82657-70-3

Basic information

• Product Name: (4-propylphenyl)Methanol
• Synonyms: (4-propylphenyl)Methanol
• CAS NO: 82657-70-3
• Molecular Weight: 150.221
• EINECS: -0
• Mol File: 82657-70-3.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: (4-propylphenyl)Methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (4-propylphenyl)Methanol(82657-70-3)
• EPA Substance Registry System: (4-propylphenyl)Methanol(82657-70-3)

Safety Data

• Hazardous Substances Data: 82657-70-3(Hazardous Substances Data)

Usage

Description

(4-propylphenyl)Methanol, also known as 4-(propylphenyl)methanol or 4-isopropylbenzyl alcohol, is an aromatic alcohol with the chemical formula C10H14O and a molecular weight of 150.22 g/mol. It is a versatile and valuable chemical compound commonly used in the synthesis of pharmaceuticals, organic compounds, fragrance ingredients in personal care products and perfumes, and in the production of polymers and resins.

Uses

Used in Pharmaceutical Industry:
(4-propylphenyl)Methanol is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs and improve the efficacy of existing ones.
Used in Fragrance Industry:
(4-propylphenyl)Methanol is used as a fragrance ingredient in personal care products and perfumes for its aromatic properties, enhancing the scent profiles of these products.
Used in Polymer and Resin Production:
(4-propylphenyl)Methanol is used in the production of polymers and resins for its ability to improve the properties of these materials, such as durability and stability.
Used in Organic Compound Synthesis:
(4-propylphenyl)Methanol is used as a building block in the synthesis of various organic compounds for its versatility in forming different chemical structures and enhancing their properties.

Upstream product

• 28785-06-0 4-n-propylbenzaldehyde 
• 2438-05-3 4-n-propylbenzoic acid 
• 52710-27-7 4-propylbenzoyl chloride 
• 1093190-16-9 [2-(4-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)ethynyl]trimethylsilane 
• 275386-60-2 4-(hydroxymethyl)-1-(trimethylsilylethynyl)benzene 
• 1093190-17-0 tert-butyl[(4-ethynylphenyl)methoxy]dimethylsilane 
• 1360803-31-1 tert-butyldimethyl((4-(prop-1-yn-1-yl)benzyl)oxy)silane 
• 1360803-32-2 tert-butyldimethyl((4-propylbenzyl)oxy)silane 
• 619-42-1 4-methoxycarbonylphenyl bromide 
• 75867-41-3 4-trimethylsilanylethynyl-benzoic acid methyl ester 
• 1004992-92-0 1-(4-(hydroxymethyl)phenyl)propan-1-ol 
• 87736-74-1 4-(tert-butyldimethylsiloxymethyl)bromobenzene 

Downstream Products

• 126156-22-7 (2-Iodo-4-propyl-phenyl)-methanol 
• 91062-39-4 1-(Bromomethyl)-4-propylbenzene 
• 950508-67-5 2-(4-n-propylphenyl)-3-phenylpropan-2-one 
• 3166-98-1 (4-n-propylphenyl)acetonitrile 
• 126156-25-0 2-iodo-4-n-propyl-benzoic acid 
• 126156-30-7 2-iodoso-4-n-propylbenzoic acid 
• 3166-97-0 1-(Chloromethyl)-4-propylbenzene 
• 1224714-75-3 N-(1-{6-[(4-propylbenzyl)oxy]-1-benzofuran-3-yl}ethyl)acetamide 
• 1224716-84-0 4-propylbenzyl methanesulfonate 
• 1360803-33-3 1-(iodomethyl)-4-propylbenzene 
• 1360803-34-4 methyl 2-((4-propylbenzyl)amino)acetate 
• 26114-12-5 2-(4-propylphenyl)acetic acid 
• 1360803-35-5 methyl 2-(N-(4-propylbenzyl)-2-(4-propylphenyl)acetamido)acetate 
• 1360803-36-6 2-(N-(4-propylbenzyl)-2-(4-propylphenyl)acetamido)acetic acid 

Relevant articles and documents

Chemoselective Deoxygenation of 2° Benzylic Alcohols through a Sequence of Formylation and B(C6F5)3-Catalyzed Reduction

A sequence of formylation and B(C6F5)3-catalyzed reduction of the resulting formate with Et3SiH enables the chemoselective deoxygenation of secondary benzylic alcohols. Primary benzylic and tertiary non-benzylic alcohols are not reduced by this protocol. The formyl group fulfills a double role as activator and self-sacrificing protecting group. The deoxygenation of these formates is fast and can be carried out in the presence of other potentially reducible groups. Neighboring-group participation was found in the deoxygenation of certain diol motifs.

BENZOXAZOLONE DERIVATIVES AS ACID CERAMIDASE INHIBITORS, AND THEIR USE AS MEDICAMENTS

The present invention relates to benzoxazolone derivatives as acid ceramidase inhibitors, pharmaceutical compositions containing these inhibitors and methods of inhibiting acid ceramidase for the treatment of disorders in which modulation of the levels of ceramide is clinically relevant. The invention also provides benzoxazolone derivatives for use as a medicament in the treatment of cancer, inflammation, pain, inflammatory pain or pulmonary diseases.

CARBAMATE DERIVATIVES OF LACTAM BASED N-ACYLETHANOLAMINE ACID AMIDASE (NAAA) INHIBITORS

Described herein are compounds and pharmaceutical compositions which inhibit N-acylethanolamine acid amidase (NAAA). Described herein are methods for synthesizing the compounds set forth herein and methods for formulating these compounds as pharmaceutical compositions which include these compounds. Also described herein are methods of inhibiting NAAA in order to sustain the levels of palmitoylethanolamide (PEA) and other N-acylethanolamines (NAE) that are substrates for NAAA, in conditions characterized by reduced concentrations of NAE. Also, described here are methods of treating and ameliorating pain, inflammation, inflammatory diseases, and other disorders in which modulation of fatty acid ethanolamides is clinically or therapeutically relevant or in which decreased levels of NAE are associated with the disorder.