80433-91-6

Basic information

• Product Name: (1S,2S)-1,2,3,4-tetrahydrochrysene-1,2-diyl diacetate
• CAS NO: 80433-91-6
• Molecular Formula: C₂₂H₂₀O₄
• Molecular Weight: 348.3918
• Mol File: 80433-91-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 514.4°C at 760 mmHg
• Flash Point: 262°C
• Density: 1.26g/cm³
• Vapor Pressure: 1.08E-10mmHg at 25°C
• Refractive Index: 1.647
• CAS DataBase Reference: (1S,2S)-1,2,3,4-tetrahydrochrysene-1,2-diyl diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S)-1,2,3,4-tetrahydrochrysene-1,2-diyl diacetate(80433-91-6)
• EPA Substance Registry System: (1S,2S)-1,2,3,4-tetrahydrochrysene-1,2-diyl diacetate(80433-91-6)

Safety Data

• Hazardous Substances Data: 80433-91-6(Hazardous Substances Data)

Usage

Description

(1S,2S)-1,2,3,4-tetrahydrochrysene-1,2-diyl diacetate is a diester derivative of (1S,2S)-1,2,3,4-tetrahydrochrysene, a member of the chrysene family, which is a group of polycyclic aromatic hydrocarbons (PAHs). It is composed of two acetic acid molecules attached to the (1S,2S)-1,2,3,4-tetrahydrochrysene core. (1S,2S)-1,2,3,4-tetrahydrochrysene-1,2-diyl diacetate is found in sources such as crude oil, coal tar, and other fossil fuel combustion products. Due to its potential toxicity and carcinogenicity, it is of interest in chemical research, environmental analysis, and may have potential applications in pharmaceuticals or other industrial products.

Uses

Used in Chemical Research:
(1S,2S)-1,2,3,4-tetrahydrochrysene-1,2-diyl diacetate is used as a research compound for studying the properties and behavior of PAHs and their derivatives. Its unique structure allows scientists to investigate its chemical reactivity and potential interactions with other molecules.
Used in Environmental Analysis:
As a component of fossil fuel combustion products, (1S,2S)-1,2,3,4-tetrahydrochrysene-1,2-diyl diacetate is used in environmental analysis to monitor and assess the presence of PAHs in air, water, and soil samples. This helps in understanding the impact of pollution and developing methods for environmental remediation.
Used in Pharmaceutical Development:
The diacetate derivative of (1S,2S)-1,2,3,4-tetrahydrochrysene may have potential applications in the development of pharmaceuticals. Its unique chemical properties could be harnessed to create new drugs or improve the delivery and efficacy of existing medications.
Used in Industrial Product Development:
(1S,2S)-1,2,3,4-tetrahydrochrysene-1,2-diyl diacetate may also have potential uses in the development of new industrial products. Its properties could be utilized in the creation of novel materials or processes, contributing to advancements in various industries.

Upstream product

• 80446-24-8 ((1R,2S,5R)-2-Isopropyl-5-methyl-cyclohexyloxy)-acetic acid (1S,2S)-2-[2-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyloxy)-acetoxy]-1,2,3,4-tetrahydro-chrysen-1-yl ester 
• 67175-75-1 (+/-)-trans-1,2-dihydroxy-1,2,3,4-tetrahydrochrysene 
• 108-24-7 acetic anhydride 
• 80433-89-2 (-)-trans-(1S,2S)-1,2-dihydroxy-1,2,3,4-tetrahydrochrysene 

Downstream Products

• 80433-95-0 trans-Chrysene-1,2-Dihydrodiol 
• 80433-82-5 (-)-(1S,2R,3R,4S)-1,2-dihydroxy-3,4-epoxy-1,2,3,4-tetrahydrochrysene 
• 80433-80-3 (+)-(1S,2R,3S,4R)-1,2-dihydroxy-3,4-epoxy-1,2,3,4-tetrahydrochrysene 
• 80433-97-2 (+)-trans-(1S,2S)-1,2-diacetoxy-1,2-dihydrochrysene 

Relevant articles and documents

Synthesis of the Enantiomeric Bay-Region Diol Epoxides of Benzanthracene and Chrysene

Both trans-3,4-dihydroxy-3,4-dihydrobenzanthracene and trans-1,2-dihydroxy-1,2-dihydrochrysene are known proximate carcinogens of their respective hydrocarbons.The present study describes the synthesis of their (+)- and (-)-enantiomers as well as the d