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ChemicalBook--->CAS DataBase List--->51219-19-3

51219-19-3

51219-19-3 Structure

51219-19-3 Structure
IdentificationBack Directory
[Name]

BOC-ARG(Z)2-OH
[CAS]

51219-19-3
[Synonyms]

BOC-ARG(Z)2-OH
BOC-L-ARG(Z2)-OH
BOC-ARG(DI-Z)-OH
BOC-ARGININE(Z)2-OH
Boc-Arg(Z)2-OH >=98.0% (TLC)
Boc-Arg(di-Z)-OH Novabiochem
Nα-Boc-Nω,Nω'-bis-Z-L-arginine
(Tert-Butoxy)Carbonyl Arg(Z)2-OH
BOC-L-DIBENZYLOXYCARBONYL ARGININE
N-ALPHA-BOC-NG,NG-BIS-CBZ-L-ARGININE
BOC-N-OMEGA,N-OMEGA'-BIS-Z-L-ARGININE
Nα-Boc-Nω,Nω'-bis-Z-L-arginine≥ 98% (HPLC)
N-ALPHA-BOC-N-DELTA,N-OMEGA-DI-Z-L-ARGININE
N-.ALPHA.-BOC-N-.OMEGA.-,N-.OMEGA.''-DI-CBZ-L-ARGININE
N,N-Bis-(benzyloxycarbonyl)-N-tert-butoxycarbonyl-L-arginine
N-ALPHA-T-BUTOXYCARBONYL-N-OMEGA1,N-OMEGA2-BIS-CARBOBENZOXY-L-ARGININE
(S)-5-(1,3-Bis((benzyloxy)carbonyl)guanidino)-2-((tert-butoxycarbonyl)amino)pentanoic acid
(2S)-5-{[(benzyloxy)carbonyl]({[(benzyloxy)carbonyl]amino}methanimidoyl)amino}-2-{[(tert-butoxy)carbonyl]amino}pentanoic acid
11-Oxa-2,4,9-triazatridecanoic acid, 8-carboxy-3-imino-12,12-dimethyl-10-oxo-4-[(phenylmethoxy)carbonyl]-, 1,3-bis(phenylmethyl) ester, (8S)-
[Molecular Formula]

C27H34N4O8
[MDL Number]

MFCD00236824
[MOL File]

51219-19-3.mol
[Molecular Weight]

542.58
Chemical PropertiesBack Directory
[Melting point ]

~140 °C (dec.)
[density ]

1.24±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform (Sparingly), DMSO (Slightly), Methanol (Slightly, Heated)
[form ]

Solid
[pka]

3.96±0.21(Predicted)
[color ]

White to Off-White
[optical activity]

[α]20/D +2.5±0.5°, c = 1% in methanol
[BRN ]

4914609
Safety DataBack Directory
[Safety Statements ]

22-24/25
[WGK Germany ]

3
[HS Code ]

2925 29 00
Hazard InformationBack Directory
[Chemical Properties]

White to off-white powder
[Uses]

Boc-Arg(Z)2-OH is used as a reagent in the preparation of antimalarial, antileishmanial, antimicrobial, cytotoxicity, and metHb formation activities of amino acid amides of quinolinamines
[reaction suitability]

reaction type: Boc solid-phase peptide synthesis
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