| Identification | More | [Name]
Boc-L-Histidine(Tosyl) | [CAS]
35899-43-5 | [Synonyms]
BOC-HISTIDINE(TOS)-OH
BOC-HIS(TOS)
BOC-HIS(TOS)-OH
BOC-HIS(TOS)-OH IPA
BOC-L-HISTIDINE(TOSYL)
BOC-L-HIS(TOS)
BOC-L-HIS(TOS)-OH
BOC-N-IM-4-TOLUENESYLFONYL-L-HISTIDINE
N-ALPHA-BOC-N(IM)-TOSYL-L-HISTIDINE
N-ALPHA-BOC-NIM-TOSYL-L-HISTIDINE ISOPROPYL ALCOHOL
NALPHA-BOC-TELE-TOSYL-L-HISTIDINE
N-ALPHA-T-BOC-IM-TOSYL-L-HIS
N-ALPHA-T-BOC-N-IM-TOSYL-L-HISTIDINE
N ALPHA-T-BUTOXYCARBONYL-N(IM)-TOSYL-L-HISTIDINE
N-ALPHA-T-BUTOXYCARBONYL-N-TAU-TOSYL-L-HISTIDINE
N-ALPHA-T-BUTYLOXYCARBONYL-N-TAU-TOSYL-L-HISTIDINE
NALPHA-TERT-BUTOXYCARBONYL-N(IM)-TOSYL-L-HISTIDINE
N-(ALPHA)-(TERT-BUTOXYCARBONYL)-TAU-(P-TOLUENESULFONYL)-L-HISTIDINE
NALPHA-(TERT-BUTOXYCARBONYL)-TELE-(P-TOLUENESULFONYL)-L-HISTIDINE
NALPHA-(TERT-BUTOXYCARBONYL)-T-(P-TOLUENESULFONYL)-L-HISTIDINE | [Molecular Formula]
C18H23N3O6S | [MDL Number]
MFCD00065967 | [Molecular Weight]
409.46 | [MOL File]
35899-43-5.mol |
| Chemical Properties | Back Directory | [Appearance]
White to light yellow crystal powde | [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 Rotation]
[α]20/D +16±1°, c = 1% in methanol | [BRN ]
769957 | [Major Application]
peptide synthesis | [InChI]
1S/C18H23N3O6S/c1-12-5-7-14(8-6-12)28(25,26)21-10-13(19-11-21)9-15(16(22)23)20-17(24)27-18(2,3)4/h5-8,10-11,15H,9H2,1-4H3,(H,20,24)(H,22,23)/t15-/m0/s1 | [InChIKey]
DCLJSEPKYJSEHW-HNNXBMFYSA-N | [SMILES]
Cc1ccc(cc1)S(=O)(=O)n2cnc(C[C@H](NC(=O)OC(C)(C)C)C(O)=O)c2 | [CAS DataBase Reference]
35899-43-5(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Chemical Properties]
White to light yellow crystal powde | [Uses]
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. | [reaction suitability]
reaction type: Boc solid-phase peptide synthesis |
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