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Ethyl 3-bromobenzenecarboximidoate hydrochloride is a chemical compound derived from the ester of 3-bromobenzenecarboxylic acid and ethylamine. It is characterized by its unique structure and properties, making it a valuable tool for chemists and researchers in the field of medicinal chemistry and drug discovery. The hydrochloride salt form of ethyl 3-bromobenzenecarboximidoate hydrochloride enhances its solubility in water, facilitating its handling and use in laboratory settings.

57508-63-1

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57508-63-1 Usage

Uses

Used in Organic Synthesis:
Ethyl 3-bromobenzenecarboximidoate hydrochloride is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, ethyl 3-bromobenzenecarboximidoate hydrochloride is utilized as a building block in the synthesis of new drugs. Its unique structure allows it to be incorporated into the development of potential therapeutic agents, enhancing the diversity of chemical entities available for medicinal applications.
Used in Drug Discovery:
Ethyl 3-bromobenzenecarboximidoate hydrochloride serves as a valuable tool in drug discovery, where its properties can be exploited to design and optimize compounds with desired pharmacological activities. Its versatility in chemical reactions makes it an essential component in the creation of novel drug candidates.

Check Digit Verification of cas no

The CAS Registry Mumber 57508-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,0 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57508-63:
(7*5)+(6*7)+(5*5)+(4*0)+(3*8)+(2*6)+(1*3)=141
141 % 10 = 1
So 57508-63-1 is a valid CAS Registry Number.

57508-63-1SDS

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-bromobenzenecarboximidate hydrochloride (1:1)

1.2 Other means of identification

Product number -
Other names (3-Bromophenyl)(2,2-diethoxyethyl)sulfane

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:57508-63-1 SDS

57508-63-1Relevant academic research and scientific papers

SUBSTITUTED PYRROLO[1,2-α]TRIAZINES AND RELATED COMPOUNDS AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS

-

Paragraph 00221, (2017/12/14)

The invention provides substituted pyrrolo[1,2-α]triazine compounds, related compounds, compositions containing such compounds, medical kits, and methods for using such compounds and compositions to treat medical disorders, e.g., Gaucher disease, Parkinso

METABOTROPIC GLUTAMATE RECEPTOR NEGATIVE ALLOSTERIC MODULATORS (NAMS) AND USES THEREOF

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Paragraph 00352, (2016/01/01)

Provided herein are small molecule active metabotropic glutamate subtype-2 and -3 receptor negative allosteric modulators (NAMs), compositions comprising the compounds, and methods of using the compounds and compositions.

Inhibitors of HCV replication

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Page/Page column 219-220, (2010/10/20)

Indole compounds of Formula I are described. The compounds have activity against hepatitis C virus (HCV) and are useful in treating those infected with HCV. Different forms and compositions comprising the compounds are also described as well as methods of preparing the compounds.

DNA Binding Compounds. VI. Synthesis and Characterization of 2,5'-Disubstituted Bibenzimidazoles Related to the DNA Minor Groove Hoechst 33258

Kelly, David P.,Bateman, Stuart A.,Hook, Robert J.,Martin, Roger F.,Reum, Monica E.,et al.

, p. 1751 - 1770 (2007/10/02)

A series of compounds have been synthesized in which the basic 2-phenylbibenzimidazole structure of Hoechst 33258 has been modified to include various combinations of bromo, iodo, methoxy, amino, alkylamino and nitro groups in the terminal phenyl ring.Both sequential and convergent synthetic routs have been followed using coupling reactions of both imino ethers and aldehydes to 1,2-diamines.All these compounds were characterized by a combination of f.a.b. mass spectrometry and 1H and 13C n.m.r. spectroscopy including inverse detection of long-range heteronuclear CH correlations (HMBC).

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