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6271-23-4

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6271-23-4 Usage

General Description

11-Bromoundecanoic acid ethyl ester is a chemical compound that is derived from undecanoic acid. It is a colorless to pale yellow liquid that is soluble in most organic solvents. 11-BROMOUNDECANOIC ACID ETHYL ESTER is often used as a reagent in organic synthesis, particularly in the production of pharmaceuticals and other fine chemicals. It is also utilized as a potential antifungal agent due to its fungicidal activity. Additionally, 11-Bromoundecanoic acid ethyl ester can be used in the manufacture of flavors and fragrances, as well as in the production of surfactants and emulsifiers. It has a wide range of industrial applications and is an important intermediate in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 6271-23-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6271-23:
(6*6)+(5*2)+(4*7)+(3*1)+(2*2)+(1*3)=84
84 % 10 = 4
So 6271-23-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H25BrO2/c1-2-16-13(15)11-9-7-5-3-4-6-8-10-12-14/h2-12H2,1H3

6271-23-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 11-Bromoundecanoate

1.2 Other means of identification

Product number -
Other names bromoundecylinic acid ethyl ester

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:6271-23-4 SDS

6271-23-4Relevant articles and documents

KuQuinones as sensitizers for NiO based p-type dye-sensitized solar cells

Bonomo, Matteo,Sabuzi, Federica,Di Carlo, Aldo,Conte, Valeria,Dini, Danilo,Galloni, Pierluca

, p. 2769 - 2779 (2017/04/03)

A new series of KuQuinones (KuQs) have been synthesized and employed as dye-sensitizers for NiO-based p-type dye-sensitized solar cells (p-DSSCs). KuQs are pentacyclic quinoid compounds which are characterized by a fully conjugated structure that is responsible for the strong and broad absorption in the visible spectrum. The HOMO/LUMO states of KuQs considered here have matching energy levels with the upper edge of the NiO valence band and I?/I3? redox potential energy. These features render such compounds suitable for NiO sensitization in p-DSSCs. The new carboxylic acid-substituted KuQ derivatives proposed here differ in the length of the alkyl chain. The JV characteristic curves and the external quantum efficiency spectra have been recorded. The results showed that the performances of KuQ-sensitized cells were similar to that of the benchmark sensitizer erythrosine B (Ery B), despite the lack of electronic conjugation between the anchoring group and the light absorbing unit. This result led us to hypothesize that the photoinduced charge transfer between the excited KuQ dyes and the NiO electrode occurred through space and not via chemical bonds as it usually occurs in these systems. The mechanism of charge transfer through space has been supported by data from IR spectroscopy.

Preparation and properties of a novel solution of hydrogen bromide (HBr) in 1,4-dioxane: An alternative reagent to HBr gas without protic solvents

Nishio, Yuya,Mifune, Ryota,Sato, Taisuke,Ishikawa, Shin-ich,Matsubara, Hiroshi

, p. 1190 - 1193 (2017/03/02)

A solution of hydrogen bromide (HBr) in 1,4-dioxane was prepared and investigated for its ability to brominate alcohols, and hydrobrominate alkenes. This study revealed that the brominating ability of this HBr/1,4-dioxane solution is equal or superior to that of hydrobromic acid or HBr in acetic acid. The solution of HBr in 1,4-dioxane is robust, exhibiting no decomposition of the solvent, and retaining 97% of its original concentration, when kept at ?25 °C for 30 days. This solution is a liquid alternative to HBr gas without protic solvents.

Efficient Syntheses of Star-Branched, Multifunctional Mesogens

Song, Shuang,Rudick, Jonathan G.

supporting information, p. 3244 - 3247 (2015/07/15)

Star-branched molecular architectures lend themselves to convergent synthesis strategies for creating materials that combine three or more functional modalities, but these approaches require a core moiety with several reactive groups that are orthogonal t

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