CAS 98737-29-2
:(2S,3S)-(-)-3-tert-Butoxycarbonylamino-1,2-epoxy-4-phenylbutane
Description:
(2S,3S)-(-)-3-tert-Butoxycarbonylamino-1,2-epoxy-4-phenylbutane is a chiral compound characterized by its specific stereochemistry, indicated by the (2S,3S) configuration. This compound features a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in organic synthesis to protect amines during chemical reactions. The presence of an epoxy group in its structure suggests that it has potential reactivity, particularly in nucleophilic addition reactions. The phenyl group contributes to the compound's hydrophobic characteristics and can influence its solubility and interaction with biological systems. As a chiral molecule, it may exhibit different biological activities depending on its stereochemistry, making it of interest in pharmaceutical applications. The CAS number 98737-29-2 uniquely identifies this compound in chemical databases, facilitating its study and use in research and industry. Overall, this compound's unique structural features and stereochemistry make it a valuable entity in synthetic organic chemistry and medicinal chemistry.
Formula:C15H21NO3
InChI:InChI=1S/C15H21NO3/c1-15(2,3)19-14(17)16-12(13-10-18-13)9-11-7-5-4-6-8-11/h4-8,12-13H,9-10H2,1-3H3,(H,16,17)/t12-,13+/m0/s1
InChI key:InChIKey=NVPOUMXZERMIJK-QWHCGFSZSA-N
SMILES:[C@@H](CC1=CC=CC=C1)(NC(OC(C)(C)C)=O)[C@]2(CO2)[H]
Synonyms:- (1S,2S)-Boc epoxide
- (1S,2S)1,2-Epoxy-3-(Boc Amino)-4-Phenylbutane
- (2R)-[(1'S)-tert-butoxycarbonyl)amino-2'-phenyethyl]-oxirane
- (2S)-[(1S)-1-[(tert-Butoxycarbonyl)amino]-2-phenylethyl]oxirane
- (2S,3S)-(-)-3-tert-Butoxycarbonylamino-1,2-epoxy-4-phenylbutane
- (2S,3S)-1,2-Epoxy-3-(Boc-Amino)-4-Phenylbutane
- (2S,3S)-3-(tert-Butoxycarbonyl)amino-1,2-epoxy-4-phenylbutane
- (2S,3S)-N-t-Boc-3-amino-1,2-epoxy-4-phenylbutane
- 1,2-Epoxy-(BOC amino)-4-phenyl butane
- 1-Benzyl-2,3-Epoxypropyl-Carbamic Acid Tert-Butyl Ester
- Boc-expoxide-4-phenylbutane
- Carbamic acid, (1-oxiranyl-2-phenylethyl)-, 1,1-dimethylethyl ester, [S-(R*,R*)]-
- Carbamic acid, N-[(1S)-1-[(2S)-2-oxiranyl]-2-phenylethyl]-, 1,1-dimethylethyl ester
- Carbamic acid, [(1S)-1-(2S)-oxiranyl-2-phenylethyl]-, 1,1-dimethylethyl este
- Carbamic acid, [(1S)-1-(2S)-oxiranyl-2-phenylethyl]-, 1,1-dimethylethyl ester
- Tert-Butyl (1-Oxiran-2-Yl-2-Phenylethyl)Carbamate
- Tert-Butyl{(S)-Α-[(S)-Oxiranyl]Phenethyl}Carbamate
- [(1S)-1-((2S)-Oxiranyl)-2-phenylethyl]carbamic acid tert-butyl ester
- tert-Butyl N-[(1S)-1-[(2S)-oxiran-2-yl]-2-phenylethyl]carbamate
- tert-Butyl [(1S)-1-((2S)-oxiranyl)-2-phenylethyl]carbamate
- tert-butyl {(1S)-1-[(2R)-oxiran-2-yl]-2-phenylethyl}carbamate
- See more synonyms
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Found 12 products.
(2S,3S)-(-)-3-(t-BOC-amino)-1,2-Epoxy-4-phenylbutane
CAS:Formula:C15H21NO3Purity:98%Color and Shape:SolidMolecular weight:263.3321(2S,3S)-1,2-Epoxy-3-(Boc-Amino)-4-Phenylbutane
CAS:(2S,3S)-1,2-Epoxy-3-(Boc-Amino)-4-PhenylbutanePurity:98%Molecular weight:263.33g/moltert-Butyl ((S)-(R ,R ))-(-)-(1-oxiranyl-2-phenylethyl)carbamate
CAS:Formula:C15H21NO3Molecular weight:263.34(2S,3S)-3-(tert-Butoxycarbonylamino)-1,2-epoxy-4-phenylbutane
CAS:Formula:C15H21NO3Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:263.34(2S,3S)-N-t-Boc-3-amino-1,2-epoxy-4-phenylbutane
CAS:Formula:C15H21NO3Purity:95%Color and Shape:SolidMolecular weight:263.337(2S,3S)-3-Boc-amino-1,2-epoxy-4-phenylbutane
CAS:Controlled Product<p>Applications Atazanavir intermediate. Enantiomer S.<br>References Vassar, R., et al.: Science, 286, 735 (1999), Maillard, M., et al.: J. Med. Chem., 50, 776 (2007), Stauffer, S., et al.: Bioorg. Med. Chem. Lett., 17, 1788 (2007),<br></p>Formula:C15H21NO3Color and Shape:NeatMolecular weight:263.33(2S,3S)-3-Boc-amino-1,2-epoxy-4-phenylbutane
CAS:<p>(2S,3S)-3-Boc-amino-1,2-epoxy-4-phenylbutane is a potent and selective inhibitor of HIV protease. It binds to the active site of the enzyme and prevents the formation of an enzyme-substrate complex, which inhibits protein synthesis. (2S,3S)-3-Boc-amino-1,2-epoxy-4-phenylbutane has been shown to be a potent inhibitor for other serine proteases such as chymotrypsin and trypsin. This compound has also been shown to be effective in inhibiting a number of proteases from bacteria such as Bacillus subtilis and Pseudomonas aeruginosa. Inhibitors have also been found against nonenzymatic protein inhibitors such as bacitracin, polymyxin B, colistin sulfate, vancomycin, and daptomycin</p>Formula:C15H21NO3Purity:Min. 95%Color and Shape:PowderMolecular weight:263.33 g/mol(2S,3S)-N-t-Boc-3-amino-1,2-epoxy-4-phenylbutane
CAS:<p>(2S,3S)-N-t-Boc-3-amino-1,2-epoxy-4-phenylbutane is a useful organic compound for research related to life sciences. The catalog number is T66307 and the CAS number is 98737-29-2.</p>Formula:C15H21NO3Color and Shape:SolidMolecular weight:263.337
![tert-Butyl N-[(1S)-1-((2S)-Oxiran-2-yl)-2-phenylethyl]carbamate](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F86%2Fthumb%2FMM3624.07-0025.jpg&w=3840&q=75)
