ChemicalBook--->CAS DataBase List--->50913-12-7

50913-12-7

50913-12-7 Structure

50913-12-7 Structure
IdentificationBack Directory
[Name]

BOC-D-ARG(NO2)-OH
[CAS]

50913-12-7
[Synonyms]

Boc-D-Arg(NO)-OH
BOC-D-ARG(NO2)-OH
BOC-D-NITROARGININE
Agatraban impurity 1
BOC-D-ARGININE(NITRO)
BOC-D-ARGININE(NO2)-OH
Boc-Nw-nitro-D-arginine
N'-Nitro-N-Boc-D-arginine
Na-Boc-N-nitro-D-arginine
Nα-Boc-Nω-nitro-D-arginine
Na-Boc-Nw-nitro-D-arginine
OMEGA-NITRO-BOC-D-ARGININE
BOC-N-OMEGA-NITRO-D-ARGININE
N-α-Boc-N-ω-nitro-D-arginine
N-ALPHA-T-BOC-NG-NITRO-D-ARGININE
(Tert-Butoxy)Carbonyl D-Arg(NO2)-OH
Nα-Boc-Nω-nitro-D-arginine USP/EP/BP
Nα-Boc-Nω-nitro-D-arginine≥ 99% (HPLC)
N-.ALPHA.-BOC-N-.OMEGA.-NITRO-D-ARGININE
N-ALPHA-T-BUTOXYCARBONYL-N-G-NITRO-D-ARGININE
Boc-D-Arg(NO2)-OH N-α-Boc-N-ω-nitro-D-arginine
N-alpha-tert-Butoxycarbonyl-N-omega-nitro-D-arginine
N2-[(1,1-DiMethylethoxy)carbonyl]-N5-[iMino(nitroaMino)Methyl]-D-ornithine
D-Ornithine, N2-[(1,1-dimethylethoxy)carbonyl]-N5-[imino(nitroamino)methyl]-
(2R)-2-{[(tert-butoxy)carbonyl]amino}-5-(N'-nitrocarbamimidamido)pentanoic acid
(2R)-2-(tert-butoxycarbonylamino)-5-[(N-nitrocarbamimidoyl)amino]pentanoic acid
N2-[(1,1-Dimethylethoxy)carbonyl]-N5-[imino(nitroamino)methyl]-D-ornithine (Afatinib Impurity)
(2R)-5-[[amino(nitramido)methylidene]amino]-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoicaci
(2R)-5-[[amino(nitramido)methylidene]amino]-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic acid
(2R)-5-[[amino(nitramido)methylidene]amino]-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]pentanoic acid
[Molecular Formula]

C11H21N5O6
[MDL Number]

MFCD00038091
[MOL File]

50913-12-7.mol
[Molecular Weight]

319.31
Chemical PropertiesBack Directory
[density ]

1.40±0.1 g/cm3(Predicted)
[storage temp. ]

-15°C
[pka]

3.84±0.50(Predicted)
Safety DataBack Directory
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Chemical Properties]

White Solid
[Uses]

Nα-Boc-Nω-nitro-D-arginine is used in the synthesis of selective inactivators of human plasma kallikrein via chloromethyl ketone formation. Nα-Boc-Nω-nitro-D-arginine also produced modest inhibition of the effects acetylcholine in rabbit aorta.
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