Identification | Back Directory | [Name]
BOC-D-HIS-OH | [CAS]
50654-94-9 | [Synonyms]
BOC-D-HIS-OH BOC-D-HISTIDINE N-α-Boc-D-histidine N(a)-Boc-D-histidine n(à)-boc-d-histidine Boc-D- histidine acid N-ALPHA-BOC-D-HISTIDINE N-ALPHA-T-BOC-D-HISTIDINE N(ɑ)-Boc-D-histidine, 98+% Boc-D-His-OH >=98.0% (TLC) N(^a)-Boc-D-histidine, 98+% Nα-Boc-D-histidine N(alpha)-Boc-D-histidine, 98+% n(à)-tert-butoxycarbonyl-d-histidine N-ALPHA-T-BUTOXYCARBONYL-D-HISTIDINE N-ALPHA-T-BUTYLOXYCARBONYL-D-HISTIDINE NALPHA-(TERT-BUTOXYCARBONYL)-D-HISTIDIN NALPHA-(TERT-BUTOXYCARBONYL)-D-HISTIDINE N-ALPHA-TERT-BUTYLOXYCARBONYL-D-HISTIDINE (2R)-2-(tert-butoxycarbonylamino)-3-(3H-imidazol-4-yl)propanoic acid (2R)-2-(tert-butoxycarbonylamino)-3-(3H-imidazol-4-yl)propionic acid (R)-2-((tert-butoxycarbonyl)aMino)-3-(1H-iMidazol-4-yl)propanoic acid (R)-2-((tert-Butoxycarbonyl)amino)-3-(1H-imidazol-4-yl)propionic acid (2R)-2-{[(tert-butoxy)carbonyl]aMino}-3-(1H-iMidazol-4-yl)propanoic acid (2R)-2-[(tert-butoxy-oxomethyl)amino]-3-(3H-imidazol-4-yl)propanoic acid (2R)-3-(3H-imidazol-4-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid | [Molecular Formula]
C11H17N3O4 | [MDL Number]
MFCD00037851 | [MOL File]
50654-94-9.mol | [Molecular Weight]
255.27 |
Chemical Properties | Back Directory | [Appearance]
white powder | [Melting point ]
193-197 °C
| [Boiling point ]
398.5°C (rough estimate) | [density ]
1.275 | [refractive index ]
1.5700 (estimate) | [storage temp. ]
Store at 0-5°C | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
3.37±0.10(Predicted) | [color ]
White to Off-White | [BRN ]
4196575 | [CAS DataBase Reference]
50654-94-9 |
Hazard Information | Back Directory | [Chemical Properties]
white powder | [Uses]
Nα-Boc-D-histidine is an N-Boc-protected form of D-Histidine (H456015). D-Histidine is the unnatural, biologically inactive isomer of L-Histidine (H456010). D-histidine is known to inhibit cell division, and is also used by certain types of bacteria (such as Escherichia coli) as a source of L-Histidine. | [reaction suitability]
reaction type: Boc solid-phase peptide synthesis | [storage]
Store at -20°C |
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