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(E)-1-(cyclohex-1-en-1-yl)-N-hydroxymethanimine is a chemical compound characterized by the molecular formula C7H11NO. It is a hydroxylamine derivative featuring a cyclohexene group attached to a hydroxymethanimine functional group. (E)-1-(cyclohex-1-en-1-yl)-N-hydroxymethanimine holds potential in various fields, including organic synthesis and pharmaceutical and medicinal chemistry, due to its intriguing biological activity. However, it is crucial to handle and store (E)-1-(cyclohex-1-en-1-yl)-N-hydroxymethanimine with caution, as it may pose hazards if not used properly. Further research and experimentation are essential to fully comprehend its properties and potential applications.

30950-32-4

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30950-32-4 Usage

Uses

Used in Organic Synthesis:
(E)-1-(cyclohex-1-en-1-yl)-N-hydroxymethanimine is utilized as a reagent in organic synthesis, contributing to the creation of various complex organic molecules. Its unique structure allows for versatile reactions and the formation of a wide range of products, making it a valuable component in this field.
Used in Pharmaceutical and Medicinal Chemistry:
In the pharmaceutical and medicinal chemistry industry, (E)-1-(cyclohex-1-en-1-yl)-N-hydroxymethanimine is of interest due to its potential biological activity. Researchers are exploring its possible applications in the development of new drugs and therapeutic agents, capitalizing on its unique chemical properties to target specific biological processes and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 30950-32-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,9,5 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 30950-32:
(7*3)+(6*0)+(5*9)+(4*5)+(3*0)+(2*3)+(1*2)=94
94 % 10 = 4
So 30950-32-4 is a valid CAS Registry Number.

30950-32-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (NE)-N-(cyclohexen-1-ylmethylidene)hydroxylamine

1.2 Other means of identification

Product number -
Other names 1-cyclohexene aldoxime

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:30950-32-4 SDS

30950-32-4Downstream Products

30950-32-4Relevant academic research and scientific papers

Grignard reaction of substituted nitromethanes: The nwe observations

Gupta, Ramesh Chandra,Seth, M,Bhaduri, A P

, p. 745 - 747 (2007/10/02)

Reactions of 1-(1-nitromethyl)cyclohexene and its derivatives with excess of methylmagnesium iodide have been studied.In a few cases a chemoselective attack on the nitro group by the Grignard reagent has been observed.The N,N-dialkylhydroxylamine, the nor

Reduction of Allylic Nitro Compounds to Oximes with Carbon Disulfide under Solid-Liquid Phase-Transfer Catalysis Conditions

Albanese, Domenico,Landini, Dario,Penso, Michele

, p. 333 - 336 (2007/10/02)

A mild procedure for the synthesis of allylic oximes 2 from the corresponding nitro derivatives 1, using carbon disulfide as reducting agent in the presence of wet potassium carbonate and a catalytic amount of a phase-transfer agent, is described.

One-pot Conversion of Allylic Nitro Compounds Into Nitriles with Carbon Disulphide under Phase-transfer Catalysis Conditions

Albanese, Domenico,Landini, Dario,Penso, Michele,Pozzi, Gianluca

, p. 965 - 971 (2007/10/02)

An one-pot synthesis of allylic nitriles 3 from the corresponding nitro derivatives 1 is described.In the first step the substrates 1 are reduced to the oximes 2 by carbon disulphide in the presence of wet potassium carbonate, in solid-liquid PTC conditions.In the second, the formed oximes 2 are dehydrated by adding more CS2 and 15percent aqueous NaOH.

Photochemical Conversion of Aliphatic Nitro Compounds into Oximes

Takechi, Haruko,Machida, Minoru

, p. 206 - 207 (2007/10/02)

Aliphatic nitro compounds are converted into oximes by irradiation in acetone in the presence of triethylamine in moderate yields.

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