| Identification | More | [Name]
N-Boc-cadaverine | [CAS]
51644-96-3 | [Synonyms]
1-BOC-AMINO-1,5-PENTANEDIAMINE
BOC-1,5-DIAMINOPENTANE
BOC-1,5-DIAMINOPENTANE HCL
BOC-1,5-DIAMINOPENTANE HYDROCHLORIDE
BOC-DAPE HCL
BOC-DAPE-OH
BOC-DIAMINOPENTANE HCL
BOC-NH(CH2)5NH2 HCL
N-1-BOC-1,5-DIAMINOPENTANE HCL
N-1-T-BUTOXYCARBONYL-1,5-DIAMINOPENTANE HYDROCHLORIDE
N-(5-AMINOAMYL)CARBAMIC ACID TERT-BUTYL ESTER
N-(5-AMINOPENTYL)CARBAMIC ACID TERT-BUTYL ESTER
N-BOC-1,5-DIAMINOPENTANE
N-BOC-1,5-PENTANEDIAMINE
N-Boc-cadaverine
N-T-BUTYLOXYCARBONYL-1,5-DIAMINOPENTANE HYDROCHLORIDE
N-(TERT-BUTOXYCARBONYL)-1,5-DIAMINOPENTANE
N-(TERT-BUTOXYCARBONYL)-1,5-PENTANEDIAMINE
N-TERT-BUTYLOXYCARBONYL-1,5-DIAMINOPENTANE HYDROCHLORIDE
TERT-BUTYL N-(5-AMINOAMYL)CARBAMATE | [Molecular Formula]
C10H22N2O2 | [MDL Number]
MFCD00210020 | [Molecular Weight]
202.29 | [MOL File]
51644-96-3.mol |
| Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R34:Causes burns. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
UN 2735 8/PG 3
| [WGK Germany ]
3
| [F ]
10-34 | [HazardClass ]
8 | [PackingGroup ]
Ⅲ | [HS Code ]
2924190090 |
| Hazard Information | Back Directory | [Description]
tert-Butyl (5-aminopentyl)carbamate can be used as a PROTAC linker in the synthesis of PROTACs. tert-Butyl (5-aminopentyl)carbamate is an alkane chain with terminal amine and Boc-protected amino groups. Amine 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]
Some of the reported applications of N-Boc-cadaverine include:
- Synthesis of of a supermacrocycle that self-assemble to form organic nanotubes.
- Preparation of water-soluble unsymmetrical sulforhodamine fluorophores from monobrominated sulfoxanthene dye.
- Synthesis of functionalized porphyrins as biocompatible carrier system for photodynamic therapy (PDT).
|
|
|