CAS 98760-08-8

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

Descrição:

A substância química conhecida como (2R,3S)-3-(tert-butiloxicarbonilamino)-1,2-epoxi-4-fenilbutano, com o número CAS 98760-08-8, é um composto orgânico caracterizado por seus grupos funcionais epóxido e amina. Este composto apresenta um centro quiral, que contribui para sua estereoquímica, especificamente a configuração (2R,3S). A presença do grupo tert-butoicocarbonila (Boc) indica que provavelmente é utilizado na síntese de peptídeos ou como grupo protetor para aminas na síntese orgânica. O grupo epóxido fornece reatividade que pode ser explorada em várias transformações químicas, tornando-se um intermediário versátil na química orgânica. Além disso, o grupo fenila ligado à cadeia de butano pode influenciar as propriedades físicas do composto, como solubilidade e estabilidade. No geral, este composto é de interesse na química orgânica sintética, particularmente no desenvolvimento de fármacos e moléculas biologicamente ativas. Suas características específicas, incluindo ponto de fusão, ponto de ebulição e solubilidade, precisariam ser determinadas experimentalmente ou obtidas de bancos de dados químicos confiáveis.

Fórmula: C₁₅H₂₁NO₃

InChI: InChI=1/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-STQMWFEESA-N

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

Sinónimos:

• (1S,2R)-Boc epoxide
• (2R,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane
• (2R,3S)-3-(Tert-Butoxycarbonyl)Amino-1,2-Epoxy-4-Phenylbutane
• (2R,3S)-3-(tert-ButoxycarbonyI)amino-1,2-epoxy-4-phenylbutane
• (2R,3S)-3-(tert-Butoxycarbonyl)amino-1,2-epoxy-4-phenylbutane,Carbamic acid, N-[(1S)-1-(2R)-2-oxiranyl-2-phenylethyl]-, 1,1-dimethylethyl ester
• (2R,3S)-3-(tert-Butoxycarbonylamino)-1,2-epoxy-4-phenylbutane
• (2R,3S)-3-(tert-Butoxy  carbonyl)amino-1,2-epoxy-4-phenylbutane
• (2R,3S)-N-BOC-3-amino-1,2-epoxy-4-phenylbutane
• (2R,3S)-N-Boc-3-amino-1,2-epoxy-4-Phenylbutane (Boc Epoxy)
• Boc Epoxy
• Carbamic acid, (1-oxiranyl-2-phenylethyl)-, 1,1-dimethylethyl ester, [R-(R*,S*)]-
• Carbamic acid, N-[(1S)-1-(2R)-2-oxiranyl-2-phenylethyl]-, 1,1-dimethylethyl ester
• Carbamic acid, [(1S)-1-(2R)-oxiranyl-2-phenylethyl]-, 1,1-dimethylethyl ester
• Carbamic acid, [(1S)-1-(2R)-oxiranyl-2-phenylethyl]-, 1,1-dimethylethyl ester (9CI (2R,3S)-3-(tert-Butoxycarbonylamino)-1,2-epoxy-4-phenylbutane
• [(2S)-2-Phenyl-2-((2R)-oxiran-2-yl)ethyl]carbamic acid tert-butyl ester
• tert-Butyl N-[(1S)-1-((2R)-oxiran-2-yl)-2-phenylethyl]carbamate
• tert-Butyl [(1S)-1-[(2R)-oxiranyl]2-phenylethyl]carbamate
• tert-butyl [(1S)-1-(oxiran-2-yl)-2-phenylethyl]carbamate
• TERT-BUTYL (1S)-1-[(2R)-OXIRAN-2-YL]-2-PHENYLETHYLCARBAMATE
• tert-Butyl[(1S,2R)-oxiranyl-2-phenylethyl]carbamate
• [(1S)-1-((2R)-Oxiranyl)-2-phenylethyl]carbamic Acid tert-Butyl Ester
• THREO-N-BOC-L-PHENYLALANINE EPOXIDE
• (RS) BOC EPOXIDE // 2,R-3S,-3-N-TERT-BUT
• N-[(1S)-1-[(2R)-2-Oxiranyl]-2-phenylethyl]-carbamic Acid 1,1-Dimethylethyl Ester
• (2R,3S)-1,2-Epoxy-3-N-(tert-butoxycarbonyl)amino-
• (2R,3S)-3-(tert-Boc)amino-1,2-epoxy-4-phenylbutane
• (2r,3s)-3-(n-boc-amino)-1-oxirane-4-phenylbutane
• TERT-BUTYL (S)-1-((R)-OXIRAN-2-YL)-2-PHENYLETHYLCARBAMATE
• (2R, 3S)-1,2-EPOXY-3-N-(TERT-BUTOXYCARBONYL)AMINO-4-PHENYLBUTANE

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

CAS: 98760-08-8

Fórmula: C₁₅H₂₁NO₃

Pureza: 97%

Cor e Forma: Solid

Peso molecular: 263.3321

Ref: IN-DA0032C9

Atazanavir Impurity 17

CAS: 98760-08-8

Fórmula: C₁₅H₂₁NO₃

Cor e Forma: White To Off-White Solid

Peso molecular: 263.34

Ref: 4Z-A-7722

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

CAS: 98760-08-8

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

Pureza: 98%

Peso molecular: 263.33g/mol

Ref: 54-OR350336

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

Produto Controlado

CAS: 98760-08-8

Impurity Atazanavir Impurity C
Applications Atazanavir intermediate. Enantiomer R. Atazanavir Impurity C
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-B618531

(2R,3S)-3-(tert-Butoxycarbonyl)amino-1,2-epoxy-4-phenylbutane

CAS: 98760-08-8

The compound (2R,3S)-3-(tert-Butoxycarbonyl)amino-1,2-epoxy-4-phenylbutane is an epoxide with a thionyl chloride mediated reaction. This compound has been shown to react with amines and nucleophiles to form epoxides. The time required for this reaction was found to be dependent on the concentration of the amine. The reaction was also found to be chiral as it produced a mixture of diastereomers. When irradiated, this compound undergoes a stereoselective reaction that leads to a new epoxide product.

Fórmula: C₁₅H₂₁NO₃

Pureza: Min. 95%

Cor e Forma: Off-White Powder

Peso molecular: 263.34 g/mol

Ref: 3D-FB07938

(2R,3S)-3-(tert-Butoxycarbonyl)amino-1,2-epoxy-4-phenylbutane

CAS: 98760-08-8

Fórmula: C₁₅H₂₁NO₃

Pureza: 97%

Cor e Forma: Solid, White powder

Peso molecular: 263.337

Ref: 10-F212369

Atazanavir Impurity C

CAS: 98760-08-8

Fórmula: C₁₅H₂₁NO₃

Peso molecular: 263.33

Ref: ST-EA-CP-A28019