Boc-L-Histidine(Tosyl)
Synonym(s):Nα-Boc-N(im)-tosyl-L -histidine;Boc-His(Tos)-OH;N-α-t.-Boc-N-im-tosyl-L-histidine
- CAS NO.:35899-43-5
- Empirical Formula: C18H23N3O6S
- Molecular Weight: 409.46
- MDL number: MFCD00065967
- SAFETY DATA SHEET (SDS)
- Update Date: 2023-04-23 13:52:06
What is Boc-L-Histidine(Tosyl)?
Chemical properties
White to light yellow crystal powde
The Uses of Boc-L-Histidine(Tosyl)
Boc-L-His(Tos)-OH, is an amino acid building block used in peptide synthesis. With a growing peptide drug market the fast, reliable synthesis of peptides is of great importance.
Properties of Boc-L-Histidine(Tosyl)
Melting point: | ~125 °C (dec.) |
Density | 1.19 |
storage temp. | -20°C |
solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. |
form | powder to crystal |
pka | 3.50±0.10(Predicted) |
color | White to Almost white |
optical activity | [α]20/D +16±1°, c = 1% in methanol |
BRN | 769957 |
CAS DataBase Reference | 35899-43-5(CAS DataBase Reference) |
Safety information for Boc-L-Histidine(Tosyl)
Computed Descriptors for Boc-L-Histidine(Tosyl)
New Products
4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Mefenamic Acid IP/BP/EP/USP Diclofenac Sodium IP/BP/EP/USP Ornidazole IP Diclofenac Potassium SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
BOC-ORN(2-CL-Z)-OH
Chloral hydrate
1,1'-Carbonyldiimidazole
Vinylimidazole
Boc-L-Histidine(Tosyl)
1-BENZENESULFONYLIMIDAZOLE
1-[(4-Methylphenyl)sulfonyl]-1H-imidazole
BOC-HIS(MTS)-OH DCHA
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