CAS 98737-29-2

(2S,3S)-(-)-3-terc-butiloxicarbonilamino-1,2-epoxi-4-fenilbutano

Descrição:

(2S,3S)-(-)-3-terc-butiloxicarbonilamino-1,2-epoxi-4-fenilbutano é um composto quiral caracterizado por sua estereoquímica específica, indicada pela configuração (2S,3S). Este composto apresenta um grupo protetor tert-butiloxicarbonila (Boc), que é comumente usado na síntese orgânica para proteger aminas durante reações químicas. A presença de um grupo epóxido em sua estrutura sugere que ele tem reatividade potencial, particularmente em reações de adição nucleofílica. O grupo fenila contribui para as características hidrofóbicas do composto e pode influenciar sua solubilidade e interação com sistemas biológicos. Como uma molécula quiral, pode apresentar diferentes atividades biológicas dependendo de sua estereoquímica, tornando-a de interesse em aplicações farmacêuticas. O número CAS 98737-29-2 identifica exclusivamente este composto em bancos de dados químicos, facilitando seu estudo e uso em pesquisa e indústria. No geral, as características estruturais únicas e a estereoquímica deste composto o tornam uma entidade valiosa na química orgânica sintética e na química medicinal.

Fórmula: 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

Chave InChI: InChIKey=NVPOUMXZERMIJK-QWHCGFSZSA-N

SMILES: [C@@H](CC1=CC=CC=C1)(NC(OC(C)(C)C)=O)[C@]2(CO2)[H]

Sinónimos:

• (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

(2S,3S)-(-)-3-(t-BOC-amino)-1,2-Epoxy-4-phenylbutane

CAS: 98737-29-2

Fórmula: C₁₅H₂₁NO₃

Pureza: 98%

Cor e Forma: Solid

Peso molecular: 263.3321

Ref: IN-DA0039MJ

(2S,3S)-1,2-Epoxy-3-(Boc-Amino)-4-Phenylbutane

CAS: 98737-29-2

(2S,3S)-1,2-Epoxy-3-(Boc-Amino)-4-Phenylbutane

Pureza: 98%

Peso molecular: 263.33g/mol

Ref: 54-OR1008023

tert-Butyl ((S)-(R ,R ))-(-)-(1-oxiranyl-2-phenylethyl)carbamate

CAS: 98737-29-2

Fórmula: C₁₅H₂₁NO₃

Peso molecular: 263.34

Ref: 7W-GK6607

(2S,3S)-3-(tert-Butoxycarbonylamino)-1,2-epoxy-4-phenylbutane

CAS: 98737-29-2

Fórmula: C₁₅H₂₁NO₃

Pureza: >98.0%(GC)

Cor e Forma: White to Almost white powder to crystal

Peso molecular: 263.34

Ref: 3B-E0893

tert-Butyl N-[(1S)-1-((2S)-Oxiran-2-yl)-2-phenylethyl]carbamate

CAS: 98737-29-2

Cor e Forma: Neat

Ref: 86-MM3624.07

Atazanavir Impurity 21

CAS: 98737-29-2

Fórmula: C₁₅H₂₁NO₃

Peso molecular: 263.34

Ref: 4Z-A-7737

Darunavir Impurity 22

CAS: 98737-29-2

Fórmula: C₁₅H₂₁NO₃

Peso molecular: 263.33

Ref: ST-EA-CP-D70004

(2S,3S)-N-t-Boc-3-amino-1,2-epoxy-4-phenylbutane

CAS: 98737-29-2

Fórmula: C₁₅H₂₁NO₃

Pureza: 95%

Cor e Forma: Solid

Peso molecular: 263.337

Ref: 10-F076757

(2S,3S)-3-Boc-amino-1,2-epoxy-4-phenylbutane

Produto Controlado

CAS: 98737-29-2

Applications Atazanavir intermediate. Enantiomer S.
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),

Fórmula: C₁₅H₂₁NO₃

Cor e Forma: Neat

Peso molecular: 263.33

Ref: TR-B618530

(2S,3S)-3-Boc-amino-1,2-epoxy-4-phenylbutane

CAS: 98737-29-2

(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

Fórmula: C₁₅H₂₁NO₃

Pureza: Min. 95%

Cor e Forma: Powder

Peso molecular: 263.33 g/mol

Ref: 3D-FB18916

Atazanavir Impurity 21

CAS: 98737-29-2

Fórmula: C₁₅H₂₁NO₃

Peso molecular: 263.34

Ref: ST-EA-CP-A28070

(2S,3S)-N-t-Boc-3-amino-1,2-epoxy-4-phenylbutane

CAS: 98737-29-2

(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.

Fórmula: C₁₅H₂₁NO₃

Cor e Forma: Solid

Peso molecular: 263.337

Ref: TM-T66307