38727-09-2

Basic information

• Product Name: (+-)-2(a)-Amino-3(a)-phenyl-trans-decalin methanesulfonate
• Synonyms: (+-)-2(a)-Amino-3(a)-phenyl-trans-decalin methanesulfonate
• CAS NO: 38727-09-2
• Molecular Formula: C17H27NO3S
• Molecular Weight: 325.46618
• Mol File: 38727-09-2.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 349.7°Cat760mmHg
• Flash Point: 169.8°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 4.62E-05mmHg at 25°C
• CAS DataBase Reference: (+-)-2(a)-Amino-3(a)-phenyl-trans-decalin methanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: (+-)-2(a)-Amino-3(a)-phenyl-trans-decalin methanesulfonate(38727-09-2)
• EPA Substance Registry System: (+-)-2(a)-Amino-3(a)-phenyl-trans-decalin methanesulfonate(38727-09-2)

Safety Data

• Hazardous Substances Data: 38727-09-2(Hazardous Substances Data)

Usage

Description

(+-)-2(a)-Amino-3(a)-phenyl-trans-decalin methanesulfonate is a chemical compound that features a decalin ring system with a trans-configuration and a phenyl group attached to one of the carbon atoms. It also includes an amino group and a methanesulfonate group, which contribute to its solubility in organic solvents and its utility in various applications.

Uses

Used in Organic Synthesis:
(+-)-2(a)-Amino-3(a)-phenyl-trans-decalin methanesulfonate is used as a chiral building block in organic synthesis for the preparation of pharmaceuticals and other biologically active molecules. Its asymmetric carbon in the decalin ring provides the compound with chirality, making it a valuable component in the synthesis of chiral compounds.
Used in Research:
In research settings, (+-)-2(a)-Amino-3(a)-phenyl-trans-decalin methanesulfonate serves as a versatile compound for studying the properties and reactions of chiral molecules. Its unique structure allows scientists to explore its potential applications in the development of new drugs and other advanced materials.
Used in Pharmaceutical Development:
(+-)-2(a)-Amino-3(a)-phenyl-trans-decalin methanesulfonate is utilized in the pharmaceutical industry as a key intermediate in the synthesis of various drugs. Its ability to enhance solubility and its chiral nature make it an essential component in the creation of new medications with improved efficacy and selectivity.
Used in the Synthesis of Biologically Active Molecules:
(+-)-2(a)-Amino-3(a)-phenyl-trans-decalin methanesulfonate is also employed in the synthesis of biologically active molecules, such as agrochemicals and other specialty chemicals. Its unique structure and properties enable the development of novel compounds with specific biological activities, contributing to advancements in various industries.

InChI:InChI=1/C16H23N.CH4O3S/c17-16-11-14-9-5-4-8-13(14)10-15(16)12-6-2-1-3-7-12;1-5(2,3)4/h1-3,6-7,13-16H,4-5,8-11,17H2;1H3,(H,2,3,4)/t13-,14-,15+,16+;/m1./s1