BOC-D-HIS-OH
Synonym(s):Nα-Boc-D -histidine
- CAS NO.:50654-94-9
- Empirical Formula: C11H17N3O4
- Molecular Weight: 255.27
- MDL number: MFCD00037851
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-06-29 22:56:24
What is BOC-D-HIS-OH?
Chemical properties
white powder
The Uses of BOC-D-HIS-OH
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.
Properties of BOC-D-HIS-OH
Melting point: | 193-197 °C |
Boiling point: | 398.5°C (rough estimate) |
Density | 1.275 |
refractive index | 1.5700 (estimate) |
storage temp. | Sealed in dry,2-8°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 |
Safety information for BOC-D-HIS-OH
Computed Descriptors for BOC-D-HIS-OH
New Products
(S)-3-Aminobutanenitrile hydrochloride 4-Methylphenylacetic acid N-Boc-D-alaninol N-BOC-D/L-ALANINOL Tert-butyl bis(2-chloroethyl)carbamate 3-Morpholino-1-(4-nitrophenyl)-5,6-dihydropyridin- 2(1H)-one Furan-2,5-Dicarboxylic Acid Tropic acid 1-Bromo-3,5-Di-Tert-Butylbenzene S-2-CHLORO PROPIONIC ACID ETHYL ISOCYANOACETATE 2-Bromo-1,3-Bis(Dimethylamino)Trimethinium Hexafluorophosphate 4-IODO BENZOIC ACID 3-NITRO-2-METHYL ANILINE 1-(2,4-DICHLOROPHENYL) ETHANAMINE (2-Hydroxyphenyl)acetonitrile 4-Bromopyrazole 2-(Cyanocyclohexyl)acetic acid 4-methoxy-3,5-dinitropyridine 1-(4-(aminomethyl)benzyl)urea hydrochloride 2-aminopropyl benzoate hydrochloride diethyl 2-(2-((tertbutoxycarbonyl)amino) ethyl)malonate tert-butyl 4- (ureidomethyl)benzylcarbamate Ethyl-2-chloro((4-methoxyphenyl)hydrazono)acetateRelated products of tetrahydrofuran
BOC-D-HIS-OH
N-Boc-1-phenylmethyl-D-histidine
BOC-D-HIS(BOC)-OH BENZENE
BOC-D-HIS(DNP)-OH IPOH
N-Boc-N'-tosyl-D-histidine
BOC-D-HIS(TRT)-OH
BOC-D-HIS(3-ME)-OH
BOC-D-HIS(TOS)-OH DCHA
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