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5-Isopropyl-indan-1-one is an organic compound with the molecular formula C11H14O. It is a derivative of indan-1-one, featuring an isopropyl group (a three-carbon alkyl group) attached to the 5th carbon position of the indan ring. This ketone is known for its unique chemical structure and properties, which can be utilized in various chemical reactions and synthesis processes. It is an important intermediate in the production of pharmaceuticals, fragrances, and other specialty chemicals. The compound is characterized by its distinct chemical reactivity, which can be attributed to the presence of the ketone functional group and the isopropyl substituent.

5120-34-3

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5120-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5120-34-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,2 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5120-34:
(6*5)+(5*1)+(4*2)+(3*0)+(2*3)+(1*4)=53
53 % 10 = 3
So 5120-34-3 is a valid CAS Registry Number.

5120-34-3Relevant academic research and scientific papers

SCHWEFELVERBINDUNGEN DES ERDOELS XXII. ALKYL-10,11-DIHYDRODIINDENOTHIOPHENE

Boberg, Friedrich,Deters, Karin,Schulz, Juergen,Torges, Karl-Franz

, p. 69 - 80 (2007/10/03)

The one-pot syntheses of alkyl-10,11-dihydrodiindenothiophenes (3) by bromination and sulfurization of alkylindan-1-ones without substituents at C-2 (1) has been studied with 14 1 with C1-C4-rests at the benzene and or the cyclopentane ring. 9 dialkyl-3 and 3 tetraalkyl-3 are prepared in yields of 7-66percent; an octamethyl-3 is detected by tlc and ms. 2 dialkyl-3 are prepared too by an independent syntheses from dimethyl 2,5-bis(methylphenyl)thiophene-3,4-dicarboxylates (13).The mechanism of the one-pot syntheses, which gives diindeno-1,4-dithiines too,is discussed.The oxidation of 4 3 has been studied.Key words: Alkylindan-1-ones, alkyl-10,11-dihydrodiindenothiophenes, alkyldiindeno-1,4-dithiines, one-pot syntheses of anellated thiophenes, oxidation of anellated thiophenes.

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