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Anthracene, 9-propyl-, also known as 9-propylanthracene, is an organic compound with the chemical formula C17H14. It is a derivative of anthracene, a tricyclic aromatic hydrocarbon consisting of three fused benzene rings. The propyl group (a three-carbon alkyl chain) is attached to the 9th carbon atom of the anthracene molecule. Anthracene, 9-propyl- is a white crystalline solid with a melting point of approximately 70°C. 9-Propylanthracene is used as a precursor in the synthesis of various organic compounds, particularly in the production of dyes and pharmaceuticals. It is also employed as a research chemical and a reagent in various chemical reactions. Due to its potential environmental and health risks, handling and disposal of 9-propylanthracene should be done with proper safety measures and in accordance with local regulations.

1498-77-7

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1498-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1498-77-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,9 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1498-77:
(6*1)+(5*4)+(4*9)+(3*8)+(2*7)+(1*7)=107
107 % 10 = 7
So 1498-77-7 is a valid CAS Registry Number.

1498-77-7Downstream Products

1498-77-7Relevant academic research and scientific papers

Palladium-catalysed direct cross-coupling of secondary alkyllithium reagents

Vila, Carlos,Giannerini, Massimo,Hornillos, Valentin,Fananas-Mastral, Martin,Feringa, Ben L.

, p. 1361 - 1367 (2014/03/21)

Palladium-catalysed cross-coupling of secondary C(sp3) organometallic reagents has been a long-standing challenge in organic synthesis, due to the problems associated with undesired isomerisation or the formation of reduction products. Based on our recently developed catalytic C-C bond formation with organolithium reagents, herein we present a Pd-catalysed cross-coupling of secondary alkyllithium reagents with aryl and alkenyl bromides. The reaction proceeds at room temperature and on short timescales with high selectivity and yields. This methodology is also applicable to hindered aryl bromides, which are a major challenge in the field of metal catalysed cross-coupling reactions.

An easy synthesis of lepidopterene from 9-chloromethyl anthracene. Evidence for a free radical mechanism

Fernández, María-José,Gude, Lourdes,Lorente, Antonio

, p. 891 - 893 (2007/10/03)

This communication reports a novel and efficient synthesis of lepidopterene from 9-(chloromethyl)anthracene. Furthermore, the radical nature of the process is unambiguously established through the obtention of several 9-anthracenemethyl derivatives, which are formed via a common 9-anthracenemethyl radical intermediate, derived from 9-(iodomethyl)anthracene.

Reduction of Polycyclic Arenes by BH Boranes, III. Partial Hydrogenation: From Anthracene to Coronene

Yalpani, Mohamed,Koester, Roland

, p. 719 - 724 (2007/10/02)

Tetrapropyldiboran(6) (TPDB) katalysiert die Hydrierung polycyclischer Arene unter Wasserstoff-Druck bei bei 200 deg C.In einigen Faellen koennen sehr hohe Ausbeuten an Hydroarenen erzielt werden .Neben unterschiedlichen kleinen Mengen an Perhydroarenen bilden sich nach langer Reaktionszeit aus saemtlichen Arenen auch C-C-Spaltungsprodukte.

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