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3-(4-chlorobenzyloxy)-3-penten-2-one is an organic compound with the molecular formula C12H13ClO2. It is a colorless to pale yellow liquid with a molecular weight of 224.68 g/mol. This chemical features a 3-penten-2-one core structure, which is a five-carbon unsaturated ketone, with a 4-chlorobenzyloxy group attached to the third carbon. The 4-chlorobenzyloxy group consists of a benzyloxy (C6H5CH2O) moiety with a chlorine atom at the para position of the benzene ring. 3-(4-chlorobenzyloxy)-3-penten-2-one is synthesized through various chemical reactions and is used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and reactivity make it a valuable building block in organic synthesis.

3602-62-8

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3602-62-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3602-62-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,0 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3602-62:
(6*3)+(5*6)+(4*0)+(3*2)+(2*6)+(1*2)=68
68 % 10 = 8
So 3602-62-8 is a valid CAS Registry Number.

3602-62-8Downstream Products

3602-62-8Relevant academic research and scientific papers

C-ALKYLATION OF β-DIKETONES WITH BENZYLPYRIDINIUM SALTS. EVIDENCE FOR CHAIN RADICAL MECHANISMS

Marquet, Jorge,Moreno-Manas, Marcial,Pacheco, Pedro,Prat, Maria,Katritzky, Alan R.,Brycki, Bogumil

, p. 5333 - 5346 (2007/10/02)

1-(p-Substituted benzyl)-2,4,6-triphenylpyridinium cations react with β-diketone anions by mechanisms which depend on the para-substituent.The p-methoxybenzyl derivative undergoes SN1 displacement yielding O- and C-benzylated products.The p-nitrobenzyl compound reacts by a chain radicaloid mechanism and gives high yields of C-p-nitrobenzylated diketones.The parent benzyl compound forms some C- and some O-benzylated products, together with bibenzyl, probably by a radical chain reaction which was suppressed by radical traps.

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