1860-44-2 Usage
Uses
Used in Surfactant Production:
11-Chloro-undecanoic acid is used as a raw material for the production of surfactants, which are compounds that lower the surface tension between two liquids or a liquid and a solid. These surfactants are essential in various applications, such as detergents, cleaning agents, and personal care products, due to their ability to stabilize emulsions and foams.
Used in Emulsifier Production:
This chemical compound is also used as a key ingredient in the production of emulsifiers. Emulsifiers are substances that help mix two immiscible liquids, such as oil and water, by reducing the interfacial tension between them. They are widely used in the food, cosmetics, and pharmaceutical industries to create stable emulsions.
Used in Lubricant Production:
11-Chloro-undecanoic acid is utilized as a component in the formulation of lubricants, which are substances that reduce friction between two surfaces in mutual contact. Lubricants are crucial in various industries, including automotive, machinery, and manufacturing, to ensure smooth operation and prevent wear and tear.
Used in Pharmaceutical Synthesis:
As an intermediate in the synthesis of pharmaceuticals, 11-chloro-undecanoic acid plays a vital role in the development of new drugs and medications. Its unique properties allow it to be incorporated into various drug formulations, contributing to their effectiveness and safety.
Used in Agrochemical Synthesis:
In the agrochemical industry, 11-chloro-undecanoic acid is used as an intermediate in the synthesis of various agrochemicals, such as pesticides and herbicides. These products are essential for maintaining crop health and increasing agricultural productivity.
Check Digit Verification of cas no
The CAS Registry Mumber 1860-44-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,6 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1860-44:
(6*1)+(5*8)+(4*6)+(3*0)+(2*4)+(1*4)=82
82 % 10 = 2
So 1860-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H21ClO2/c12-10-8-6-4-2-1-3-5-7-9-11(13)14/h1-10H2,(H,13,14)
1860-44-2Relevant academic research and scientific papers
Spicamycin derivatives and their use as anticancer agents
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, (2008/06/13)
Spicamycin derivative represented by the formula (I) or a salt thereof: STR1 wherein R represents specific diverse substituents, for example, a linear alkadienyl having from 11 to 13 carbon atoms, and R1 and R2 respectively represent H or OH. Examples of specific compounds are 6-[4'-N-(N'-trans,trans 2,4-tridecadienoylglycyl)spicaminyl-amino]purine, and 6-[4'-N-(N'-trans,trans-2,4 dodecadienyoly glycyl) spicaminyl-amino]purine. Comopunds according to this invention are useful as a pharmaceutical for inhibition of a tumor, for example, human colon cancer.
INTERPRETING SUBSTITUENT EFFECTS ON THE CRYSTAL PACKING OF LONG-CHAIN DIACYL PEROXXIDES. THE CRYSTAL STRUCTURES OF DI(11-BROMOUNDECANOYL) PEROXIDE AND DI(UNDECANOYL) PEROXIDE
McBride, J. Michael,Bertman, Steven B.,Cioffi, Donna Z.,Segmuller, Brigitte E.,Weber, Bruce A.
, p. 1 - 24 (2007/10/02)
Although crystals of di(11-bromoundecanoyl) peroxide and di(undecanoyl) peroxide have different space groups (P43212 and C2221), the molecules pack in almost identical layers.They differ only in the nature of stacking across interfaces involving the terminal groups.Because the 90 deg twist about the O-O bond locks neighboring molecules together within the layer, each peroxide shows a single solid phase from 5K to the melting point.Analysis of the stacking pattern in terms of the six possible orientational relationships suggests special stability for an L-shaped motif of C-Br...Br-C.Other substituents create different stackings of the same layer structure to give three crystal classes and five space groups among 14 compounds.Unsymmetrical peroxides are useful both for forcing a variety of substituted chains (particularly odd-even homologues) to pack with identical layer structures, and for controlling the stacking pattern.Because structural differences are localized in the vicinity of the substituents, this series of "substitutional polytypes" will allow systematic investigation of substituent effects on the physical and chemical properties of solids.
