| Identification | More | [Name]
N-Boc-2-piperidinecarboxylic acid | [CAS]
98303-20-9 | [Synonyms]
(+/-)-1-BOC-PIPERIDINE-2-CARBOXYLIC ACID
1-N-BOC-2-PIPERIDINECARBOXYLIC ACID
1-(TERT-BUTOXYCARBONYL)PIPERIDINE-2-CARBOXYLIC ACID
BOC-DL-HOMOPROLINE
BOC-DL-HOMOPRO-OH
BOC-DL-HOPRO-OH
BOC-DL-PIC(2)-OH
BOC-DL-PIPECOLIC ACID
BOC-DL-PIP-OH
BOC-(RS)-PIPERIDINE-2-CARBOXYLIC ACID
N-ALPHA-T-BUTOXYCARBONYL-DL-HOMOPROLINE
N-ALPHA-T-BUTOXYCARBONYL-DL-PIPECOLIC ACID
N-BOC-2-PIPERIDINECARBOXYLIC ACID
N-BOC-DL-PIPECOLINIC ACID
N-BOC-PIPERIDINE-2-CARBOXYLIC ACID
N-TERT-BUTOXYCARBONYL-2-PIPERIDINECARBOXYLIC ACID
PIPERIDINE-1,2-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER
RAC 1-BOC-PIPERIDINE-2-CARBOXYLIC ACID
RAC 1-TERT-BUTOXYCARBONYL-PIPERIDINE-2-CARBOXYLIC ACID
RARECHEM AH CK 0059 | [EINECS(EC#)]
628-632-8 | [Molecular Formula]
C11H19NO4 | [MDL Number]
MFCD01862877 | [Molecular Weight]
229.27 | [MOL File]
98303-20-9.mol |
| Chemical Properties | Back Directory | [Appearance]
White crystalline powder | [Melting point ]
130-133 °C (lit.) | [Boiling point ]
353.2±35.0 °C(Predicted) | [density ]
1.164±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
Crystalline Powder | [pka]
4.03±0.20(Predicted) | [color ]
White | [Detection Methods]
Differential,NMR | [BRN ]
480022 | [InChIKey]
JQAOHGMPAAWWQO-UHFFFAOYSA-N | [CAS DataBase Reference]
98303-20-9(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [F ]
10 | [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
29339900 |
| Hazard Information | Back Directory | [Chemical Properties]
White crystalline powder | [Uses]
DL-Boc-pipecolic acid is the protected form of Pipecolic acid (P479760). Pipecolic acid is an intemediary metabolite of L-Lysine (L468895). Its accumulation in the body is characteristic of peroxisomal disorders in infants (such as Zeilweiger syndrome). Pipecolic acid is also used as a catalyst in asymmetric Mannich reactions. |
|
|