Cas no 1353964-90-5 (N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride)
N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride Chemical and Physical Properties
Names and Identifiers
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- N-((2-chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride
- AM93415
- N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride
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- Inchi: 1S/C7H9ClN2S.ClH/c8-7-10-4-6(11-7)3-9-5-1-2-5;/h4-5,9H,1-3H2;1H
- InChI Key: MVWSGCWTHWEFOB-UHFFFAOYSA-N
- SMILES: ClC1=NC=C(CNC2CC2)S1.Cl
Computed Properties
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 12
- Rotatable Bond Count: 3
- Complexity: 140
- Topological Polar Surface Area: 53.2
N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride Security Information
- Signal Word:warning
- Hazard Statement: H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
- Warning Statement: P264+P280+P305+P351+P338+P337+P313
- Safety Instruction: H303+H313+H333
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 088546-1g |
N-((2-chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride |
1353964-90-5 | 1g |
£458.00 | 2022-03-01 | ||
| Chemenu | CM497147-1g |
N-((2-Chlorothiazol-5-yl)methyl)cyclopropanaminehydrochloride |
1353964-90-5 | 97% | 1g |
$528 | 2022-09-29 |
N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride Related Literature
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Qiyuan Wu,Shangmin Xiong,Peichuan Shen,Shen Zhao,Alexander Orlov Catal. Sci. Technol., 2015,5, 2059-2064
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Alena Koukalová,?árka Pokorná,Aimee L. Boyle,Nestor Lopez Mora,Alexander Kros,Martin Hof,Radek ?achl Nanoscale, 2018,10, 19064-19073
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Xinhuan Wang,Shuangfei Cai,Cui Qi Analyst, 2017,142, 2500-2506
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Brindha J.,Balamurali M. M.,Kaushik Chanda RSC Adv., 2019,9, 34720-34734
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Gang Pan,Yi-jie Bao,Jie Xu,Tao Liu,Cheng Liu,Yan-yan Qiu,Xiao-jing Shi,Hui Yu,Ting-ting Jia,Xia Yuan,Ze-ting Yuan,Yi-jun Cao RSC Adv., 2016,6, 42109-42119
Additional information on N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride
Comprehensive Overview of N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride (CAS 1353964-90-5)
N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride (CAS 1353964-90-5) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This compound, characterized by its unique thiazole and cyclopropylamine moieties, serves as a key intermediate in the synthesis of bioactive molecules. Its structural features make it a valuable candidate for drug discovery, particularly in targeting enzymes and receptors involved in metabolic pathways.
The growing interest in heterocyclic compounds like N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride stems from their versatility in medicinal chemistry. Researchers are increasingly exploring its potential applications in developing antimicrobial agents and anti-inflammatory drugs, aligning with current trends in combating antibiotic resistance and chronic diseases. The compound’s chlorothiazole group enhances its binding affinity to biological targets, a property highly sought after in rational drug design.
From a synthetic perspective, CAS 1353964-90-5 exemplifies the importance of scaffold diversification in modern organic chemistry. Its cyclopropanamine segment introduces steric constraints that can modulate molecular conformation, influencing pharmacokinetic profiles. This aligns with frequent search queries such as "role of cyclopropylamine in drug design" and "thiazole derivatives in medicinal chemistry", reflecting the compound’s relevance to cutting-edge research.
In agrochemical applications, derivatives of N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride have shown promise as plant growth regulators and pest control agents. The chlorothiazolyl moiety’s electron-withdrawing properties contribute to its bioactivity, addressing industry demands for sustainable crop protection solutions—a topic frequently searched in connection with "green chemistry in agriculture".
Analytical studies of CAS 1353964-90-5 emphasize its stability under physiological conditions, with HPLC and LC-MS data confirming high purity standards. These characteristics answer common technical queries like "analytical methods for amine hydrochloride salts" while supporting its utility in high-throughput screening platforms. The compound’s solubility profile further enhances its applicability in formulation development.
Recent patent literature highlights innovative uses of N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride in kinase inhibitor design, particularly for oncology targets. This connects with trending searches on "next-generation cancer therapeutics", demonstrating how this molecular scaffold bridges academic research and industrial innovation. Computational modeling studies predict favorable ADMET properties for its derivatives.
Environmental considerations regarding chlorinated heterocycles have led to improved synthetic protocols for CAS 1353964-90-5, reducing hazardous byproducts. Such advancements respond to growing concerns about "green synthesis of pharmaceutical intermediates", making this compound a case study in sustainable chemical production.
The crystalline nature of N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride facilitates precise X-ray diffraction analysis, providing structural insights valuable for structure-activity relationship (SAR) studies. Researchers frequently investigate "crystallography of amine salts" to optimize molecular interactions, further underscoring this compound’s scientific significance.
As regulatory agencies emphasize quality by design (QbD) principles, the well-characterized properties of CAS 1353964-90-5 make it an exemplary subject for process chemistry optimization. This addresses industry searches for "scale-up strategies for complex amines" while ensuring reproducible synthetic outcomes.
In conclusion, N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride represents a multifaceted tool for researchers exploring bioactive small molecules. Its structural complexity and demonstrated applications across therapeutic and agricultural domains position it as a compound of enduring scientific and commercial interest.
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