122-94-1

Basic information

• Product Name: 4-Butoxyphenol
• Synonyms: 4-butoxy-pheno;Phenol, 4-butoxy-;Phenol, p-butoxy-;P-BUTOXYPHENOL;HYDROQUINONE MONOBUTYL ETHER;HYDROQUINONE MONO-N-BUTYL ETHER;4-NORMAL-BUTOXYPHENOL;4-N-BUTOXYPHENOL
• CAS NO: 122-94-1
• Molecular Formula: C₁₀H₁₄O₂
• Molecular Weight: 166.22
• EINECS: 204-583-4
• Product Categories: Aromatic Hydrocarbons (substituted) & Derivatives;Aromatic Phenols;Building Blocks for Liquid Crystals;Functional Materials;Phenols (Building Blocks for Liquid Crystals);Organic Building Blocks;Oxygen Compounds;Phenols;Aromatics;Impurities;Building Blocks;C9 to C20+;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;Aromatics, Impurities
• Mol File: 122-94-1.mol
• Article Data: 33

Chemical Properties

• Melting Point: 65-66 °C(lit.)
• Boiling Point: 165 °C / 2mmHg
• Flash Point: 132.369 °C
• Appearance: Pale brown to brown crystalline powder
• Density: 1.0060 (rough estimate)
• Vapor Pressure: 9.14mmHg at 25°C
• Refractive Index: 1.5200 (estimate)
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility: Soluble in acetone and ethanol.
• PKA: 10.33±0.15(Predicted)
• CAS DataBase Reference: 4-Butoxyphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Butoxyphenol(122-94-1)
• EPA Substance Registry System: 4-Butoxyphenol(122-94-1)

Safety Data

• Hazard Codes: Xn,Xi,T
• Statements: 22-37/38-40-41-43-52/53-42/43-36/37/38-23/24/25-45-R42/43-R36/37/38-R23/24/25-R45
• Safety Statements: 26-36/37/39-61-53-45-22-S53-S45-S36/37/39-S26-S22-37/39
• RIDADR: 2811
• WGK Germany: 3
• TSCA: Yes
• Hazardous Substances Data: 122-94-1(Hazardous Substances Data)

Usage

Chemical Properties

PALE BROWN TO BROWN CRYSTALLINE POWDER

Uses

Different sources of media describe the Uses of 122-94-1 differently. You can refer to the following data:
1. Pramoxine impurity. Phenol derivatives induced tumor cell apoptosis.
2. It is an intermediate of liquid crystals.
3. Intermediates of Liquid Crystals

InChI:InChI=1/C6H11ClO/c1-6(2,3)4-5(7)8/h4H2,1-3H3

Upstream product

• 1126-79-0 n-butyl phenyl ether 
• 53936-56-4 4-(tetrahydro-2H-2-pyranyloxy)phenol 
• 106-41-2 4-bromo-phenol 
• 71-36-3 butan-1-ol 
• 20743-95-7 1-butoxy-4-methoxybenzene 
• 96693-04-8 1-(n-butoxy)-4-iodobenzene 
• 105365-51-3 4-butoxyphenylboronic acid 
• 103-16-2 4-Benzyloxyphenol 
• 123-31-9 hydroquinone 
• 106-51-4 p-benzoquinone 
• 2444-82-8 Butyl-aluminium-dichlorid 
• 109-65-9 1-bromo-butane 
• 25079-10-1 dibutoxy(tert-butyldioxy)borane 
• 542-69-8 1-iodo-butane 

Downstream Products

• 18110-27-5 (4-butoxy-phenoxymethyl)-oxirane 
• 100840-47-9 2-[3-(4-Butoxy-phenoxy)-propyl]-isoindole-1,3-dione 
• 38559-81-8 2-(4-butoxyphenoxy)acetic acid 
• 67590-12-9 trans-4-n-Butyloxycyclohexanol 
• 52267-53-5 4-n-Octyloxy-benzoesaeure<4-n-butoxy-phenylester> 
• 93408-25-4 4-Butyloxy-2-(3,4-dichlor-benzyl)-phenol 
• 134254-33-4 3-(4-butoxyphenoxy)propane-1,2-diol 
• 104-36-9 1,4-dibutoxybenzene 
• 142860-21-7 2-Allyl-4-butoxy-phenol 
• 958401-66-6 (1-(allyloxy)-4-butoxybenzene) 

Relevant articles and documents

Synthesis of 4-[(1R,4R)-3-oxo-p-menthan-2-ylidenemethyl]benzoic acid and its esters

Carbonylation of (E)-2-(4-halobenzylidene)-p-menthan-3-ones, catalyzed by PdCl2(PPh3)2, gave a distereometric mixure of 4-[(1R,4R)- and (1R,4S)-3-oxo-p-menthan-2-ylidenemethyl]benzoic acids, whose reaction with phenols gave 1R,4R diastereomers of the corresponding esters. 2005 Pleiades Publishing, Inc.

Para -Selective hydroxylation of alkyl aryl ethers

para-Selective hydroxylation of alkyl aryl ethers is established, which proceeds with a ruthenium(ii) catalyst, hypervalent iodine(iii) and trifluoroacetic anhydride via a radical mechanism. This protocol tolerates a wide scope of substrates and provides a facile and efficient method for preparing clinical drugs monobenzone and pramocaine on a gram scale.

Tetracyano-anthraquinone dimethane micromolecular receptor material as well as preparation method and application thereof

The invention relates to a tetracyano-anthraquinone dimethane micromolecular acceptor material as well as a preparation method and application thereof. The structure of the acceptor material is as shown in a formula I, which is described in the specification. The micromolecular acceptor material has good solubility and stability, the absorption spectrum is well matched with the solar spectrum, andthe micromolecular acceptor material can be used for organic solar cells.