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4282-44-4

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4282-44-4 Usage

Description

1-Iodoundecane, with the chemical formula C11H23I and the CAS number 4282-44-4, is a clear colorless liquid that is one of the volatile constituents found in the urine of a normal male mouse. It has been investigated for its reactions with fluoride sources and is known for its use in organic synthesis.

Uses

1. Used in Organic Synthesis:
1-Iodoundecane is used as a synthetic building block in the chemical industry for the creation of various organic compounds. Its unique structure and reactivity make it a valuable component in the synthesis of complex molecules.
2. Used in Research and Development:
In the field of scientific research, 1-Iodoundecane is utilized as a research compound to study its reactions with fluoride sources and to explore its potential applications in various chemical processes.
3. Used in Pharmaceutical Industry:
1-Iodoundecane may also be used in the pharmaceutical industry for the development of new drugs, as its properties can be exploited to create novel therapeutic agents.
4. Used in Analytical Chemistry:
As a volatile compound, 1-Iodoundecane can be employed in analytical chemistry for the identification and quantification of specific substances in complex mixtures, such as in the analysis of urine samples.
5. Used in Environmental Monitoring:
Due to its presence in the urine of normal male mice, 1-Iodoundecane can be used as a marker or indicator in environmental monitoring studies to assess the health of animal populations and the potential impact of environmental factors on their well-being.

Synthesis Reference(s)

Tetrahedron Letters, 9, p. 5787, 1968 DOI: 10.1016/S0040-4039(00)76351-9

Check Digit Verification of cas no

The CAS Registry Mumber 4282-44-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,8 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4282-44:
(6*4)+(5*2)+(4*8)+(3*2)+(2*4)+(1*4)=84
84 % 10 = 4
So 4282-44-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H23I/c1-2-3-4-5-6-7-8-9-10-11-12/h2-11H2,1H3

4282-44-4 Well-known Company Product Price

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  • Aldrich

  • (280046)  1-Iodoundecane  98%

  • 4282-44-4

  • 280046-50G

  • 1,726.92CNY

  • Detail

4282-44-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Iodoundecane

1.2 Other means of identification

Product number -
Other names 1-IODOUNDECANE

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:4282-44-4 SDS

4282-44-4Relevant articles and documents

Omote et al.

, p. 569 (1969)

Homogeneous catalysis, heterogeneous recycling: A new family of branched molecules with hydrocarbon or fluorocarbon chains for the Friedl?nder synthesis of quinoline under solvent-free conditions

Fang, Lei,Yu, Jianjun,Liu, Ying,Wang, Anyin,Wang, Limin

, p. 11004 - 11009 (2014/01/06)

A new family of branched catalysts with hydrocarbon or fluorocarbon chains was used to catalyze Friedl?nder reaction between 2-aminoarylketones and α-methylene ketones under solvent-free conditions in good to excellent yields. The catalysts exhibit temperature-dependent solubility and such a thermomorphic character allows them to be recovered by filtration conveniently at room temperature and reused at least five times. To some extent, the branched catalysts with hydrocarbon chains are superior to those with fluorocarbon chains, as they are cheaper and more biodegradable.

Intramolecular homolytic displacements. 30. Functional decarbonylative transformations of aldehydes via homolytically induced decomposition of unsaturated peroxyacetals

Degueil-Castaing, Marie,Moutet, Laurent,Maillard, Bernard

, p. 3961 - 3965 (2007/10/03)

Homolytically induced decompositions of unsaturated peroxyacetals, synthesized from aldehydes, gave alkoxyalkoxyl radicals that yielded alkyl radicals by rapid β-scission. The latter radicals could react with several types of "transfer agents" to smoothly bring about homolytic decarbonylative functional group transformations of aldehydes into halides, hydrocarbons, xanthates, alkanenitriles, 2-alkyl-3-chloromaleic anhydrides, 1-phenylalk-1-ynes, and ethyl 2-alkylpropenoates.

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