Identification | Back Directory | [Name]
NW-09-15-1 | [CAS]
81323-58-2 | [Synonyms]
-(s) NW-09-15-1 BOC-HSE-OTBU BOC-Hser-OtBU N-Boc-L-hoMoserine Butyl Ester N-Boc-L-homoserine tert-butyl ester -tert-Butyl 2-((tert-butoxycarbonyl) N-t-Butyloxycarbonyl-L-hoMoserine-t-butyl ester tert-butyl (tert-butoxycarbonyl)-L-homoserinate (2S)-tert-butyl 2-[N-Boc-amino]-4-hydroxybutanoate N-(tert-butyloxycarbonyl)-(S)-homoserine tert-butyl ester (S)-tert-butyl 2-(tert-butoxycarbonylamino)-4-hydroxybutanoate 2(S)-2-tert-butoxycarbonylamino-4-hydroxybutyric acid tert-butyl ester L-Homoserine, N-[(1,1-dimethylethoxy)carbonyl]-, 1,1-dimethylethyl ester 2-Methyl-2-propanyl N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-hoMoserinate | [Molecular Formula]
C13H25NO5 | [MDL Number]
MFCD08275190 | [MOL File]
81323-58-2.mol | [Molecular Weight]
275.34 |
Chemical Properties | Back Directory | [Boiling point ]
393.4±37.0 °C(Predicted) | [density ]
1.071±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,2-8°C | [pka]
10.91±0.46(Predicted) |
Hazard Information | Back Directory | [Uses]
N-(tert-Butoxycarbonyl)-(S)-homoserine tert-Butyl Ester is used as a reactant in the synthesis of N-substituted sultam carboxylic acids as novel glycogen synthase activators. |
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