CAS 98760-08-8

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

Description:

The chemical substance known as (2R,3S)-3-(tert-Butoxycarbonylamino)-1,2-epoxy-4-phenylbutane, with the CAS number 98760-08-8, is an organic compound characterized by its epoxy and amine functional groups. This compound features a chiral center, which contributes to its stereochemistry, specifically the (2R,3S) configuration. The presence of the tert-butoxycarbonyl (Boc) group indicates that it is likely used in peptide synthesis or as a protecting group for amines in organic synthesis. The epoxy group provides reactivity that can be exploited in various chemical transformations, making it a versatile intermediate in organic chemistry. Additionally, the phenyl group attached to the butane backbone can influence the compound's physical properties, such as solubility and stability. Overall, this compound is of interest in synthetic organic chemistry, particularly in the development of pharmaceuticals and biologically active molecules. Its specific characteristics, including melting point, boiling point, and solubility, would need to be determined experimentally or sourced from reliable chemical databases.

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]

Synonyms:

• (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

Purity: 97%

Color and Shape: Solid

Molecular weight: 263.3321

Ref: IN-DA0032C9

Atazanavir Impurity 17

CAS: 98760-08-8

Formula: C₁₅H₂₁NO₃

Color and Shape: White To Off-White Solid

Molecular weight: 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

Purity: 98%

Molecular weight: 263.33g/mol

Ref: 54-OR350336

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

Controlled Product

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

Color and Shape: Neat

Molecular weight: 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

Purity: Min. 95%

Color and Shape: Off-White Powder

Molecular weight: 263.34 g/mol

Ref: 3D-FB07938

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

CAS: 98760-08-8

Formula: C₁₅H₂₁NO₃

Purity: 97%

Color and Shape: Solid, White powder

Molecular weight: 263.337

Ref: 10-F212369

Atazanavir Impurity C

CAS: 98760-08-8

Formula: C₁₅H₂₁NO₃

Molecular weight: 263.33

Ref: ST-EA-CP-A28019