| Name： | BOC-DAP-OH |
| CAS： | 159002-17-2 ;76387-70-7 ;73259-81-1 |
| Synonyms： | N-BOC-L-2,3-DIAMINOPROPANOIC ACID ; BOC-DAP-OH ; NALPHA-BOC-L-BETA-AMINOALANINE ; (S)-3-AMINO-2-(TERT-BUTOXYCARBONYLAMINO)PROPIONIC ACID ; N-ALPHA-(T-BUTOXYCARBONYL)-L-ALPHA,BETA-DIAMINOPROPIONIC ACID ; BOC-D-DAP-OH ; (2S)-3-AMINO-2-([(TERT-BUTOXY)CARBONYL]AMINO)PROPANOIC ACID ; BOC-DAP ; T-BUTYLOXYCARBONYL-L-2,3-DIAMINOPROPIONIC ACID ; (S)-3-AMINO-2-(TERT-BUTOXYCARBONYLAMINO)PROPANOIC ACID ; 3-AMINO-N-BOC-L-ALANINE ; NALPHA-BOC-BETA-AMINO-L-ALANINE ; NALPHA-BOC-(S)-BETA-AMINOALANINE ; N-ALPHA-BOC-L-2,3-DIAMINOPROPIONIC ACID ; BOC-L-ALPHA,BETA-DIAMINOPROPIONIC ACID ; A-N-TERT-BUTOXYCARBONYL-B-AMINO-L-ALANINE ; N-A-BOC-L-2,3-DIAMINOPROPIONIC ACID ; (S)-2-[(TERT-BUTOXYCARBONYL)AMINO]-3-AMINOPROPIONIC ACID ; BOC-DAPA-OH ; NALPHA-BOC-2,3-DIAMINOPROPIONIC ACID ; BOC-L-DAPA-OH ; 3-AMINO-BOC-L-ALANINE ; NA-BOC-(S)-2,3-DIAMINOPROPIONIC ACID ; 3-AMINO-(TERT-BUTOXYCARBONYL)-L-ALANINE ; 3-AMINO-2-TERT-BUTOXYCARBONYLAMINO-PROPIONIC ACID ; N2-TERT-BUTOXYCARBONYL-L-2,3-DIAMINOPROPIONIC ACID ; N-ALPHA-BOC-L-DIAMINOPROPIONIC ACID ; N-ALPHA-L-(BUTOXYCARBONYL)-2,3-DIAMINOPROPIONIC ACID ; N-T-BOC-BETA-AMINO-L-ALANINE ; BOC-L-2,3-DIAMINOPROPIONIC ACID ; BOC-DPR-OH ; BOC-L-DAP-OH ; N-ALPHA-BOC-(S)-2,3-DIAMINOPROPIONIC ACID ; N2-(TERT-BUTOXYCARBONYL)-(S)-2,3-DIAMINOPROPIONIC ACID ; 3-AMINO-N-[(TERT-BUTOXY)CARBONYL]ALANINE ; N-ALPHA-T-BUTYLOXYCARBONYL-L-2,3-DIAMINOPROPIONIC ACID ; (N-BOC-BETA-AMINO)-ALA-OH ; N2-BOC-(2S)-2,3-DIAMINOPROPIONIC ACID |
| MDL.： | MFCD00236843 |
| H bond acceptor： | 6 |
| H bond donor： | 3 |
| Smile： | CC(C)(C)OC(=O)N[C@@H](CN)C(=O)O |
| InChi： | InChI=1S/C8H16N2O4/c1-8(2,3)14-7(13)10-5(4-9)6(11)12/h5H,4,9H2,1-3H3,(H,10,13)(H,11,12)/t5-/m0/s1 |
| InChiKey： | InChIKey=KRJLRVZLNABMAT-YFKPBYRVSA-N |
Property |
|
| Melting Point： | 210 DEG C (DEC)/210 °C |
| Comments： | APPLICATION: REACTANT FOR: PROTEIN ASSEMBLY DIRECTED BY SYNTHETIC MOLECULAR RECOGNITION MOTIFS. SOLID PHASE SYNTHESIS OF GRAMICIDIN S CYCLIC ANALOGS WITH ANTIBIOTIC AND HEMOLYTIC ACTIVITIES. SYNTHESIS OF HCV PROTEASE INHIBITOR MODIFIED ANALOGS. SOLID PHASE SYNTHESIS OF PEPTIDIC V1A RECEPTOR AGONISTS. DIRECTED PEPTIDE ASSEMBLY AT LIPID-WATER INTERFACE ASSAY METHOD: TLC IMPURITIES: APPROX 3% WATER OPTICAL ACTIVITY: [ALPHA]20/D +5.5+/-1 DEG, C = 1% IN METHANOL: WATER (1:1) OTHER NOTES: MONOPROTECTED DERIVATIVE OF DAP OTHER NOTES: USED EG IN THE SYNTHESIS OF GLUCOSAMINE SYNTHASE INHIBITORS, A MYOSIN KINASE INHIBITOR. PREPARATION OF PEPTIDES WITH METAL COMPLEXING GROUPS UNSPSC: 12352100 WGK: 3 |
Safety information |
|
| WGK Germany： | 3 |
BOC-DAP-OH
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