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1860-44-2

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1860-44-2 Usage

General Description

11-Chloro-undecanoic acid is a chemical compound with the molecular formula C11H21ClO2. It is a chlorinated derivative of undecanoic acid, which is a fatty acid commonly found in natural fats and oils. 11-Chloro-undecanoic acid is a white crystalline solid at room temperature and is insoluble in water. It is primarily used in the production of surfactants, emulsifiers, and lubricants, and also serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals. This chemical compound is classified as a chloroalkanoic acid, and its properties and applications make it an important ingredient in various industrial processes.

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)

1860-44-2SDS

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 11-chloroundecanoic acid

1.2 Other means of identification

Product number -
Other names 11-CHLORO-UNDECANOIC ACID

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:1860-44-2 SDS

1860-44-2Relevant articles and documents

-

Saotome,K. et al.

, p. 480 - 484 (1966)

-

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.

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