| Identification | More | [Name]
Boc-beta-alanine | [CAS]
3303-84-2 | [Synonyms]
3-TERT-BUTOXYCARBONYLAMINOPROPIONIC ACID
BOC-B-ALA-OH
BOC-BETA-ALA
BOC-BETA-ALANINE
BOC-BETA-ALA-OH
BOC-GLY(C*CH2)-OH
BOC-NH-(CH2)2-COOH
N-ALPHA-TERT-BUTYLOXYCARBONYL-BETA-ALANINE
N-BETA-T-BOC-BETA-ALANINE
N-BETA-T-BUTOXYCARBONYL-BETA-ALANINE
N-BETA-T-BUTOXYCARBONYL-BETA-AMINOPROPIONIC ACID
N-BOC-BETA-ALANINE
N-T-BOC-BETA-ALANINE
N-T-BUTOXYCARBONYL-BETA-ALANINE
N-TERT-BOC-BETA-ALANINE
N-TERT-BUTOXYCARBONYL-BETA-ALANINE
RARECHEM EM WB 0003
T-BUTYLOXYCARBONYL-BETA-ALANINE
Boc-ß
-Ala-OH
Butoxycarbonylalanine | [EINECS(EC#)]
221-979-2 | [Molecular Formula]
C8H15NO4 | [MDL Number]
MFCD00037291 | [Molecular Weight]
189.21 | [MOL File]
3303-84-2.mol |
| Chemical Properties | Back Directory | [Melting point ]
76-78 °C
| [Boiling point ]
333.9±25.0 °C(Predicted) | [density ]
1.129±0.06 g/cm3(Predicted) | [storage temp. ]
Store at 0°C | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
Crystalline Powder | [pka]
4.46±0.10(Predicted) | [color ]
White to off-white | [BRN ]
1909986 | [InChIKey]
WCFJUSRQHZPVKY-UHFFFAOYSA-N | [CAS DataBase Reference]
3303-84-2(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
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 .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [HazardClass ]
IRRITANT | [HS Code ]
29241990 |
| Hazard Information | Back Directory | [Description]
Boc-beta-Ala-OH 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 solid | [Uses]
Boc-?β-?Ala-?OH is a reagent used in the synthesis of quinazolines as platelet aggregation inhibitors and ligands of integrin. | [reaction suitability]
reaction type: Boc solid-phase peptide synthesis |
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