| Identification | Back Directory | [Name]
BOC-D-DAP(Z)-OH DCHA | [CAS]
81306-94-7 | [Synonyms]
BOC-D-DAP(Z)-OH DCHA
BOC-D-DAP(Z)-OH DCHA USP/EP/BP
(Tert-Butoxy)Carbonyl D-Dap(Z)-OH·DCHA
N-α-Boc-N-β-Z-D-2,3-diaminopropionic acid dicycl
BOC-D-ALPHA,BETA-DIAMINOPROPIONIC ACID(Z)-OH DCHA
N2-Boc-N3-Cbz-D-2,3-diaminopropionic acid dicyclohexylamine
N-Boc-N'-Cbz-D-2,3-diaminopropionic acid dicyclohexylamine salt
N-α-Boc-N-β-Z-D-2,3-diaminopropionic acid dicyclohexylamine salt
N2-BOC-N3-CBZ-D-2,3-DIAMINOPROPIONIC ACID DICYCLOHEXYLAMINE SALT
Nα-Boc-Nβ-Z-D-2,3-diaminopropionic acid dicyclohexylammonium salt
Nα-Boc-Nβ-Z-D-2,3-diaminopropionic acid dicyclohexylammonium salt
BOC-N-BETA-Z-D-2,3-DIAMINOPROPIONIC ACID DICYCLOHEXYLAMMONIUM SALT
Nα-Boc-Nβ-Z-D-2,3-diaminopropionic acid dicyclohexylammonium salt99%
N-alpha-Boc-N-beta-Z-D-2,3-diaminopropionic acid dicyclohexylamine salt
dicyclohexylamine 3-(benzyloxycarbonylamino)-2-(tert-butoxycarbonylamino)propanoate
Boc-D-Dap(Z)-OH·DCHA(Na-Boc-N3-Z-D-2,3-DiaMinopropionic acid dicyclohexylaMine salt )
Boc-D-Dap(Z)-OH·DCHA N-α-Boc-N-β-Z-D-2,3-diaMinopropionic acid dicyclohexylaMine salt
Dicyclohexylamine (R)-3-(((benzyloxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)propanoate
N-ALPHA-T-BUTYLOXYCARBONYL-N-BETA-BENZYLOXYCARBONYL-D-2,3-DIAMINOPROPIONIC ACID DICYCLOHEXYLAMINE
N-ALPHA-TERT-BUTYLOXYCARBONYL-N-BETA-BENZYLOXYCARBONYL-D-2,3-DIAMINOPROPIONIC ACID DICYCLOHEXYLAMINE
N-[(1,1-Dimethylethoxy)carbonyl]-3-[[(phenylmethoxy)carbonyl]amino]-D-alanine dicyclohexylamine salt
N-ALPHA-T-BUTOXYCARBONYL-N-BETA-CARBOBENZOXY-D-ALPHA,BETA-DIAMONOPROPIONIC ACID DICYCLOHEXYLAMMONIUM SALT
N-cyclohexylcyclohexanamine,2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-(phenylmethoxycarbonylamino)propanoicaci
N-cyclohexylcyclohexanamine,2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-(phenylmethoxycarbonylamino)propanoic acid | [Molecular Formula]
C28H45N3O6 | [MDL Number]
MFCD00798629 | [MOL File]
81306-94-7.mol | [Molecular Weight]
519.68 |
| Hazard Information | Back Directory | [Uses]
Boc-d-dap(z)-oh DCHA was a useful reagent in preparation of amino acid-related diamines as modulators of chemokine receptor activity. |
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