92948-25-9

Usage

Molecular Structure

1-Pentanol molecule with a chlorine atom attached to the fifth carbon and a 4-methylbenzenesulfonate group.

Usage

Commonly used as an intermediate in the synthesis of various organic compounds, such as pharmaceuticals, agrochemicals, and dyes.

Industrial Applications

Has the potential to act as a surfactant, emulsifier, or dispersant in various industrial applications.

Solvent

Can be used as a solvent in organic reactions.

Component

Used as a component in the formulation of various consumer products.

Importance

Is important in the field of organic chemistry and has a range of potential industrial and commercial applications.

Upstream product

• 142-68-7 TETRAHYDROPYRANE 
• 98-59-9 p-toluenesulfonyl chloride 
• 5259-98-3 5-chloropentan-1-ol 

Downstream Products

• 54512-75-3 1-bromo-5-chloropentane 
• 1160105-89-4 C₁₀H₂₂ 
• 1224161-11-8 (R)-7-methylnonyl chloride 
• 1253597-04-4 8-cyclohexyloctyl 4-methylbenzenesulfonate 

Relevant academic research and scientific papers

New efficient imidazolium aldoxime reactivators for nerve agent-inhibited acetylcholinesterase

Herein, we described a new class of uncharged non-pyridinium reactivators for nerve agent-inhibited acetylcholinesterase (AChE). Based on a dual site binding strategy, we conjugated the imidazolium aldoxime to different peripheral site ligands (PSLs) of A

Pheromone synthesis. Part 243: Synthesis and biological evaluation of (3R,13R,1′S)-1′-ethyl-2′-methylpropyl 3,13-dimethylpentadecanoate, the major component of the sex pheromone of Paulownia bagworm, Clania variegata, and its stereoisomers

All of the four stereoisomers of (1′S)-1′-ethyl-2′-methylpropyl 3,13-dimethylpentadecanoate, the major component of the female sex pheromone of Clania variegata, were synthesized by employing olefin cross metathesis as the key reaction and starting from (R)- or (S)-2-methyl-1-butanol, (R)- or (S)-citronellal, and (S)-2-methyl-3-pentanol. Their bioassay revealed the (3R,13R,1′S)-isomer as the bioactive one, whose more efficient synthesis was achieved in two different ways by employing Wittig reaction as the key step.

3- and 4-biphenyloxyaminoalkanes and related compounds as anti-inflammatory and analgetic agents

Compounds useful for treating inflammation, swelling and associated pain, represented by the formula: STR1 and the pharmaceutically acceptable acid addition salts thereof, wherein: a is an integer of 0-3; b is an integer of 0-2; n is an integer of 3-12; each X and each Y are independently -halo, --R1, -alkoxy, or -phenyl; and B is selected from the group consisting of: --NR1 R2, --NR1 (CH2 CH2 OH), STR2 in which R1 and R2 are independently H, alkyl or cycloalkyl; R3 is H, alkyl or --CH2 CH2 OH; and m is an integer of 3-8. Novel compounds are those wherein n is at least 6 if both a and b are 0.

Anti-inflammatory guanidines

A compound having the formula STR1 where Ar=naphthyl, biphenyl, or quinolinyl; X=oxygen or NH; Y=2 to 8; R1 =phenyl, substituted phenyl, hydrogen, lower alkyl; and R2 is the same or different from R3 and is alkyl, cycloalkyl, phenyl, substituted phenyl, thiazolyl; and the pharmaceutically acceptable salts thereof. Compounds of this general formula are useful as anti-inflammatories, and as anti-psoriatic agents.