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2-HYDROXY-4-N-HEXYLOXYBENZOPHENONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

3293-97-8

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3293-97-8 Usage

Preparation

Obtained by reaction of n-hexyl bromide with resbenzo-phenone, ? in the presence of sodium hydroxide in dilute ethanol in a water bath for 18–23 h (15%) ; ? in the presence of potassium carbonate in refluxing acetone for 20 h.

Check Digit Verification of cas no

The CAS Registry Mumber 3293-97-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3293-97:
(6*3)+(5*2)+(4*9)+(3*3)+(2*9)+(1*7)=98
98 % 10 = 8
So 3293-97-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H22O3/c1-2-3-4-8-13-22-16-11-12-17(18(20)14-16)19(21)15-9-6-5-7-10-15/h5-7,9-12,14,20H,2-4,8,13H2,1H3

3293-97-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Hydroxy-4-n-hexyloxy-benzophenon

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-4-hexyloxy-benzophenon

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:3293-97-8 SDS

3293-97-8Downstream Products

3293-97-8Relevant academic research and scientific papers

Synthese von 4-Alkoxy-2-hydroxyphenylketoximen als Metallextraktions-Reagenzien

Beger, J.,Binte, H.-J.,Brunne, L.,Neumann, R.

, p. 269 - 277 (2007/10/02)

The C-Acylation (Friedel-Crafts reaction) of resorcinol with aluminium chloride, the monoetherification in 4-position of the resulting 2,4-dihydroxyphenylketones, and the preparation of oximes (8, 9, 10, 11) from this ketones were investigated.The compounds obtained are characterized by elemental analysis, and the i.r., u.v. and 1H-n.m.r. spectra are discussed.Solubility data of some oximes are determined in water, octane and toluene.The extraction properties for copper-(II)-and iron-(III)-ions are measured by isotope methods in relation to the extragent structure, the extraction time and the pH-range.

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