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ChemicalBook--->CAS DataBase List--->756525-91-4

756525-91-4

756525-91-4 Structure

756525-91-4 Structure
IdentificationBack Directory
[Name]

BOC-15-AMINO-4,7,10,13-TETRAOXAPENTADECANOIC ACID
[CAS]

756525-91-4
[Synonyms]

Boc-NH-PEG4-COOH
Boc-N-amido-PEG4-acid
Boc-NH-PEG4-CH2CH2COOH
t-Boc-N-amido-PEG5-acid
t-Boc-N-amido-PEG4-acid
Carboxy-PEG4-(Boc-amine)
T-BOC-NH-AMIDO-PEG4-COOH
BOC-AMINO-PEG4-PROPANOIC ACID
(Boc-amino)-PEG4-carboxylic Acid
t-boc-N-amido-PEG4-propionic acid
Boc-NH-(PEG)-COOH (16 atoms) Novabiochem
BOC-15-AMINO-4,7,10,13-TETRAOXAPENTADECANOIC ACID
15-(Boc-aMino)-4,7,10,13-tetraoxapentadecanoic acid
2,2-DiMethyl-4-oxo-3,8,11,14,17-pentaoxa-5-azaicosan-20-oic acid
15-[(tert-Butoxycarbonyl)amino]-4,7,10,13-tetraoxapentadecanoic Acid
15-(Boc-amino)-4,7,10,13-tetraoxapentadecanoic acid purum, >=97.0% (TLC)
5,8,11,14-Tetraoxa-2-azaheptadecanedioic acid 1-(1,1-dimethylethyl) ester
N-(tert-Butyloxycarbonyl)-15-amino-4,7,10,13-tetraoxapentanedecanoic acid
3-[2-[2-[2-[2-(tert-Butoxycarbonylamino)ethoxy]ethoxy]ethoxy]ethoxy]propanoic acid
[Molecular Formula]

C16H31NO8
[MDL Number]

MFCD07781254
[MOL File]

756525-91-4.mol
[Molecular Weight]

365.42
Chemical PropertiesBack Directory
[Boiling point ]

504.5±50.0 °C(Predicted)
[density ]

1.124±0.06 g/cm3 (20 ºC 760 Torr)
[storage temp. ]

2-8°C
[form ]

Oil
[pka]

4.28±0.10(Predicted)
[color ]

Colorless to light yellow
[λmax]

254nm(lit.)
[InChI]

InChI=1S/C16H31NO8/c1-16(2,3)25-15(20)17-5-7-22-9-11-24-13-12-23-10-8-21-6-4-14(18)19/h4-13H2,1-3H3,(H,17,20)(H,18,19)
[InChIKey]

YCEYBRZRNOJORY-UHFFFAOYSA-N
[SMILES]

C(OC(C)(C)C)(=O)NCCOCCOCCOCCOCCC(O)=O
Safety DataBack Directory
[Safety Statements ]

24/25
[WGK Germany ]

3
[HS Code ]

29225090
Hazard InformationBack Directory
[Description]

t-Boc-N-amido-PEG4-acid is a PEG linker containing a terminal carboxylic acid and Boc-protected amino group. The hydrophilic PEG spacer increases solubility in aqueous media. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
[Chemical Properties]

Yellow oil
[Uses]

15-(Boc-amino)-4,7,10,13-tetraoxapentadecanoic acid is used as a substitution variant of cocaine esterase with improved stability and its use in treatment of cocaine overdose.
[Reactivity Profile]

reagent type: cross-linking reagent, reaction type: Pegylations
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