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RARECHEM AL BI 0277, with the molecular formula C13H19NO2, is a butyramide derivative also known as N-(2-Methyl-3-phenylpropyl)-butyramide. It is a chemical compound that is commonly utilized in research and development, with potential applications in pharmaceutical or industrial sectors. Due to its chemical nature, it is crucial to handle RARECHEM AL BI 0277 with care and adhere to safety protocols in laboratory environments. Further investigation and testing are necessary to fully comprehend its properties and possible uses.
Usage:
RARECHEM AL BI 0277 is used in various applications across different industries, primarily for research and development purposes. Here are some specific uses:
Used in Pharmaceutical Research and Development:
RARECHEM AL BI 0277 is used as a chemical intermediate for the synthesis of pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Industrial Research and Development:
In the industrial sector, RARECHEM AL BI 0277 is used as a research compound to explore its potential applications in various chemical processes and formulations. Its versatility and reactivity may contribute to the creation of new materials and products.
Used in Laboratory Testing and Analysis:
RARECHEM AL BI 0277 is utilized in laboratory settings for testing and analysis purposes. It can be employed to study its chemical properties, reactivity, and interactions with other compounds, which can provide valuable insights into its potential uses and applications.

23233-33-2

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23233-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23233-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,3 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23233-33:
(7*2)+(6*3)+(5*2)+(4*3)+(3*3)+(2*3)+(1*3)=72
72 % 10 = 2
So 23233-33-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H8BrFO2/c1-2-13-9(12)6-3-4-8(11)7(10)5-6/h3-5H,2H2,1H3

23233-33-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-bromo-4-fluorobenzoate

1.2 Other means of identification

Product number -
Other names Aethyl-3-brom-4-fluorobenzoat

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:23233-33-2 SDS

23233-33-2Relevant academic research and scientific papers

A facile synthesis of indolo[3,2,1-jk]carbazoles via palladium-catalyzed intramolecular cyclization

Lv, Jun,Liu, Qiancai,Tang, Jie,Perdih, Franc,Kranjc, Kristof

supporting information, p. 5248 - 5252 (2012/10/30)

A new efficient synthesis of indolo[3,2,1-jk]carbazoles by the palladium-catalyzed cyclization of N-(2-bromoaryl)carbazoles is described. The reaction involves intramolecular C-C bond formation, coupled with the cleavage of a C-X bond and a C-H bond on carbazole ring. Substitutions on N-aryl core with either electron-donating or electron-withdrawing groups are introduced, and different reaction factors for cyclization are evaluated.

COMPOUND HAVING 6-MEMBERED AROMATIC RING

-

Page/Page column 48, (2010/12/17)

An object of the present invention is to provide an agent for preventing or treating schizophrenia or the like, wherein the compound of the present invention has GPR52 agonist activity. [Means] A compound represented by the following formula (I) or salt t

Synthesis of dictyomedins using phosphazene base catalyzed diaryl ether formation

Ebisawa, Masaru,Ueno, Masahiro,Oshima, Yoshiteru,Kondo, Yoshinori

, p. 8918 - 8921 (2008/03/14)

Dictyomedins isolated from dictyostelium cellular slime molds were synthesized by using diaryl ether derivatives as key intermediates for the cyclization to dibenzofuran followed by palladium catalyzed intramolecular biaryl formation.

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