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1,8-bis(dimethylamino)-2,7-bis(phenylethynyl)-naphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1532528-03-2

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1532528-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1532528-03-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,3,2,5,2 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1532528-03:
(9*1)+(8*5)+(7*3)+(6*2)+(5*5)+(4*2)+(3*8)+(2*0)+(1*3)=142
142 % 10 = 2
So 1532528-03-2 is a valid CAS Registry Number.

1532528-03-2Upstream product

1532528-03-2Downstream Products

1532528-03-2Relevant academic research and scientific papers

Multiple transformations of 2-alkynyl-1,8-bis(dimethylamino)naphthalenes into Benzo[ g ]indoles. Pd/Cu-dependent switching of the electrophilic and nucleophilic sites in acetylenic bond and a puzzle of porcelain catalysis

Filatova, Ekaterina A.,Pozharskii, Alexander F.,Gulevskaya, Anna V.,Ozeryanskii, Valery A.

, p. 872 - 881 (2015)

By means of Sonogashira reaction, a series of 2-alkynyl- and 2,7-dialkynyl derivatives of 1,8-bis(dimethylamino)naphthalene ( proton sponge ) have been obtained from the corresponding iodides. It was disclosed that changing the reaction conditions and isolation protocol or conducting the model experiments with the authentic acetylenes results in several types of palladium- and copper-assisted heterocyclizations with the participation of the C≡C bond and 1-NMe2 group. These include: (i) a cyclization into isomeric 1H-benzo[g]indoles with [1,3] migration of the N-methyl group into the newly formed pyrrole ring; (ii) a similar cyclization with a loss of the methyl group; (iii) a tandem process of cyclization into benzo[g]indoles and their subsequent 3,3′-dimerization; and (iv) a copper-catalyzed oxidative transformation into 3-aroylbenzo[g]indoles. In most cases, the reactions occur in parallel, but under certain conditions, one of the above products becomes predominant or even the only one. Remarkably, in Pd-catalyzed cyclizations i-iii, the acetylenic bond behaves as an electrophile being attacked at the β-position by the amine nitrogen atom. In contrast, in transformation iv, the C≡C bond attacks by its Cα atom on the aminomethyl radical functionality N(Me)-CH2· presumably arising at copper oxidation/deprotonation of the 1-NMe2 group. Studying rearrangement i, some evidence for the porcelain catalysis was obtained.

Synthesis of 2-alkynyl-, 4-alkynyl-, and 2,7-dialkynyl-1,8- bis(dimethylamino)naphthalenes and the unexpected influence of ortho -alkynyl groups on their basicity

Filatova, Ekaterina A.,Pozharskii, Alexander F.,Gulevskaya, Anna V.,Vistorobskii, Nikolay V.,Ozeryanskii, Valery A.

supporting information, p. 2515 - 2518 (2013/12/04)

Novel 2-alkynyl-, 4-alkynyl-, and 2,7-dialkynyl derivatives of 1,8-bis(dimethylamino)naphthalene ('proton sponge') have been synthesized and their basicity values have been measured by competitive NMR studies in DMSO. These indicate that, while the para-alkynyl groups decrease the basicity of the parent proton sponge approximately by one order of magnitude in accordance with their electron-accepting nature, the influence of ortho-alkynyl functionalities is unexpectedly base-enhancing. The latter phenomenon has been ascribed to the appearance of a buttressing effect, but some other factors can be also at work. Georg Thieme Verlag Stuttgart New York.

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