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ChemicalBook--->CAS DataBase List--->10436-25-6

10436-25-6

10436-25-6 Structure

10436-25-6 Structure
IdentificationMore
[Name]

BOC-11-AMINOUNDECANOIC ACID
[CAS]

10436-25-6
[Synonyms]

BOC-11-AUN-OH
BOC-NH-(CH2)10-COOH
Boc-11-aminoundecanoicaci
BOC-11-AMINOUNDECYLIC ACID
BOC-11-AMINOUNDECANOIC ACID
Boc-11-Aun-OH >=98.0% (TLC)
11-(BOC-AMINO)-UNDECANOIC ACID
N-ALPHA-T-BOC-11-AMINOUNDECANOIC ACID
REF DUPL: Boc-11-Aminoundecanoic acid
T-BUTOXYCARBONYL-11-AMINOUNDECYLIC ACID
10436-25-6 BOC-11-AMINOUNDECANOIC ACID
T-BUTOXYCARBONYL-11-AMINOUNDECANOIC ACID
N-T-BUTYLOXYCARBONYL-11-AMINO-UNDECANOIC ACID
N-(tert-Butoxycarbonyl)-11-aminoundecanoic acid
N-TERT-BUTYLOXYCARBONYL-11-AMINO-UNDECANOIC ACID
Boc-11-AMinoundecanoic acid Boc-11-AMinoundecanoic acid
11-[(2-methylpropan-2-yl)oxycarbonylamino]undecanoic acid
Undecanoic acid, 11-[[(1,1-dimethylethoxy)carbonyl]amino]-
[Molecular Formula]

C16H31NO4
[MDL Number]

MFCD00076902
[Molecular Weight]

301.42
[MOL File]

10436-25-6.mol
Chemical PropertiesBack Directory
[Melting point ]

67-68 °C
[Boiling point ]

441.9±18.0 °C(Predicted)
[density ]

1.006±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[pka]

4.78±0.10(Predicted)
[color ]

White to Almost white
[BRN ]

1975656
[CAS DataBase Reference]

10436-25-6(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[HS Code ]

2924.19.8000
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Description]

Boc-11-aminoundecanoic acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
[Chemical Properties]

White powder
[reaction suitability]

reaction type: Boc solid-phase peptide synthesis
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

10436-25-6(sigmaaldrich)
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