| Identification | More | [Name]
Cbz-D-Phenylalaninol | [CAS]
58917-85-4 | [Synonyms]
CBZ-D-PHENYLALANINOL
N-A-CBZ-D-PHENYLALANINOL
N-CARBOBENZOXY-D-PHENYLALANINOL
N-(CARBOBENZYLOXY)-D-PHENYLALANINOL
N-CBZ-D-PHENYLALANINOL
(R)-(+)-2-(BENZYLOXYCARBONYLAMINO)-3-PHENYL-1-PROPANOL
(R)-(+)-2-(CARBOBENZYLOXYAMINO)-3-PHENYL-1-PROPANOL
(R)-2-(Z-AMINO)-3-PHENYL-1-PROPANOL
(R)-BENZYLOXYCARBONYL-2-AMINO-3-PHENYL-1-PROPANOL
(R)-(+)-CARBOBENZYLOXYAMINO-3-PHENYL-1-PROPANOL
(R)-N-CARBOBENZOXY-2-AMINO-3-PHENYL-1-PROPANOL
(R)-N-CBZ-2-AMINO-3-PHENYL-1-PROPANOL
(R)-Z-PHENYLALANINOL
Z-D-PHENYLALANINOL
Z-D-PHE-OL
N-Benzyloxycarbonyl-D-phenylalaninol
N-alpha-Benzyloxycarbonyl-D-phenylalaninol
N-Benzyloxycarbonyl-D-phenylanlaninol, 98%
(R)-(+)-2-(Carbobenzyloxyamino)-3-phenyl-1-propanol, (R)-2-(Z-Amino)-3-phenyl-1-propanol, N-(Carbobenzyloxy)-D-phenylalaninol | [EINECS(EC#)]
1533716-785-6 | [Molecular Formula]
C17H19NO3 | [MDL Number]
MFCD00191193 | [Molecular Weight]
285.34 | [MOL File]
58917-85-4.mol |
| Chemical Properties | Back Directory | [Appearance]
white to light yellow crystal powde | [Melting point ]
92-95 °C | [alpha ]
30 º (c=1 in chloroform) | [Boiling point ]
427.77°C (rough estimate) | [density ]
1.0864 (rough estimate) | [refractive index ]
42 ° (C=2, MeOH) | [storage temp. ]
Store at 0-5°C | [pka]
11.86±0.46(Predicted) | [optical activity]
[α]22/D +30°, c = 1 in chloroform | [BRN ]
2221968 | [CAS DataBase Reference]
58917-85-4(CAS DataBase Reference) |
| Safety Data | Back 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 .
S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [F ]
10-23 | [HS Code ]
29051990 |
| Hazard Information | Back Directory | [Chemical Properties]
white to light yellow crystal powde | [Uses]
Z-D-Phenylalaninol is used in the synthesis of aminophenylpropanyl phosphate derivatives which has pin1 inhibitory activity. |
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