About (2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane
(2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane Synonym: tert-Butyl [S-(R*,R*)]-()-(1-oxiranyl-2-phenylethyl)carbamate Empirical Formula (Hill Notation): C15H21NO3Molecular Weight: 263.33CAS Number: 98737-29-2 assay 99% optical activity []23/D 7, c =0.6 in methanol mp 125-127C(lit.) Description Application Building block employed in the synthesis of HIV-1 protease inhibitors.[2][1] Employed in synthesizing (hydroxyethyl)urea peptidomimetrics[3] and arylsulfonamides possessing anti-HIV activity.[4] Packaging 1, 5 g in glass bottle
FAQs of (2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane:
Q: What is the molecular formula of (2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane?
A: The molecular formula of (2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane is C15H21NO3.
Q: What is the molecular weight of this product?
A: The molecular weight of (2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane is 263.33 grams (g).
Q: What is the purity of (2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane?
A: The purity of this product is 97%.
Q: What is the chemical structure classification of this compound?
A: (2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane contains an epoxy group, a Boc-protected amino group, and a phenyl ring.
Q: Is (2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane chiral?
A: Yes, this compound is chiral as it has two stereogenic centers at positions 2 and 3 in its structure.