| Identification | More | [Name]
BOC-HIS(DNP)-OH | [CAS]
25024-53-7 | [Synonyms]
BOC-HIS(DNP)-OH BOC-L-DINITROPHENYL HISTIDINE BOC-L-HIS(DNP)-OH BOC-L-HISTIDINE (DNP) N-ALPHA-BOC-NIM-2,4-DINITROPHENYL-L-HISTIDINE N-ALPHA-BOC-NIM-DINITROPHENYL-L-HISTIDINE N-ALPHA-T-BOC-N-IM-2,4-DINITROPHENYL-L-HISTIDINE N-ALPHA-T-BOC-N-IM-DINITROPHENYL-L-HISTIDINE TBOC-L-HISTIDINE (DNP) n-[(1,1-dimethylethoxy)carbonyl]-1-(2,4-dinitrophenyl)-l-histidin Nα-Boc-N(im)-2,4-dinitrophenyl-L-histidine
na-T-boc-N-im-dnp-L-histidine N-(tert-butoxycarbonyl)-1-(2,4-dinitrophenyl)-L-histidine N-α-Boc-N-im-dinitrophenyl-L-histidine nα-boc-n(im)-2,4-dinitrophenyl-l-histidine NA-BOC-N(IM)-2,4-DINITROPHENYL-L-HISTIDINE N2-BOC-N-IM-DINITROPHENYL-L-HISTIDINE Nalpha-(tert-butoxycarbonyl)-N-dinitrophenyl-L-histidine Nα-[(1,1-Dimethylethoxy)carbonyl]-1-(2,4-dinitrophenyl)-L-histidine | [EINECS(EC#)]
246-569-0 | [Molecular Formula]
C17H19N5O8 | [MDL Number]
MFCD00065966 | [Molecular Weight]
421.36 | [MOL File]
25024-53-7.mol |
| Questions And Answer | Back Directory | [Synthesis]
Starting with 2,4-dinitrophenyl-L-histidine, the target compound BOC-HIS(DNP)-OH was prepared by an amino-protection reaction with di-tert-butyl dicarbonate. 
Figure 1 Synthesis of BOC-HIS(DNP)-OH Experimental Procedure: 2,4-Dinitrophenyl-L-histidine was dissolved in 100 mL of sodium hydroxide aqueous solution. 200 mL of tetrahydrofuran and 250 g of di-tert-butyl dicarbonate were added sequentially. The pH was controlled at 8-9. After reacting for 12 h, the mixture was extracted twice with 500 mL of ethyl acetate each time. The aqueous phase was then acidified with HCl to pH 1-2, and the product was extracted three times with 500 mL of ethyl acetate each time. The ester layers were combined and washed twice with 200 mL of saturated brine each time. The mixture was dried over anhydrous sodium sulfate for 12 h, filtered, concentrated, crystallized, and dried at 40-50 °C to obtain BOC-HIS(DNP)-OH. |
| Safety Data | Back Directory | [Safety Statements ]
S22:Do not breathe dust . S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [F ]
8 | [TSCA ]
Yes |
| Hazard Information | Back Directory | [Chemical Properties]
Yellow solid | [Uses]
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff. | [Uses]
The Dnp group is stable to HF and TFMSA. | [reaction suitability]
reaction type: Boc solid-phase peptide synthesis |
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J & K SCIENTIFIC LTD.
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Alfa Aesar
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http://chemicals.thermofisher.cn |
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Energy Chemical
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