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4-(Hexan-3-yl)phenol is an organic compound with the molecular formula C12H18O. It is a derivative of phenol, where a hexan-3-yl group (a six-carbon alkyl chain with a methyl group on the third carbon) is attached to the para position (4-position) of the phenol ring. 4-(hexan-3-yl)phenol is characterized by its aromatic ring structure and a long alkyl chain, which can influence its physical properties such as solubility and boiling point. It is a colorless to pale yellow liquid with a distinct phenolic odor. 4-(Hexan-3-yl)phenol is used in various applications, including as a chemical intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure also makes it a potential candidate for research in materials science and organic chemistry.

6925-42-4

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6925-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6925-42-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,2 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6925-42:
(6*6)+(5*9)+(4*2)+(3*5)+(2*4)+(1*2)=114
114 % 10 = 4
So 6925-42-4 is a valid CAS Registry Number.

6925-42-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hexan-3-ylphenol

1.2 Other means of identification

Product number -
Other names 3-<4-Hydroxy-phenyl>-hexan

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:6925-42-4 SDS

6925-42-4Relevant academic research and scientific papers

Highly selective aromatic alkylation of phenol and anisole by using recyclable bronsted acidic ionic liquid systems

Titze-Frech, Karin,Ignatiev, Nikolai,Uerdingen, Marc,Schulz, Peter Steffen,Wasserscheid, Peter

, p. 6961 - 6966 (2013/11/06)

A highly efficient ionic liquid catalyst system for selective alkylation of phenol and anisole with alkenes is described. By using Bronsted acidic triflate ionic liquids containing the SO3H group attached to the cation, it was possible to recycle the catalyst and reuse it after a simple workup procedure. Moreover, selectivity towards the monoalkylated products was improved to 93 % by using a biphasic system. A sulfonic acid functionalized ionic liquid is used as catalyst in the hexylation of phenol and anisol, enabling very high product selectivities, simple product isolation and effective catalyst recycling. The observed selectivity boost is mainly due to differential solubility effects of the liquid-liquid biphasic reaction system established by the ionic liquid catalyst. Copyright

Equilibria for the isomerization of (secondary-alkyl)phenols and cyclohexylphenols

Nesterova, T. N.,Pimerzin, A. A.,Rozhnov, A. M.,Karlina, T. N.

, p. 385 - 396 (2007/10/02)

Equilibria of a series of isomerizations and trans-alkylations of alkylphenols have been investigated in the liquid phase over a wide range of temperatures.Equilibria of isomerizations connected with the displacement of a substituent on a benzene nucleus were studied for secondary-butyl, -amyl, -hexyl, and cyclohexyl-phenols, and di-(secondary-butyl)phenols.Equilibria of positional isomerization connected with the displacement of an oxyphenyl radical in an alkyl chain were investigated for oxyphenyl-pentanes, -hexanes, -octanes, and -decanes.Trans-alkylation was investigated for di- and tri-(secondary-butyl)phenols.Values of ΔrH0m and ΔrS0m were found for all investigated reactions.An analysis was made of the thermodynamic quantities for the reactions.Enthalpies of formation of isopropylphenols (IPP) in the gaseous state were calculated.The values of ΔfH0m/(kJ * mol-1) were found at 298.15 K: o-IPP, -(175.3 +/- 2.4); p-IPP, -(175.3 +/- 2.4); m-IPP, -(175.3 +/-2.4); 2,4-di-IPP, -(254.1 +/- 2.8); 2,5-di-IPP, -(254.1 +/- 2.8); 2,6-di-IPP, -(254.1 +/- 2.8); 3,5-di-IPP, -(254.1 +/- 2.8); 2,4,6-tri-IPP, -(333.0 +/- 3.1).

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