90989-08-5

Basic information

• Product Name: 2 - thia - bicyclo[3.1.0]hex - 3 - ene - 6 - carboxylic acid ethyl ester
• Synonyms: 2 - thia - bicyclo[3.1.0]hex - 3 - ene - 6 - carboxylic acid ethyl ester;Ethyl 2-thiabicyclo[3.1.0]hex-3-ene-6-carboxylate
• CAS NO: 90989-08-5
• Molecular Formula: C8H10O2S
• Molecular Weight: 170.2288
• Mol File: 90989-08-5.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2 - thia - bicyclo[3.1.0]hex - 3 - ene - 6 - carboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2 - thia - bicyclo[3.1.0]hex - 3 - ene - 6 - carboxylic acid ethyl ester(90989-08-5)
• EPA Substance Registry System: 2 - thia - bicyclo[3.1.0]hex - 3 - ene - 6 - carboxylic acid ethyl ester(90989-08-5)

Safety Data

• Hazardous Substances Data: 90989-08-5(Hazardous Substances Data)

Usage

Ester derivative

2-thia-bicyclo[3.1.0]hex-3-ene-6-carboxylic acid
The compound is derived from the parent compound 2-thia-bicyclo[3.1.0]hex-3-ene-6-carboxylic acid by replacing the hydroxyl group (-OH) with an ethoxy group (-OCH3).

Bicyclic structure

The compound has a bicyclic ring system, which means it consists of two fused rings in its molecular structure.

Presence of sulfur atom

The compound contains a sulfur atom in its ring structure, which contributes to its unique chemical properties and reactivity.

Organic synthesis and pharmaceutical research

The compound is commonly used as a building block in organic synthesis and pharmaceutical research for the synthesis of various organic compounds and drug candidates.

Unique molecular structure and functional groups

The compound's molecular structure and functional groups make it a useful intermediate for the preparation of diverse bioactive molecules.

Versatile nature

Due to its unique structure and reactivity, the compound has potential applications in the fields of medicinal chemistry and drug discovery.

Upstream product

• 188290-36-0 thiophene 
• 623-73-4 diazoacetic acid ethyl ester 

Relevant articles and documents

PROCESS FOR THE PRODUCTION OF CYCLOPROPANE DERIVATIVES

A process for the preparation of a cyclopropane derivative of Formula (I), by reacting an olefin of Formula (II), with a carbene of the formula :CR1 R2, in a reaction vessel, optionally in the presence of a solvent, wherein, R1 and R2 are each independently hydrogen, C1-C6 alkyl, C2-C6 alkenyl, aryl, heteroaryl, heterocyclyl, carbocyclyl, heterocyclyl, -C(O)R7 or -NR82; R3, R4, R5 and R6 are each independently hydrogen, C1-C6 alkyl, C1-C6 alkoxy, C2-C6 alkenyl, aryl, aryloxy, heteroaryl, heterocyclyl, carbocyclyl, heterocyclyl, -C(O)R9, -NR102, -SR11, -S(O)R11, or -SO2R11, or R3 and R6 are as defined above and R4 and R5 together form a ring, which ring is carbocyclyl, heterocyclyl, aromatic or heteroaromatic; R7 is hydrogen, hydroxy, C1-C6 alkyl, C1-C6 alkoxy, aryl, aryloxy, heteroaryl or -NR102; R8 is hydrogen, C1-C6 alkyl, C1 -C6 alkenyl, aryl, heteroaryl, carbocyclyl or heterocyclyl; R9 is hydrogen, hydroxy, C1-C6 alkyl, C1 -C6 alkoxy, aryl, aryloxy or heteroaryl; R10 is hydrogen, C1 -C6 alkyl, C2-C6 alkenyl, aryl, heteroaryl, carbocyclyl, heterocyclyl or C(O)R12; R11 is hydrogen, C1-C6 alkyl, C2-C6 alkenyl, aryl, heteroaryl, carbocyclyl or heterocyclyl; and R12 is hydrogen, hydroxy, C1-C6 alkyl, C1-C6 alkoxy, aryl, or aryloxy, in the presence of copper metal or copper oxide, wherein the process is a continuous process.