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(2-IODOETHYL) CYCLOPROPANE, with the molecular formula C5H9I, is a chemical compound that features a cyclopropane ring, a cyclic hydrocarbon, connected to an iodine atom through an ethyl group. (2-IODOETHYL) CYCLOPROPANE is primarily utilized in the realm of organic synthesis, serving as a synthetic reagent in chemical research and development.

335449-19-9

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335449-19-9 Usage

Uses

Used in Organic Synthesis:
(2-IODOETHYL) CYCLOPROPANE is used as a synthetic reagent for its role in chemical research and development. It is particularly valuable in the creation of new organic compounds, where its unique structure and reactivity contribute to the synthesis process.
Used in Chemical Research and Development:
In the field of chemical research and development, (2-IODOETHYL) CYCLOPROPANE is used as a key component in the synthesis of various chemical entities. Its application is crucial for advancing the understanding of chemical reactions and the creation of novel compounds with potential applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 335449-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,4,4 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 335449-19:
(8*3)+(7*3)+(6*5)+(5*4)+(4*4)+(3*9)+(2*1)+(1*9)=149
149 % 10 = 9
So 335449-19-9 is a valid CAS Registry Number.

335449-19-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-iodoethylcyclopropane

1.2 Other means of identification

Product number -
Other names 2-cyclopropylethyl iodide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:335449-19-9 SDS

335449-19-9Upstream product

335449-19-9Relevant academic research and scientific papers

NITROGEN-CONTAINING CONDENSED HETEROCYCLIC COMPOUND

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Paragraph 0383, (2014/02/15)

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.

ARYLSULFONYLHYDROXAMIC ACID AND AMIDE DERIVATIVES AND THEIR USE AS PROTEASE INHIBITORS

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Page 170-171, (2010/02/05)

This invention is directed generally to hydroxamic acid and amide compounds (including salts of such compounds), and, more particularly, to aryl- and heteroaryl--arylsulfonylmethyl hydroxamic acids and amides that, inter alia, inhibit protease activity, particularly matrix metalloproteinase (also known as "matrix metalloprotease" or "MMP") activity and/or aggrecanase activity. These compounds generally correspond in structure to formula (I): wherein Al, A2, A3, El, E2, E3, and E4 are as defined in this patent. This invention also is directed to compositions of such compounds, intermediates for the syntheses of such compounds, methods for making such compounds, and methods for treating conditions associated with MMP activity and/or aggrecanase activity, particularly pathological conditions.

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