1-Pentanol, 3-mercapto-

Base Information

• Chemical Name: 1-Pentanol, 3-mercapto-
• CAS No.: 548740-99-4
• Molecular Formula: C5H12OS
• Molecular Weight: 120.216
• Mol file: 548740-99-4.mol

Synonyms:3-mercaptopentanol;3-Ethyl mercapto propanol;1-Pentanol,3-mercapto;3-mercaptopentan-1-ol;

Chemical Property of 1-Pentanol, 3-mercapto-

Chemical Property:

• PSA: 59.03000
• LogP: 1.07720

Purity/Quality:

99% ^*data from raw suppliers

3-Mercaptopentan-1-ol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Use Description: 1-Pentanol, 3-mercapto-, is a versatile chemical compound with diverse applications in various fields. In organic synthesis and materials science, it serves as a valuable building block for creating specialized molecules and polymers, contributing to the development of innovative materials used in coatings, adhesives, and sensors, enhancing material properties and functionality. In analytical chemistry, it functions as a reagent for the precise detection and quantification of specific ions or molecules, aiding in accurate chemical analysis and identification. Additionally, in the realm of chemical research, it serves as a model compound for studying the behavior of thiol derivatives, advancing our understanding of organic chemistry and reaction mechanisms. Its applications in materials science, analytical chemistry, and chemical research highlight its importance in driving material innovation, supporting precise analysis, and expanding our knowledge of chemical processes within these diverse domains.

Technology Process of 1-Pentanol, 3-mercapto-

There total 4 articles about 1-Pentanol, 3-mercapto- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

thioacetic acid S-(1-ethyl-3-oxopropyl) ester (932365-59-8) → 3-mercaptopentan-1-ol (548740-99-4)

Guidance literature:

With lithium aluminium tetrahydride; In diethyl ether; at 20 ℃; Inert atmosphere; Cooling with ice;

DOI:10.1021/jf062582v

Reference yield:

N-[3-mercaptopentanoyl]-4-isopropyloxazolidin-2-one → 3-mercaptopentan-1-ol (548740-99-4)

Guidance literature:

With sodium tetrahydroborate; In tetrahydrofuran; water; at 20 ℃;

DOI:10.1021/ja0654027

Reference yield:

3-(3-mercapto-pentanoyl)-oxazolidin-2-one → dimethylenecyclourethane (497-25-6) + 3-mercaptopentan-1-ol (548740-99-4)

Guidance literature:

With sodium tetrahydroborate; In tetrahydrofuran; water; at 20 - 25 ℃;

DOI:10.1021/ja015860+

upstream raw materials:

thioacetic acid S-(1-ethyl-3-oxopropyl) ester

Refernces

• 1、 Palomo, Claudio,Oiarbide, Mikel,Lopez, Rosa,Gonzalez, Pedro B.,Gomez-Bengoa, Enrique,Saa, Jose M.,Linden, Anthony. "Intramolecular sulfur transfer in N-enoyl oxazolidine-2-thiones promoted by Bronsted acids. Practical asymmetric synthesis of β-mercapto carboxylic acids and mechanistic insights". . p. 15236 - 15247. Retrieved 2007/10/03.