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[4-nitro-3-(nitromethyl)butyl]benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

757237-59-5

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757237-59-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 757237-59-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,7,2,3 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 757237-59:
(8*7)+(7*5)+(6*7)+(5*2)+(4*3)+(3*7)+(2*5)+(1*9)=195
195 % 10 = 5
So 757237-59-5 is a valid CAS Registry Number.

757237-59-5Relevant academic research and scientific papers

Highly efficient C-C bond-forming reactions in aqueous media catalyzed by monomeric vanadate species in an apatite framework

Hara, Takayoshi,Kanai, Satoko,Mori, Kohsuke,Mizugaki, Tomoo,Ebitani, Kohki,Jitsukawa, Koichiro,Kaneda, Kiyotomi

, p. 7455 - 7462 (2007/10/03)

A calcium vanadate apatite (VAp), in which PO43- of hydroxyapatite (HAP), Ca10(PO4)6(OH) 2, is completely substituted by VO43- in the apatite framework, was synthesized. Physicochemical analysis of the VAp reveals the presence of isolated VO4 tetrahedron units with a pentavalent oxidation state. The VAp acts as a high-performance heterogeneous base catalyst for various carbon-carbon bond-forming reactions such as Michael and aldol reactions in aqueous media and the H-D exchange reactions using deuterium oxide. For example, a 200-mmol-scale Michael reaction under triphasic conditions proceeded rapidly, with an extremely high turnover number of up to 260 400 and an excellent turnover frequency of 48 s-1. No vanadium leaching was detected during the above reactions, and the catalyst was readily recycled with no loss of activity.

One-pot synthesis of 1,3-dinitroalkanes under heterogeneous catalysis

Ballini, Roberto,Bosica, Giovanna,Fiorini, Dennis,Palmieri, Alessandro

, p. 1938 - 1940 (2007/10/03)

Reaction of aldehydes with an excess of nitromethane in the presence of basic alumina as solid catalyst allows the one pot preparation of 1,3-dinitroalkanes. The synthesis proceeds through the nitroaldol reaction of nitromethane, which acts both as nucleo

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