91893-69-5

Basic information

• Product Name: 2-Amino-N,N-dimethylethane-1-sulfonamide hydrochloride
• Synonyms: 2-Amino-N,N-dimethylethane-1-sulfonamide hydrochloride
• CAS NO: 91893-69-5
• Molecular Formula: C4H13ClN2O2S
• Molecular Weight: 188.67622
• Mol File: 91893-69-5.mol
• Article Data: 5

Chemical Properties

• Melting Point: 144-146 °C
• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 2-Amino-N,N-dimethylethane-1-sulfonamide hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Amino-N,N-dimethylethane-1-sulfonamide hydrochloride(91893-69-5)
• EPA Substance Registry System: 2-Amino-N,N-dimethylethane-1-sulfonamide hydrochloride(91893-69-5)

Safety Data

• Hazardous Substances Data: 91893-69-5(Hazardous Substances Data)

Usage

Chemical compound

2-Amino-N,N-dimethylethane-1-sulfonamide hydrochloride
Commonly used as a pharmaceutical intermediate
Hydrochloride salt of the organic compound 2-Amino-N,N-dimethylethane-1-sulfonamide
Sulfonamide derivative
Used in synthesis of various pharmaceutical drugs
Acts as a building block in production of organic compounds
Studied for potential use as an antibacterial and antimicrobial agent
Investigated for potential use in synthesis of new materials
Used as a chemical reagent in organic chemistry reactions
Versatile chemical with potential applications in pharmaceutical and chemical industries

Upstream product

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Relevant articles and documents

Synthesis of 2-Aminoethanesulfonamides of Betulinic and Betulonic Acids

New potentially biologically active sulfonamide derivatives of pentacyclic lupane-type triterpenoids, the sulfonamide group of which was bonded to C-17 of the triterpene skeleton through an amidoethane spacer, were synthesized via conjugation of 2-aminoet

Synthesis and antiviral, insecticidal, and fungicidal activities of gossypol derivatives containing alkylimine, oxime or hydrazine moiety

Gossypol is a part of the cotton plant's defense system against pathogens and herbivorous insects. To discover gossypol analogs with broad spectrum and high activity, a series of gossypol alkylamine Schiff base, oxime and hydrazone derivatives were synthesised and bioassayed. The biological results indicated that most of these derivatives exhibited higher anti-TMV activity than gossypol. Interestingly, the activities of compounds 10, 15, 18, 20, 23 and 26 were much higher than that of ribavirin. Furthermore, compound 26, which was low toxicity to rat, showed better activity than control plant virus inhibitors in the field. Additionally, allyl amine Schiff base (9) displayed remarkable insecticidal activities against Mythimna separata, Helicoverpa armigera and Ostrinia nubilalis, whereas (pyridin-3-yl)methanamine Schiff base (13) showed excellent activity against Culex pipiens pallens. The fungicidal results revealed that all of compounds exhibited good activity against Physalospora piricola.

Carbapenem derivatives and a preparation method thereof

The present invention relates to carbapenem derivatives of Formula I, wherein X is carbonyl or sulfonyl, and a preparation method thereof. The carbapenem derivatives of the invention have excellent antibacterial properties and are thus useful as antibiotics.