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(1-Nitrocyclohexyl)methanol is an organic compound with the molecular formula C7H13NO3. It is a derivative of cyclohexanol, where one of the hydrogen atoms on the cyclohexane ring is replaced by a nitro group (-NO2) and a hydroxymethyl group (-CH2OH). (1-nitrocyclohexyl)methanol is characterized by its nitro functional group, which imparts explosive properties, and its hydroxymethyl group, which provides reactivity for further chemical transformations. It is a colorless to pale yellow liquid with a pungent odor and is used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential hazards, it is important to handle (1-nitrocyclohexyl)methanol with care and in accordance with proper safety protocols.

3719-52-6

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3719-52-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3719-52-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,1 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3719-52:
(6*3)+(5*7)+(4*1)+(3*9)+(2*5)+(1*2)=96
96 % 10 = 6
So 3719-52-6 is a valid CAS Registry Number.

3719-52-6Relevant academic research and scientific papers

Preparation of indium nitronates and their Henry reactions

Soengas, Raquel G.,Acrcio, Rita,Silva, Artur M. S.

, p. 8593 - 8597 (2014)

Indium nitronates were readily prepared from commercially available nitroalkanes by transmetallation of the corresponding lithium nitronates with indium salts. The Henry reaction of this indium organometallics with aldehydes afforded β-nitroalkanols in moderate to high yields. The use of chiral sugar aldehydes furnished the corresponding carbohydrate-derived β-nitroalkanols with excellent stereoselectivity.

Convenient procedure for the indium-mediated hydroxymethylation of active bromo compounds: Transformation of ketones into α-hydroxymethyl nitroalkanes

Soengas, Raquel G.,Estévez, Amalia M.

, p. 2625 - 2627 (2010)

A very simple, safe and powerful method for the hydroxymethylation of 2-bromoesters and lactones under anhydrous conditions that avoids the use of gaseous formaldehyde is described. Moreover, under these conditions, bromonitroalkanes were converted into the corresponding α- monohydroxymethylated nitroalkanes, which are precursors of the corresponding α-amino acids. Considering the easy transformation of ketones into bromonitroalkanes, this represents a method for the formal synthesis of α-amino acids from ketones. Georg Thieme Verlag Stuttgart New York.

PROCESS FOR MAKING TERTIARY AMINOALCOHOL COMPOUNDS

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Page/Page column 13, (2012/04/17)

Provided is a process for making a tertiary aminoalcohol compound. The process comprises using an excess amount of a carbonyl compound in a condensation step between the carbonyl compound and a nitroalkane, and conducting a hydrogenation/alkylation step to produce the tertiary aminoalcohol. The process uses fewer steps than conventional processes.

AMINOALCOHOL AND BIOCIDE COMPOSITIONS FOR AQUEOUS BASED SYSTEMS

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Page/Page column 13-14, (2009/12/23)

Biocidal compositions and their use in aqueous media, such as metalworking fluids, the compositions comprising a biocidal agent; and a non-biocidal primary amino alcohol compound of the formula (I): wherein R1, R2, R3, R4, and R5 are as defined herein.

IMPROVED CORROSION AND MICROBIAL CONTROL IN HYDROCARBONACEOUS COMPOSITIONS

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Page/Page column 15-16, (2009/12/23)

Provided are additives of formula I for use in hydrocarbonaceous compositions, such as petroleum or liquid fuels: (I) wherein R1, R2, R3, R4, and R5 are as defined herein. The additives improve the corrosion resistance of the compositions. The additives a

NITRATED HYDROCARBONS, DERIVATIVES, AND PROCESSES FOR THEIR MANUFACTURE

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Page/Page column 35, (2009/12/02)

Provided is a process for the formation of nitrated compounds by the nitration of hydrocarbon compounds with dilute nitric acid. Also provided are processes for preparing industrially useful downstream derivatives of the nitrated compounds, as well as novel nitrated compounds and derivatives, and methods of using the derivatives in various applications.

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