25024-53-7Relevant articles and documents
Use of N-im-dinitrophenylhistidine in the solid-phase synthesis of the tricosapeptides 124-146 of human hemoglobin beta chain.
Chillemi,Merrifield
, p. 4344 - 4346 (1969)
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Alfa Aesar
(H63421) N-Boc-1-(2,4-dinitrophenyl)-L-histidine, 99%
25024-53-7
5g
459.0CNY
Alfa Aesar
(H63421) N-Boc-1-(2,4-dinitrophenyl)-L-histidine, 99%
25024-53-7
25g
1833.0CNY
Alfa Aesar
(H63421) N-Boc-1-(2,4-dinitrophenyl)-L-histidine, 99%
25024-53-7
100g
7340.0CNY
Aldrich
(15287) Boc-His(Dnp)-OH ≥98.0% (TLC)
25024-53-7
15287-5G
556.92CNY
Version: 1.0
Creation Date: Aug 12, 2017
Revision Date: Aug 12, 2017
Product name | (2S)-3-[1-(2,4-dinitrophenyl)imidazol-4-yl]-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid |
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Product number | - |
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Other names | Boc-L-His(Dnp)-OH |
Identified uses | For industry use only. |
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Uses advised against | no data available |
Emergency phone number | - |
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Service hours | Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours). |
More Details:25024-53-7 SDS
(4R)-thiazolidine-4-carboxamide
Boc-His(Dnp)-OH
Boc-His(DNP)-Tzl-NH2
Conditions | Yield |
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With benzotriazol-1-ol; dicyclohexyl-carbodiimide In dichloromethane at 25℃; for 4h; | 96% |
3-hydroxy-1,2,3-benzotriazin-4(3H)-one ethylammonium salt
Boc-His(Dnp)-OH
Boc-His(τ-Dnp)-NH-Et
Conditions | Yield |
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With dicyclohexyl-carbodiimide In N,N-dimethyl-formamide 1) 0 deg C, 1 h, 2) RT, 2 h; | 93% |
Boc-His(Dnp)-OH
Boc-His(τ-Dnp)-NH2
Conditions | Yield |
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With 3-hydroxy-1,2,3-benzotriazin-4(3H)-one ammonium salt; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide 1) 0 deg C, 1 h, 2) RT, 2 h; | 93% |
Boc-His(Dnp)-OH
Nα-tert-butoxycarbonyl-Nim-2,4-dinitrophenyl-L-histidyl-L-leucyl-O-benzyl-L-tyrosine benzyl ester
Conditions | Yield |
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With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; isopropylamine; isopropyl alcohol In N,N-dimethyl-formamide Ambient temperature; | 90% |
3-hydroxy-1,2,3-benzotriazin-4(3H)-one methylammonium salt
Boc-His(Dnp)-OH
Boc-His(τ-Dnp)-NH-Me
Conditions | Yield |
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With dicyclohexyl-carbodiimide In N,N-dimethyl-formamide 1) 0 deg C, 1 h, 2) RT, 2 h; | 89% |
Conditions | Yield |
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Stage #1: Boc-His(Dnp)-OH With benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine In dichloromethane for 0.5h; Cooling with ice; Stage #2: glycine ethyl ester hydrochloride With triethylamine In dichloromethane at 20℃; Cooling with ice; | 85.4% |
(2S,3S)-2-Amino-1-cyclohexyl-5-(pyridin-2-ylsulfanyl)-pentan-3-ol; hydrochloride
Boc-His(Dnp)-OH
{(S)-1-[(1S,2S)-1-Cyclohexylmethyl-2-hydroxy-4-(pyridin-2-ylsulfanyl)-butylcarbamoyl]-2-[1-(2,4-dinitro-phenyl)-1H-imidazol-4-yl]-ethyl}-carbamic acid tert-butyl ester
Conditions | Yield |
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With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide for 14h; Ambient temperature; | 79% |
4-Aminobutanol
Boc-His(Dnp)-OH
4-[Nα-tert-butyloxycarbonyl-NIm(1)-(2,4-dinitrophenyl)-L-histidyl]aminobutan-1-ol
Conditions | Yield |
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With 2,3,4,5,6-pentafluorophenol; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 0.666667h; Substitution; | 78% |
2,4,5-trichlorophenol
Boc-His(Dnp)-OH
Nα-(tert-butyloxycarbonyl)-Nim-(2,4-dinitrophenyl)-L-histidine 2,4,5-trichlorophenyl ester
Conditions | Yield |
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With dicyclohexyl-carbodiimide In ethyl acetate at -5℃; | 77% |
(2S,3R,4S)-2-amino-1-cyclohexyl-3,4-dihydroxy-6-(2-pyridyl)hexane
Boc-His(Dnp)-OH
N-im-(2,4-dinitrophenyl)-L-histidyl>-(2S,3R,4S)-1-cyclohexyl-3,4-dihydroxy-6-(2-pyridyl)hexan-2-amine
Conditions | Yield |
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With N-ethylmorpholine;; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate In N,N-dimethyl-formamide for 24h; Ambient temperature; | 65.3% |
dopamine hydrochloride
Boc-His(Dnp)-OH
N-[Nα-tert-butoxycarbonyl-Nτ-(2,4-dinitrophenyl)-L-histidinyl]dopamine
Conditions | Yield |
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With acetic acid In methanol; dichloromethane; ethyl acetate | 56% |
-(2-amino-3-cyclohexyl-1-hydroxypropyl)phosphonic acid, dimethyl ester, hydrochloride
Boc-His(Dnp)-OH
((1S,2S)-2-{(S)-2-tert-Butoxycarbonylamino-3-[1-(2,4-dinitro-phenyl)-1H-imidazol-4-yl]-propionylamino}-3-cyclohexyl-1-hydroxy-propyl)-phosphonic acid dimethyl ester
Conditions | Yield |
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With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In N,N-dimethyl-formamide | 55% |
3,4-dihydroxybenzylamine hydrobromide
Boc-His(Dnp)-OH
N-[Nα-tert-Butoxycarbonyl-Nτ-(2,4-dinitrophenyl)-L-histidinyl]-3,4-dihydroxybenzylamine
Conditions | Yield |
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With acetic acid In methanol; dichloromethane; ethyl acetate | 40% |
2-(4-(triphenylmethylthio)phenyl)acetic acid
1-(tert-butoxycarbonyl)-L-proline
t-Boc-L-valine
N-(tert-butyloxycarbonyl)-L-isoleucine
N-tert-butoxycarbonyl-L-leucine
L-N-Boc-Ala
N-tert-butoxycarbonyl-L-methionine
BOC-L-aspartic acid 4-benzyl ester
N-Boc-O-benzyl-L-threonine
Boc-Glu
Boc-(S)-Lys(2-Cl-Z)-OH
(S)-3-[4-(2-Bromo-benzyloxycarbonyloxy)-phenyl]-2-tert-butoxycarbonylamino-propionic acid
Nα-t-butoxycarbonyl-Nδ-xanthydryl-L-glutamine
Boc-His(Dnp)-OH
Conditions | Yield |
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Stage #1: 2-(4-(triphenylmethylthio)phenyl)acetic acid With dmap; diisopropyl-carbodiimide In dichloromethane at 20℃; for 1h; Stage #2: With triethylsilane; trifluoroacetic acid In dichloromethane; water Stage #3: 1-(tert-butoxycarbonyl)-L-proline; t-Boc-L-valine; N-(tert-butyloxycarbonyl)-L-isoleucine; N-tert-butoxycarbonyl-L-leucine; L-N-Boc-Ala; N-tert-butoxycarbonyl-L-methionine; BOC-L-aspartic acid 4-benzyl ester; N-Boc-O-benzyl-L-threonine; Boc-Glu; Boc-(S)-Lys(2-Cl-Z)-OH; (S)-3-[4-(2-Bromo-benzyloxycarbonyloxy)-phenyl]-2-tert-butoxycarbonylamino-propionic acid; Nα-t-butoxycarbonyl-Nδ-xanthydryl-L-glutamine; Boc-His(Dnp)-OH Further stages; | 14% |
BOC-glycine
t-Boc-L-valine
N-(tert-butyloxycarbonyl)-L-isoleucine
N-tert-butoxycarbonyl-L-leucine
L-N-Boc-Ala
N-tert-butoxycarbonyl-L-phenylalanine
N-Boc-O-benzyl-L-threonine
Boc-Arg(Tos)-OH
BOC-O-benzyl-L-serine
Boc-Asp(O-cyclohexyl)-OH
N-α-tert-butyloxycarbonyl-glutamic acid, γ-cyclohexyl ester
(S)-3-[4-(2-Bromo-benzyloxycarbonyloxy)-phenyl]-2-tert-butoxycarbonylamino-propionic acid
S-<(4-methylphenyl)methyl>-L-cysteine
Nα-tert-butoxycarbonyl-1-formyl-L-tryptophan
(S)-2-tert-Butoxycarbonylamino-N-(9H-xanthen-9-yl)-succinamic acid
Boc-His(Dnp)-OH
Boc-Lys(Pg)-OH
Boc-Gln(Pg)-OH
CSQFNDTLNVYLTAHNALGSSLHTAGVDLAKSLRIAAKIYSEADEAWRKAIDGLFT
Conditions | Yield |
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Stage #1: Boc-Thr(benzyl)-PAM dicyclohexylammonium salt With diisopropyl-carbodiimide In dichloromethane for 1h; Stage #2: With trifluoroacetic acid In dichloromethane for 0.0333333h; Stage #3: BOC-glycine; t-Boc-L-valine; N-(tert-butyloxycarbonyl)-L-isoleucine; N-tert-butoxycarbonyl-L-leucine; L-N-Boc-Ala; N-tert-butoxycarbonyl-L-phenylalanine; N-Boc-O-benzyl-L-threonine; Boc-Arg(Tos)-OH; BOC-O-benzyl-L-serine; Boc-Asp(O-cyclohexyl)-OH; N-α-tert-butyloxycarbonyl-glutamic acid, γ-cyclohexyl ester; (S)-3-[4-(2-Bromo-benzyloxycarbonyloxy)-phenyl]-2-tert-butoxycarbonylamino-propionic acid; S-<(4-methylphenyl)methyl>-L-cysteine; Nα-tert-butoxycarbonyl-1-formyl-L-tryptophan; (S)-2-tert-Butoxycarbonylamino-N-(9H-xanthen-9-yl)-succinamic acid; Boc-His(Dnp)-OH; Boc-Lys(Pg)-OH; Boc-Gln(Pg)-OH Further stages; | 10.2% |
1-(tert-butoxycarbonyl)-L-proline
t-Boc-L-valine
N-tert-butoxycarbonyl-L-leucine
L-N-Boc-Ala
Boc-Gln-OH
N-(fluoren-9-ylmethoxycarbonyl)glycine
N-tert-butoxycarbonyl-L-phenylalanine
Boc-Arg(Tos)-OH
BOC-O-benzyl-L-serine
O-benzyl-N-Fmoc-L-serine
N-α-tert-butyloxycarbonyl-glutamic acid, γ-cyclohexyl ester
Boc-(S)-Lys(2-Cl-Z)-OH
Boc-His(Dnp)-OH
Conditions | Yield |
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Stage #1: Boc-Arg(Tos)-OH With benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate In N,N-dimethyl-formamide for 2h; Stage #2: With piperidine In 1-methyl-pyrrolidin-2-one for 0.5h; Stage #3: 1-(tert-butoxycarbonyl)-L-proline; t-Boc-L-valine; N-tert-butoxycarbonyl-L-leucine; L-N-Boc-Ala; Boc-Gln-OH; N-(fluoren-9-ylmethoxycarbonyl)glycine; N-tert-butoxycarbonyl-L-phenylalanine; 2-(decyldisulfanyl)pyridine; BOC-O-benzyl-L-serine; O-benzyl-N-Fmoc-L-serine; N-α-tert-butyloxycarbonyl-glutamic acid, γ-cyclohexyl ester; Boc-(S)-Lys(2-Cl-Z)-OH; Boc-His(Dnp)-OH; fmoc-S-4-methoxytrityl-L-cysteine Further stages; | 10.2% |
Conditions | Yield |
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With dicyclohexyl-carbodiimide In tetrahydrofuran at 5℃; for 2.5h; | 5.06 g |
1-(tert-butoxycarbonyl)-L-proline
(2S)-6-oxopipecolic acid
Boc-His(Dnp)-OH
<*>Aad-His-Pro-NH2
Conditions | Yield |
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Yield given. Multistep reaction; |
BOC-O-benzyl-L-serine
Boc-Trp-OH
Boc-His(Dnp)-OH
L-Pyroglutamic acid
pGlu-His-Trp-Ser
Conditions | Yield |
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Yield given. Multistep reaction; |
4-nitro-phenol
Boc-His(Dnp)-OH
Nα-(tert-Butyloxycarbonyl)-N(im)-(2,4-dinitrophenyl)-L-histidine p-nitrophenyl ester
Conditions | Yield |
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With pyridine; dicyclohexyl-carbodiimide In tetrahydrofuran for 24h; Ambient temperature; |
isopropyl (3S,4S)-4-amino-5-cyclohexyl-3-hydroxypentanoate*HCl
Boc-His(Dnp)-OH
Conditions | Yield |
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With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide for 14h; Ambient temperature; |
2HCl*H-LeuΨ(CH2NH)Met-NH2
Boc-His(Dnp)-OH
Boc-His(Dnp)-LeuΨ(CH2NH)Met-NH2
Conditions | Yield |
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With 4-methyl-morpholine |
p-(bromoacetamido)azobenzene
Boc-His(Dnp)-OH
Conditions | Yield |
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With 15-crown-5; sodium methylate In methanol; N,N-dimethyl-formamide at 50℃; for 0.5h; |
Boc-His(Dnp)-OH
Conditions | Yield |
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With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide for 14h; Ambient temperature; |
Boc-His(Dnp)-OH
Conditions | Yield |
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With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide for 14h; Ambient temperature; |
Boc-His(Dnp)-OH
Conditions | Yield |
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With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide for 14h; Ambient temperature; |
Boc-His(Dnp)-OH
Conditions | Yield |
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With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide for 14h; Ambient temperature; |
Boc-His(Dnp)-OH
Conditions | Yield |
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With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide for 14h; Ambient temperature; |
Conditions | Yield |
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With 4-methyl-morpholine; isobutyl chloroformate 1) THF, -30 to -15 degC, 12 min; 2) THF, -30 degC, 1 h; room temp., overnight; Yield given. Multistep reaction; |
Conditions | Yield |
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With 4-methyl-morpholine In ethyl acetate at -23℃; for 0.5h; |
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