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1,1-bis(methoxycarbonyl)-3-methoxy-3-phenylpropane is a complex organic compound with the molecular formula C14H18O6. It is characterized by a propane backbone, with two methoxycarbonyl groups attached to the terminal carbon atoms (1-position) and a methoxy group attached to the central carbon atom (3-position). Additionally, a phenyl ring is attached to the same central carbon atom, which contributes to the compound's structure and properties. This chemical is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. Its stability and versatility make it a valuable intermediate in organic chemistry, particularly in the preparation of complex molecules that require a propane scaffold with multiple functional groups.

3709-35-1

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3709-35-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3709-35-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,0 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3709-35:
(6*3)+(5*7)+(4*0)+(3*9)+(2*3)+(1*5)=91
91 % 10 = 1
So 3709-35-1 is a valid CAS Registry Number.

3709-35-1Relevant academic research and scientific papers

New dimerization and cascade oligomerization reactions of dimethyl 2-phenylcyclopropan-1,1-dicarboxylate catalyzed by Lewis acids

Novikov, Roman A.,Korolev, Victor A.,Timofeev, Vladimir P.,Tomilov, Yury V.

scheme or table, p. 4996 - 4999 (2011/10/08)

New routes to transform donor-acceptor cyclopropanes in the presence of Lewis acids have been found. The reaction of dimethyl 2-phenylcyclopropan-1,1- dicarboxylate, a typical representative of this class of compounds, with an equimolar amount of anhydrou

Oxidative addition of dimethyl malonate to styrenes mediated by cerium(IV) ammonium nitrate: Some novel observations

Nair, Vijay,Mathew, Jessy,Nair, Latha G.

, p. 3053 - 3064 (2007/10/03)

The oxidative addition of dimethyl malonate to ring substituted styrenes leads to the formation of substituted dimethyl (2-oxo-2-phenylethyl) malonate and methyl 2-oxo-5-phenyltetrahydrofuran-3-carboxylate along with small amounts of substituted dimethyl [2-(nitrooxy)-2-phenylethyl] malonate and dimethyl 2-methoxy-2-phenylethyl) malonate. A tentative mechanism which supports the formation of these products is also presented.

Cerium(IV) ammonium nitrate mediated addition of dimethyl malonate to styrene: a remarkable reaction

Nair, Vijar,Jessy, Methew

, p. 1881 - 1882 (2007/10/02)

Cerium(IV) ammonium nitrate mediated addition of dimethyl malonate to styrene afforded the products 3 and 4 (via 7) along with small amounts of 5 and 6.

Relative Rates for the Addition Reactions of the Malonyl Radical to Substituted Styrenes Induced by Cerium(IV) Ammonium Nitrate and Tributyltin Hydride. A Comparison

Baciocchi, Enrico,Giese, Bernd,Farshchi, Hassan,Ruzziconi, Renzo

, p. 5688 - 5691 (2007/10/02)

The relative rates for the addition reactions of the malonyl radical to substituted styrenes induced by cerium(IV) ammonium nitrate (CAN) and tributyltin hydride have been determined.The two processes exhibit practically identical ρ+ values (-1.05 and -1.06), thus suggesting that the coordination between the metal and the radical does not play a significant role in the CAN-promoted oxidative additions.

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