335449-19-9

Basic information

• Product Name: (2-IODOETHYL) CYCLOPROPANE
• Synonyms: (2-IODOETHYL) CYCLOPROPANE
• CAS NO: 335449-19-9
• Molecular Formula: C₅H₉I
• Molecular Weight: 196.02943
• Mol File: 335449-19-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 163.9±9.0 °C(Predicted)
• Appearance: /
• Density: 1.787±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: (2-IODOETHYL) CYCLOPROPANE(CAS DataBase Reference)
• NIST Chemistry Reference: (2-IODOETHYL) CYCLOPROPANE(335449-19-9)
• EPA Substance Registry System: (2-IODOETHYL) CYCLOPROPANE(335449-19-9)

Safety Data

• Hazardous Substances Data: 335449-19-9(Hazardous Substances Data)

Usage

General Description

(2-Iodoethyl) cyclopropane is a chemical compound that consists of a cyclopropane ring, which is a type of cyclic hydrocarbon, linked to an iodine atom through an ethyl group. Its molecular formula is C5H9I, indicating it contains five atoms of carbon, nine atoms of hydrogen, and one atom of iodine. The primary applications of this chemical are largely within the field of organic synthesis. Particularly, in chemical research and development, it is used as a synthetic reagent. This specialized compound can be challenging to handle as it may require controlled environments due to its reactivity with certain materials. As with many chemicals, proper safety precautions should be taken when using (2-Iodoethyl) cyclopropane due to its potential health hazards.

Upstream product

• 2566-44-1 1-cyclopropylethanol 

Downstream Products

• 639492-20-9 4-({4-[5-(2-cyclopropylethyl)pyrazin-2-yl]phenyl}sulfonyl)-N-hydroxytetrahydro-2H-pyran-4-carboxamide hydrochloride 
• 1040543-71-2 ethyl 2-(2-cyclopropylethyl)-6-(4-fluorophenyl)-5-hydroxy-3-oxo-2,3-dihydro-4-pyridazinecarboxylate 

Relevant articles and documents

NITROGEN-CONTAINING CONDENSED HETEROCYCLIC COMPOUND

There are provided compounds represented by the following general formula (I) or pharmaceutically acceptable salts of thereof, which have a superior monoacylglycerol acyltransferase 2 inhibitory action: wherein Ring A represents a partially saturated heteroaryl group, an aryl group or a heteroaryl group, RB represents a C4-18 alkyl group, a C3-8 cycloalkyl group, a partially saturated aryl group, an aryl group, or the following formula (II): wherein V represents the formula -CR11R12-, -CO-, -CO-O-, or -CO-NH-, W represents a single bond or a C1-3 alkylene group, and Ring B represents a C3-8 cycloalkyl group, a C3-8 cycloalkenyl group, a partially saturated heteroaryl group, a saturated heterocyclyl group, an aryl group, or a heteroaryl group, Y represents a nitrogen atom or the formula N+(RF), RF represents a C1-4 alkyl group, and m and n, which may be the same or different, each represent an integer of 0 or 1.