CAS 58737-22-7
:P-aminophenyl-1-thio-beta-D-*glucopyranoside
Description:
P-aminophenyl-1-thio-beta-D-glucopyranoside is a chemical compound characterized by its structure, which includes a glucopyranoside moiety linked to a thioether and an amino group. This compound features a phenyl group substituted with an amino group (–NH2) at the para position, which contributes to its reactivity and potential biological activity. The thioether linkage imparts unique properties, enhancing solubility and stability in various solvents. P-aminophenyl-1-thio-beta-D-glucopyranoside is often utilized in biochemical applications, particularly in the synthesis of glycosides and as a substrate in enzymatic assays. Its ability to participate in nucleophilic substitution reactions makes it valuable in organic synthesis. Additionally, the presence of the amino group allows for further functionalization, making it a versatile building block in medicinal chemistry and research. Safety data should be consulted for handling, as with any chemical, to ensure proper precautions are taken during use.
Formula:C12H17NO5S
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Found 4 products.
4-Aminophenyl b-D-thioglucopyranoside
CAS:Formula:C12H17NO5SPurity:≥ 98%Color and Shape:Light-yellow solidMolecular weight:287.334-Aminophenyl 1-thio-β-D-glucopyranoside
CAS:4-Aminophenyl 1-thio-β-D-glucopyranosideMolecular weight:287.33208g/mol4-Aminophenyl 1-Thio-β-D-glucopyranoside
CAS:Controlled Product<p>Applications 4-Aminophenyl 1-Thio-β-D-glucopyranoside is a glycoside derivative of 4-Amino-benzenethiol (A591510); a compound used in the preparation of CCR5 antagonists as anti-HIV-1 agents. It can also be used to synthesize functionalized Coumarins (C755380) as acetylcholinesterase inhibitors.<br>References Seto, M., et al.: Bioorg. Med. Chem., 13, 363 (2004); Shen, Q., et al.: Eur. J. Med. Chem., 40, 1307 (2005)<br></p>Formula:C12H17NO5SColor and Shape:NeatMolecular weight:287.3324-Aminophenyl b-D-thioglucopyranoside
CAS:<p>4-Aminophenyl b-D-thioglucopyranoside is a compound that belongs to the group of small molecules and has been studied for its potential use as a drug to treat brain tumours. It has been shown that 4-Aminophenyl b-D-thioglucopyranoside binds to centromeric DNA sequences in mammalian cells, which can lead to inhibition of transcription and replication. This inhibitory effect on transcription and replication is due to the inhibition of acetyltransferase enzymes by 4-Aminophenyl b-D-thioglucopyranoside.</p>Formula:C12H17NO5SPurity:Min. 95%Molecular weight:287.33 g/mol



