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2-Cyclohexen-1-ol, nitrate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54111-03-4

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54111-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54111-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,1 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54111-03:
(7*5)+(6*4)+(5*1)+(4*1)+(3*1)+(2*0)+(1*3)=74
74 % 10 = 4
So 54111-03-4 is a valid CAS Registry Number.

54111-03-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohex-2-en-1-ol,nitric acid

1.2 Other means of identification

Product number -
Other names 2-Cyclohexen-1-ol,nitrate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:54111-03-4 SDS

54111-03-4Downstream Products

54111-03-4Relevant academic research and scientific papers

A New Synthesis of Allyl Nitrates from Allylmetal (Group IVb) Compounds and Thallium(III) Nitrate

Ochiai, Masahito,Fujita, Eiichi,Arimoto, Masao,Yamaguchi, Hideo

, p. 887 - 890 (2007/10/02)

A new general method for the synthesis of allyl nitrates is described.Allylmetal (group IVb) compounds, on treatment with thallium(III) nitrate in dioxane, gave the corresponding allyl nitrates in good yields.Keywords - allyl nitrate; thallium(III) nitrate; allylsilane; allylgermane; allylstannane; umpolung.

Reaction of Nitrogen Dioxide with Alkenes and Polyunsaturated Fatty Acids: Addition and Hydrogen Abstraction Mechanisms

Pryor, William A.,Lightsey, John W.,Church, Daniel F.

, p. 6685 - 6692 (2007/10/02)

The reactions of nitrogen dioxide in a carrier gas (nitrogen, oxygen, or air) with cyclohexene and a series of mono-, di-, and trienes is reported at NO2 concentrations ranging from 70 ppm to 50percent.A complete product analysis was made with cyclohexene, and these data allow the calculation of the fraction of the NO2 that reacts by addition to the double bond or by abstraction of an allylic hydrogen.At high concentrations of NO2, addition is the predominant process, in agreement with the literature.However, below 10 000 ppm (1percent), hydrogen abstraction predominates.We suggest this is because of competition between a reversible addition and an irreversible H-abstraction step, much as is the case for the well-known bromine atom reaction system.In fact, a kinetic analysis shows that the ratios of rate constants for addition and abstraction are similar for both NO2 and the bromine atom.A less direct method (analysis of water formed) was used to estimate the addition to abstraction ratio for other alkenes and for esters of unsaturated fatty acids; these data are in agreement with the cyclohexene data.The autoxidation of unsaturated fatty acid esters initiated by NO2 also was studied, and kinetic chain lengths and autoxidizability ratios are given.

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