| Identification | Back Directory | [Name]
1,5-bis-Boc-1,5,10-triazadecane | [CAS]
85503-20-4 | [Synonyms]
N1,N4-Bis-spermidine
N1,N4-bis-Boc-sperMidine
1,5-bis-Boc-1,5,10-triazadecane
N1,N4-Bis-Boc-spermidine >=95.0% (TLC)
tert-butyl (4-aminobutyl)(3-((tert-butoxycarbonyl)amino)propyl)carbamate
tert-butyl N-(4-aminobutyl)-N-[3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]carbamate
N-(4-aminobutyl)-N-[3-[[(1,1-dimethylethoxy)carbonyl]amino]propyl]Carbamic acid 1,1-dimethylethyl ester
Carbamic acid, N-(4-aminobutyl)-N-[3-[[(1,1-dimethylethoxy)carbonyl]amino]propyl]-, 1,1-dimethylethyl ester | [Molecular Formula]
C17H35N3O4 | [MDL Number]
MFCD16875671 | [MOL File]
85503-20-4.mol | [Molecular Weight]
345.48 |
| Chemical Properties | Back Directory | [storage temp. ]
-20°C | [form ]
liquid | [BRN ]
6418809 | [InChI]
1S/C17H35N3O4/c1-16(2,3)23-14(21)19-11-9-13-20(12-8-7-10-18)15(22)24-17(4,5)6/h7-13,18H2,1-6H3,(H,19,21) | [InChIKey]
GQZZMJDEWJRWRP-UHFFFAOYSA-N | [SMILES]
CC(C)(C)OC(=O)NCCCN(CCCCN)C(=O)OC(C)(C)C |
| Hazard Information | Back Directory | [Description]
1,5-Bis-Boc-1,5,10-triazadecane is a linker containing an amino group with two Boc-protected amino groups. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc group can be deprotected under mild acidic conditions to form the free amine. | [Uses]
N1,N4-Bis-Boc-spermidine is an antibiotic enhancers against resistant gram-negative bacteria and it is an anticancer agent. | [reaction suitability]
reagent type: cross-linking reagent |
|
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Sigma-Aldrich
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