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57332-84-0

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57332-84-0 Usage

Description

Ethyl 3-bromo-2-oxobutyrate, also known as Ethyl α-bromoethylglyoxalate, is a chemical compound with the molecular formula C7H9BrO3. It is a clear, colorless oil at room temperature and is used in the synthesis of various chemical compounds, particularly in the field of pharmaceuticals and medical imaging.

Uses

Used in Pharmaceutical Industry:
Ethyl 3-bromo-2-oxobutyrate is used as a key intermediate in the synthesis of potential positron emission tomography (PET) tracers for neuropeptide Y Y1 receptors. These tracers are essential for studying the role of neuropeptide Y Y1 receptors in various physiological and pathological processes, including obesity, anxiety, and depression.
Used in Medical Imaging:
In the field of medical imaging, Ethyl 3-bromo-2-oxobutyrate is used as a precursor for the development of PET tracers. PET is a non-invasive imaging technique that allows for the visualization of molecular processes within the body. The tracers synthesized using Ethyl 3-bromo-2-oxobutyrate can help researchers and clinicians better understand the function and distribution of neuropeptide Y Y1 receptors, which can be crucial for the diagnosis and treatment of related conditions.
Chemical Properties:
Ethyl 3-bromo-2-oxobutyrate is a clear, colorless oil with the chemical formula C7H9BrO3. It is a stable compound at room temperature and can be easily manipulated in various chemical reactions due to its functional groups. Its chemical properties make it a versatile building block for the synthesis of more complex molecules, particularly in the pharmaceutical and medical imaging industries.

Synthesis Reference(s)

The Journal of Organic Chemistry, 67, p. 1102, 2002 DOI: 10.1021/jo010630z

Check Digit Verification of cas no

The CAS Registry Mumber 57332-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,3 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57332-84:
(7*5)+(6*7)+(5*3)+(4*3)+(3*2)+(2*8)+(1*4)=130
130 % 10 = 0
So 57332-84-0 is a valid CAS Registry Number.

57332-84-0SDS

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-2-oxobutanoate

1.2 Other means of identification

Product number -
Other names ethyl 3-bromo-2-oxobutyrate

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:57332-84-0 SDS

57332-84-0Relevant articles and documents

Novel Pyrazole-Containing Compounds Active against Mycobacterium tuberculosis

Poce, Giovanna,Consalvi, Sara,Venditti, Giulia,Alfonso, Salvatore,Desideri, Nicoletta,Fernandez-Menendez, Raquel,Bates, Robert H.,Ballell, Lluis,Barros Aguirre, David,Rullas, Joaquin,De Logu, Alessandro,Gardner, Michelle,Ioerger, Thomas R.,Rubin, Eric J.,Biava, Mariangela

, p. 1423 - 1429 (2019)

In this study, a series of 49 five-membered heterocyclic compounds containing either a pyridine- or a pyrrole-type nitrogen were synthesized and tested against Mycobacterium tuberculosis. Among them, only the 1,3,5-trisubstituted pyrazoles 5-49 exhibited

AMINOAZOLE DERIVATIVE

-

Paragraph 0186-0188, (2019/02/09)

A compound, represented by the following formula or a medically acceptable salt thereof, having an effect of regulating the activity of an androgen receptor. In the formula, X represents S, O; Z represents (Ra)n-A- (CR13R14)0-1—(CR11R12)0-1; A represents aryl, heteroaryl; R1 represents alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, aryl, arylalkyl, heterocycle, heterocyclic alkyl; R2 represents hydrogen, halogen, alkyl, cycloalkyl, phenyl; R3 represents hydrogen, halogen, alkyl, cycloalkyl, alkoxyalkyl, alkenyl, alkynyl, cycloalkenyl, aryl, arylalkyl, heterocycle, heterocyclic alkyl, acyl, cycloalkylcarbonyl, benzoyl, spiroalkyl, adamantyl, silyl, R31R32NCO—; R4 and R5 represent hydrogen, halogen, alkyl, phenyl, and cycloalkyl.

Melanin-Concentrating Hormone Receptor 1 Antagonists Lacking an Aliphatic Amine: Synthesis and Structure-Activity Relationships of Novel 1-(Imidazo[1,2-a]pyridin-6-yl)pyridin-2(1H)-one Derivatives

Igawa, Hideyuki,Takahashi, Masashi,Kakegawa, Keiko,Kina, Asato,Ikoma, Minoru,Aida, Jumpei,Yasuma, Tsuneo,Kawata, Yayoi,Ashina, Shuntaro,Yamamoto, Syunsuke,Kundu, Mrinalkanti,Khamrai, Uttam,Hirabayashi, Hideki,Nakayama, Masaharu,Nagisa, Yasutaka,Kasai, Shizuo,Maekawa, Tsuyoshi

supporting information, p. 1116 - 1139 (2016/02/23)

Aiming to discover melanin-concentrating hormone receptor 1 (MCHR1) antagonists with improved safety profiles, we hypothesized that the aliphatic amine employed in most antagonists reported to date could be removed if the bicyclic motif of the compound scaffold interacted with Asp123 and/or Tyr272 of MCHR1. We excluded aliphatic amines from our compound designs, with a cutoff value of pKa 8, and explored aliphatic amine-free MCHR1 antagonists in a CNS-oriented chemical space limited by four descriptors (TPSA, ClogP, MW, and HBD count). Screening of novel bicyclic motifs with high intrinsic binding affinity for MCHR1 identified the imidazo[1,2-a]pyridine ring (represented in compounds 6a and 6b), and subsequent cyclization of the central aliphatic amide linkage led to the discovery of a potent, orally bioavailable MCHR1 antagonist 4-[(4-chlorobenzyl)oxy]-1-(2-cyclopropyl-3-methylimidazo[1,2-a]pyridin-6-yl)pyridin-2(1H)-one 10a. It exhibited low potential for hERG inhibition and phospholipidosis induction as well as sufficient brain concentration to exert antiobesity effects in diet-induced obese rats.

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