CAS 671212-34-3
:tert-butyl [2-(4-benzylpiperazin-1-yl)-2-oxoethyl]carbamate
Description:
Tert-butyl [2-(4-benzylpiperazin-1-yl)-2-oxoethyl]carbamate, identified by its CAS number 671212-34-3, is a chemical compound characterized by its unique structure, which includes a tert-butyl group, a piperazine moiety, and a carbamate functional group. This compound typically exhibits properties associated with both organic amines and carbamates, such as moderate solubility in organic solvents and potential reactivity with nucleophiles due to the presence of the carbamate linkage. The piperazine ring contributes to its biological activity, often enhancing interactions with biological targets, making it of interest in medicinal chemistry. The presence of the benzyl group may also influence its lipophilicity and overall pharmacokinetic properties. As with many organic compounds, its stability can be affected by environmental factors such as temperature and pH. Overall, this compound's characteristics make it a subject of interest for research in drug development and related fields.
Formula:C18H27N3O3
InChI:InChI=1/C18H27N3O3/c1-18(2,3)24-17(23)19-13-16(22)21-11-9-20(10-12-21)14-15-7-5-4-6-8-15/h4-8H,9-14H2,1-3H3,(H,19,23)
SMILES:CC(C)(C)OC(=NCC(=O)N1CCN(CC1)Cc1ccccc1)O
Synonyms:- 4-Benzyl-1-(Boc-amino-acetyl)-piperazine
- Carbamic acid,N-[2-oxo-2-[4-(phenylmethyl)-1-piperazinyl]ethyl]-, 1,1-dimethylethyl ester
- (2-[4-Benzyl-piperazin-1-yl]-2-oxo-ethyl)-carbamicacid tert-butyl ester
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Found 3 products.
tert-Butyl N-[2-(4-benzylpiperazin-1-yl)-2-oxoethyl]carbamate
CAS:<p>tert-Butyl N-[2-(4-benzylpiperazin-1-yl)-2-oxoethyl]carbamate</p>Molecular weight:333.42528g/mol(2-[4-Benzyl-piperazin-1-yl]-2-oxo-ethyl)-carbamic acid tert-butyl ester
CAS:Formula:C18H27N3O3Molecular weight:333.4324-Benzyl-1-(Boc-amino-acetyl)-piperazine
CAS:Controlled Product<p>4-Benzyl-1-(Boc-amino-acetyl)-piperazine is an industrial preparation that is used as a synthetic intermediate. It is a hexanoic acid ester of 4-benzyl piperazine. The compound was synthesized by reacting hexanoic acid with Boc-protected aminoacetic acid in the presence of triethylamine, trimethyl orthoformate, and tert-butyl alcohol. 4-Benzyl-1-(Boc-amino-acetyl)-piperazine was obtained as a white solid.</p>Formula:C18H27N3O3Purity:Min. 95%Molecular weight:333.4 g/mol



