresponding 2-substituted quinolines (9a-c) in good yields.Heating of 3a, b with conc. hydrochloric acid, 10percent hydrochloric acid or methanol containing 10percent hydrogen chloride gave 2-methylquinolines (10a, b), 2-quinolineacetic acids (11a, b) or their methyl esters (12a, b), respectively.Similarly, 9a-c afforded 2-alkylquinolines (14a-c) in good yields upon being refluxed with conc. hydrochloric acid.Keywords--aromatic N-oxide; Meldrum's acid; 5-(2-quinolyl)-Meldrum's acid; quinolinium-5-Meldrum's acid ylide; 5-(1-isoquinolyl)-Meldrum's acid; 2-alkylquinoline; 2-quinolineacetic acid; nucleophilic reaction; regioselectivity

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