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6937-16-2

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6937-16-2 Usage

Description

Ethyl 4-aminobutyrate hydrochloride is a chemical compound derived from the neurotransmitter gamma-aminobutyric acid (GABA), commonly utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has been studied for its potential therapeutic applications in neurological disorders and as an anesthetic, while also serving as a valuable research tool in biochemical studies and a precursor in the synthesis of novel compounds. Due to its potential hazards upon ingestion, inhalation, or skin contact, careful handling is advised.

Uses

Used in Pharmaceutical Industry:
Ethyl 4-aminobutyrate hydrochloride is used as an intermediate in the production of pharmaceuticals for its potential applications in treating neurological disorders. Its GABAergic properties make it a promising candidate for the development of medications targeting such conditions.
Used in Agrochemical Industry:
In the agrochemical sector, Ethyl 4-aminobutyrate hydrochloride is employed as an intermediate in the synthesis of agrochemicals, potentially contributing to the development of new pesticides or other agricultural products.
Used in Research and Development:
Ethyl 4-aminobutyrate hydrochloride is used as a research tool in biochemical studies, aiding scientists in understanding the mechanisms of neurotransmission and exploring its potential as a precursor in the synthesis of novel compounds for various applications.
Used in Anesthetic Applications:
Ethyl 4-aminobutyrate hydrochloride is studied for its potential use as an anesthetic, leveraging its effects on the central nervous system to provide pain relief during medical procedures.

Check Digit Verification of cas no

The CAS Registry Mumber 6937-16-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6937-16:
(6*6)+(5*9)+(4*3)+(3*7)+(2*1)+(1*6)=122
122 % 10 = 2
So 6937-16-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO2/c1-2-9-6(8)4-3-5-7/h2-5,7H2,1H3

6937-16-2 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (E0924)  Ethyl 4-Aminobutyrate Hydrochloride  >98.0%(N)(T)

  • 6937-16-2

  • 5g

  • 140.00CNY

  • Detail
  • TCI America

  • (E0924)  Ethyl 4-Aminobutyrate Hydrochloride  >98.0%(N)(T)

  • 6937-16-2

  • 25g

  • 450.00CNY

  • Detail
  • Alfa Aesar

  • (L06863)  Ethyl 4-aminobutyrate hydrochloride, 98%   

  • 6937-16-2

  • 5g

  • 177.0CNY

  • Detail
  • Alfa Aesar

  • (L06863)  Ethyl 4-aminobutyrate hydrochloride, 98%   

  • 6937-16-2

  • 25g

  • 427.0CNY

  • Detail

6937-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4-Aminobutyrate Hydrochloride

1.2 Other means of identification

Product number -
Other names ethyl 4-aminobutanoate,hydrochloride

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:6937-16-2 SDS

6937-16-2Relevant articles and documents

Modified Conjugated Diene-Based Polymer And Method Of Preparing The Same

-

Paragraph 0195-0197, (2020/05/06)

The present invention relates to a modifier represented by Formula 1, a method of preparing the same, a modified conjugated diene-based polymer having a high modification ratio which includes a modifier-derived functional group, and a method of preparing the polymer.

Chiral 1,5-disubstituted 1,3,5-hexahydrotriazine-2-N-nitroimine analogues as novel potent neonicotinoids: Synthesis, insecticidal evaluation and molecular docking studies

Sun, Chuanwen,Zhu, Jun,Wang, Haifeng,Jin, Jia,Xing, Jiahua,Yang, Dingrong

experimental part, p. 11 - 20 (2011/02/27)

A new series of 1,5-disubstituted 1,3,5-hexahydrotriazine-2-N-nitroimines (4a-4x) were designed and synthesized as novel chiral neonicotinoid analogues. The single-crystal structure of 4n was further determined by X-ray diffraction, and its S configuration was confirmed. Preliminary bioassay showed that compound 4e, 4k, 4u, 4v exhibited excellent insecticidal activities at 100 mg/L, while 4k had >90% mortality at 10 mg/L, which suggested it could be used as a lead for future development. Modeling the inhibitor-nAChR complexes by molecular docking studies explained the structure-activity relationships observed in vitro, and revealed an intriguing molecular binding mode at the active site of nAChR, which raised the possibility that these analogues may arbitrate their insecticidal activity through a mechanism other than imidacloprid.

Anthranilic acid based CCK1 receptor antagonists: Blocking the receptor with the same 'words' of the endogenous ligand

Lassiani, Lucia,Pavan, Michela V.,Berti, Federico,Kokotos, George,Markidis, Theodoros,Mennuni, Laura,Makovec, Francesco,Varnavas, Antonio

experimental part, p. 2336 - 2350 (2009/09/05)

The anthranilic acid diamides represent the more recent class of nonpeptide CCK1 receptor antagonists. This class is characterized by the presence of anthranilic acid, used as a molecular scaffold, and two pharmacophores selected from the C-terminal tetrapeptide of CCK. The lead compound coded VL-0395, endowed with sub-micromolar affinity towards CCK1 receptors, was characterized by the presence of Phe and 2-indole moiety at the C- and N-termini of anthranilic acid, respectively. Herein we describe the first step of the anthranilic acid C-terminal optimization using, instead of Phe, aminoacids belonging to the primary structure of CCK-8 and other not coded residues. Thus we demonstrate that the CCK1 receptor affinity depends on the nature of the aminoacidic side chain as well as that the free carboxy group of the alpha-aminoacids is crucial for the binding. The R enantiomers of the most active compounds represent the eutomers of this class of antagonists confirming thus the stereo preference of the receptor. Moreover this SAR study demonstrates that the receptor binding pocket, that host the aminoacidic side chain, results much more tolerant respect to that accommodating the indole ring. As a result, an appropriate variation of the aminoacidic side chain could provide a better CCK1 receptor affinity diorthosis.

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