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Benzoic acid, 3,5-dinitro-, cyclohexyl ester is a chemical compound with the molecular formula C14H14N2O6. It is an ester derivative of benzoic acid, featuring a cyclohexyl group attached to the carboxylic acid moiety and two nitro groups (-NO2) at the 3rd and 5th positions on the benzene ring. Benzoic acid, 3,5-dinitro-, cyclohexyl ester is characterized by its yellow crystalline appearance and has a melting point of approximately 68-70°C. It is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential applications, it is essential to handle Benzoic acid, 3,5-dinitro-, cyclohexyl ester with care, following proper safety protocols and guidelines.

1158-19-6

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1158-19-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1158-19-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,5 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1158-19:
(6*1)+(5*1)+(4*5)+(3*8)+(2*1)+(1*9)=66
66 % 10 = 6
So 1158-19-6 is a valid CAS Registry Number.

1158-19-6Relevant academic research and scientific papers

Solid-Phase Benzoylation of Phenols and Alcohols in Microwave Reactor: An Ecofriendly Protocol

Chakraborty, Suchandra,Saha, Ahana,Basu, Kaushik,Saha, Chandan

supporting information, p. 2331 - 2343 (2015/10/12)

An efficient solid-phase benzoylation of phenols and alcohols was developed under microwave irradiation. A stoichiometric amount of benzoyl chloride was sufficient to carry out the reaction. This benzoylation features short reaction time, good yields, and easy workup procedures. Furthermore, the scope of the reaction was extended to prepare 3,5-dinitrobenzoyl derivatives of alcohols.

Heterocycles in organic materials chemistry. Synthesis of di-, tri-, and tetraimide polycarboxylic acids for use in organic network assembly

Feldman, Ken S.,Liu, Yanze,Saunders, Joe C.,Masters, Katherine M.,Campbell, Robert F.

, p. 1527 - 1554 (2007/10/03)

Seven linear divalent monomers, three bent divalent amide-containing monomers, 11 bent divalent ester-containing monomers, one planar trivalent monomer, and two tetrahedral tetravalent monomers were prepared by imide-forming condensation of the appropriat

Esterification of Aromatic Carboxylic Acids with Alcohols Using 2-Chloro-3,5-dinitropyridine as a Condensing Agent

Takimoto, Seiji,Abe, Naomi,Kodera, Yasushi,Ohta, Hiroshi

, p. 639 - 640 (2007/10/02)

The reaction of 2-chloro-3,5-dinitropyridine (CDNP) with carboxylic acids and alcohols was examined, and it was found that CDNP was a useful condensing agent.Various esters were prepared in good yields.

REAGENTS AND SYNTHETIC METHODS 28. MODIFIED PROCEDURES FOR ANHYDRIZATION, ESTERIFICATION AND THIOLESTERIFICATION OF CARBOXYLIC ACIDS BY MEANS OF AVAILABLE PHOSPHORUS REAGENTS.

Arrieta, A.,Garcia, T.,Lago, J. M.,Palomo, C.

, p. 471 - 488 (2007/10/02)

Carboxylic acid anhydrides, esters and thiol esters are obtained by a one-pot method from carboxylic acids and alcohols or thiol by means of phosphorus oxychloride or phenyl dichlorophosphoridate reagents.

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