CAS 98760-08-8

(2R,3S)-3-(tert-butilossicarbonilamino)-1,2-epossi-4-fenilbutano

Descrizione:

La sostanza chimica nota come (2R,3S)-3-(tert-butilossicarbonilamino)-1,2-epossi-4-fenilbutano, con il numero CAS 98760-08-8, è un composto organico caratterizzato dai suoi gruppi funzionali epossidico e amminico. Questo composto presenta un centro chirale, che contribuisce alla sua stereochimica, specificamente la configurazione (2R,3S). La presenza del gruppo tert-butoicocarbonile (Boc) indica che è probabilmente utilizzato nella sintesi di peptidi o come gruppo protettivo per ammine nella sintesi organica. Il gruppo epossido fornisce reattività che può essere sfruttata in varie trasformazioni chimiche, rendendolo un intermedio versatile nella chimica organica. Inoltre, il gruppo fenile attaccato alla catena di butano può influenzare le proprietà fisiche del composto, come solubilità e stabilità. In generale, questo composto è di interesse nella chimica organica sintetica, in particolare nello sviluppo di farmaci e molecole biologicamente attive. Le sue caratteristiche specifiche, inclusi punto di fusione, punto di ebollizione e solubilità, dovrebbero essere determinate sperimentalmente o reperite da database chimici affidabili.

Formula: 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

InChI key: InChIKey=NVPOUMXZERMIJK-STQMWFEESA-N

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

Sinonimi:

• (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

Formula: C₁₅H₂₁NO₃

Purezza: 97%

Colore e forma: Solid

Peso molecolare: 263.3321

Ref: IN-DA0032C9

Atazanavir Impurity 17

CAS: 98760-08-8

Formula: C₁₅H₂₁NO₃

Colore e forma: White To Off-White Solid

Peso molecolare: 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

Purezza: 98%

Peso molecolare: 263.33g/mol

Ref: 54-OR350336

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

Prodotto controllato

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),

Formula: C₁₅H₂₁NO₃

Colore e forma: Neat

Peso molecolare: 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.

Formula: C₁₅H₂₁NO₃

Purezza: Min. 95%

Colore e forma: Off-White Powder

Peso molecolare: 263.34 g/mol

Ref: 3D-FB07938

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

CAS: 98760-08-8

Formula: C₁₅H₂₁NO₃

Purezza: 97%

Colore e forma: Solid, White powder

Peso molecolare: 263.337

Ref: 10-F212369

Atazanavir Impurity C

CAS: 98760-08-8

Formula: C₁₅H₂₁NO₃

Peso molecolare: 263.33

Ref: ST-EA-CP-A28019