77390-81-9

Usage

Uses

Used in Organic Synthesis:
Benzyl [(2Z)-2-amino-2-iminoethyl]carbamate is utilized as a reagent in organic synthesis, playing a crucial role in the formation of various complex organic molecules. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medical Research:
In the field of medical research, benzyl [(2Z)-2-amino-2-iminoethyl]carbamate has been investigated for its potential therapeutic applications. Studies have explored its use in the treatment of diabetes, where it may help regulate blood sugar levels and improve insulin sensitivity. Additionally, its potential as an anticancer agent has been examined, with research focusing on its ability to target and inhibit the growth of cancer cells.
Used in Environmental Studies:
Benzyl [(2Z)-2-amino-2-iminoethyl]carbamate has also been implicated as a possible pollutant in environmental studies. Its detection in water and sediment samples has raised concerns about its potential impact on ecosystems and human health. As a result, it is used as a subject of study for understanding the extent of its presence in the environment, its sources, and the development of methods for its removal or mitigation.

Upstream product

• 1755-98-2 ethyl 2-phenylmethoxycarbonylaminoethanimidate 
• 77390-70-6 3,5-O-isopropylidene-2'-N-benzyloxycarbonylaminomethyl-α-D-xylofuranoso<1,2-d>-Δ^2'-oxazoline 
• 51030-44-5 ethyl 2-benzyloxycarbonylaminoacetimidate hydrochloride 
• 859918-98-2 2-benzyloxycarbonylamino-acetimidic acid cyclohexyl ester 
• 501-53-1 benzyl chloroformate 
• 52485-57-1 3,5-O-isopropylidene-D-xylofuranosylammonium p-toluenesulfonate 

Downstream Products

• 126232-02-8 7-[2-(Benzyloxycarbonylamino-methyl)-pyrimidin-4-yl]-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid 
• 1418131-84-6 benzyl [(4-oxo-4,5,7,8-tetrahydro-3H-pyrano[4,3-d]pyrimidin-2-yl)methyl]carbamate 
• 1060687-81-1 {2-[(3-chloro-pyrazine-2-carbonyl)-amino]-2-imino-ethyl}-carbamic acid benzyl ester 

Relevant academic research and scientific papers

Purines, Pyrimidines, and Imidazoles. Part 57. Reactions of Some Oxazolino-xylofuranose Derivatives

2'-Methyl-3,5-O-isopropylidene-α-D-xylofuranoso-Δ2'-oxazoline reacts with benzaldehyde, p-nitrobezaldehyde, and anisaldehyde to give 2'-styryl-, 2'-p-nitrostyryl-, or 2'-p-methoxystyryl-3,5-O-isopropylidene-α-D-xylofuranoso-Δ2'-oxazolines. 3,5-O-Isopropylidene-D-xylofuranosylamine with carbon disulphide gave 2'-mercapto-3,5-O-isopropylidene-α-Δ-xylofuranoso-Δ2'-oxazoline, methylation of which produced the 2'-methylthio-oxazoline, which was desulphurised to give 3,5-O-isopropylidene-α-D-xylofuranoso-Δ2'-oxazoline.The xylosylamine with p-tolylsulphonylaminoacetimidate and benzyloxycarbonylaminoacetimidate gave 2'-p-tolylsulphonylaminomethyl (or benzyloxycarbonylaminomethyl)-3,5-O-isopropylidene-α-D-xylofuranoso-Δ2'-oxazolines respectively.The tolylsulphonylaminomethyl-oxazoline with hydrogen sulphide gave 3,5-O-isopropylidene-N-(N-p-tolylsulphonylthioglycyl)-D-xylofuranosylamine which with methanesulphonyl chloride gave 3,5-O-isopropylidene-2'-(p-tolylsulphonylaminomethyl)-α-D-xylofuranoso-Δ2'-thiazoline.Reaction of the p-tolylsulphonylaminomethyl- or benzyloxycarbonylaminomethyl-oxazolines with hydroxylamine gave corresponding 3,5-O-isopropylidene-D-xylofuranosylamidoximes, whereas with ammonia the sugar unit was cleaved and simple glycinamidines obtained.The structures assigned were confirmed by analytical, u.v., n.m.r., and mass-spectral techniques.