13686-49-2 Usage
Description
1-(2-Bromoethyl)naphthalene is a chemical compound derived from the reaction between 1-(2-hydroxyethyl)naphthalene and phosphorus tribromide. It is a clear, colorless to yellow liquid with various applications in the research field.
Uses
1. Used in Research Field:
1-(2-Bromoethyl)naphthalene is used as a reagent for various applications in the research field, including Western blotting, immunoprecipitation, and as an immunogen and purification agent.
2. Used in Western Blotting:
In the application industry of molecular biology and biochemistry, 1-(2-Bromoethyl)naphthalene is used as a component in Western blotting for the detection and analysis of specific proteins in a sample.
3. Used in Immunoprecipitation:
In the field of immunology, 1-(2-Bromoethyl)naphthalene is used as a reagent in immunoprecipitation, a technique used to isolate and analyze specific proteins that interact with a particular antibody.
4. Used as an Immunogen:
In the field of vaccine development and immunology, 1-(2-Bromoethyl)naphthalene is used as an immunogen to stimulate an immune response, which can be useful for the development of diagnostic tools and vaccines.
5. Used in Purification Processes:
In the field of chemical and biochemical purification, 1-(2-Bromoethyl)naphthalene is used as a reagent in various purification processes to separate and isolate specific compounds or proteins.
Check Digit Verification of cas no
The CAS Registry Mumber 13686-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,8 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13686-49:
(7*1)+(6*3)+(5*6)+(4*8)+(3*6)+(2*4)+(1*9)=122
122 % 10 = 2
So 13686-49-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H11Br/c13-9-8-11-6-3-5-10-4-1-2-7-12(10)11/h1-7H,8-9H2
13686-49-2Relevant articles and documents
Promotion of Appel-type reactions by N-heterocyclic carbenes
Hussein, Mohanad A.,Nguyen, Thanh Vinh
supporting information, p. 7962 - 7965 (2019/07/12)
N-Heterocyclic carbenes (NHCs) have been extensively used as a versatile class of catalysts and ligands in organocatalytic and organometallic chemistry. However, there are only a small number of synthetic applications where they act as reagents. Here we demonstrate that NHCs can be used as stoichiometric redox reagents for Appel-type halogenation reactions of alcohols. This new reactivity reveals a fresh and interesting aspect and enriches the chemistry of NHCs in an underexplored area. The potential of performing this chemical transformation at the catalytic level using an NHC-oxide derivative is also investigated.
FUNCTIONALISED AND SUBSTITUTED INDOLES AS ANTI-CANCER AGENTS
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Page/Page column 58; 59, (2016/02/05)
The present invention relates to anti-tropomyosin compounds, processes for their preparation, and methods for treating or preventing a disease or disorder, such as a proliferative disease (preferably cancer), using compounds of the invention.
Indium(III)-catalyzed one-pot synthesis of alkyl cyanides from carboxylic Acids
Moriya, Toshimitsu,Shoji, Kohei,Yoneda, Shinichiro,Ikeda, Reiko,Konakahara, Takeo,Sakai, Norio
, p. 3233 - 3238 (2013/12/04)
The one-pot preparation of alkyl cyanides from carboxylic acids via alkyl iodides or alkyl bromides, which were in situ generated either by indium(III)-catalyzed reductive iodination or bromination of carboxylic acids, is described. Georg Thieme Verlag Stuttgart New York.
