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3-Hexyl nitrate, also known as 1-hexanol, 2-nitro-, is an organic compound with the chemical formula C6H13ONO2. It is a nitrate ester derived from 1-hexanol, where a hydroxyl group is replaced by a nitrate group. This colorless liquid is used as a plasticizer, a substance added to plastics to increase their flexibility and workability. 3-Hexyl nitrate is also employed as a solvent and a component in the production of various chemicals. It is important to note that, like other nitrate esters, 3-hexyl nitrate can be hazardous and should be handled with care due to its potential to decompose and release toxic gases.

7286-40-0

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7286-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7286-40-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,8 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7286-40:
(6*7)+(5*2)+(4*8)+(3*6)+(2*4)+(1*0)=110
110 % 10 = 0
So 7286-40-0 is a valid CAS Registry Number.

7286-40-0Upstream product

7286-40-0Downstream Products

7286-40-0Relevant academic research and scientific papers

A simple and efficient approach for highly selective preparation of nitrocyclohexane from cyclohexane with tert-butyl nitrite catalyzed by N-hydroxyphthalimide

Liu, Shuilin,You, Kuiyi,Jian, Jian,Luo, Qing,Liu, Pingle,Ai, Qiuhong,Luo, He'An

, p. 2211 - 2220 (2016)

A simple and effective approach for highly selective preparation of nitrocyclohexane from cyclohexane using tert-butyl nitrite as a nitrating agent under atmospheric pressure has been successfully developed in this work. The results indicate that the N-hydroxyphthalimide catalyst gave the best results with 27.3 % of cyclohexane conversion and 88.0 % of selectivity to nitrocyclohexane under optimal reaction conditions. The present reaction provides a novel strategy for the synthesis of nitroalkanes from the nitration of low-carbon alkanes because of the mild reaction condition, simple experimental procedure and high selectivity towards the desired product. This method may be very significant to establish such a synthesis method for aliphatic nitro-compounds from the low-carbon alkanes in organic fields.

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