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79069-15-1

79069-15-1 Structure

79069-15-1 Structure
IdentificationMore
[Name]

N-Boc-(S)-2-amino-3-benzyloxy-1-propanol
[CAS]

79069-15-1
[Synonyms]

BOC-D-SER(BZL)-OL
BOC-D-SERINOL(BZL)
BOC-O-BENZYL-D-SERINOL
BOC-O-BENZYL-L-SERINOL
BOC-(R)-2-AMINO-3-PHENYLMETHOXY-1-PROPANOL
BOC-(S)-2-AMINO-3-PHENYLMETHOXY-1-PROPANOL
BOC-SER(BZL)-OL
BOC-SERINOL(BZL)
N-ALPHA-T-BOC-O-BENZYL-D-SERINOL
N-ALPHA-T-BOC-O-BENZYL-L-SERINOL
N-BOC-D-SER(BZL)-OL
N-BOC-D-SER(BZL)-OLN-BOC-(S)-2-AMINO-3-BENZYLOXY-1-PROPANOL
N-BOC-L-SER(BZL)-OL
N-BOC-L-SER(BZL)-OL-N-BOC-(R)-2-AMINO-3-BENZYLOXY-1-PROPANOL
N-BOC-(R)-2-AMINO-3-BENZYLOXY-1-PROPANOL
N-T-BUTOXYCARBONYL-O-BENZYL-D-SERINOL
N-T-BUTOXYCARBONYL-O-BENZYL-L-SERINOL
(R)-(+)-3-BENZYLOXY-2-(TERT-BUTOXYCARBONYLAMINO)-1-PROPANOL
N-BOC-(S)-2-AMINO-3-BENZYLOXY-1-PROPANOL
N-alpha-t-Butyloxycarbonyl-O-benzyl-D-serinol
[Molecular Formula]

C15H23NO4
[MDL Number]

MFCD00235944
[Molecular Weight]

281.35
[MOL File]

79069-15-1.mol
Chemical PropertiesBack Directory
[Melting point ]

66-69 °C(lit.)
[alpha ]

-14 º (c=1 in chloroform)
[Boiling point ]

443.1±40.0 °C(Predicted)
[density ]

1.105
[storage temp. ]

Store at 0-5°C
[solubility ]

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
[form ]

Powder
[pka]

11.58±0.46(Predicted)
[InChI]

InChI=1S/C15H23NO4/c1-15(2,3)20-14(18)16-13(9-17)11-19-10-12-7-5-4-6-8-12/h4-8,13,17H,9-11H2,1-3H3,(H,16,18)/t13-/m0/s1
[InChIKey]

MSIDLARYVJJEQY-ZDUSSCGKSA-N
[SMILES]

C(OC(C)(C)C)(=O)N[C@@H](CO)COCC1=CC=CC=C1
[CAS DataBase Reference]

79069-15-1(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302+H312+H332-H315
[Precautionary statements ]

P280-P301+P312-P362+P364
[WGK Germany ]

3
[HS Code ]

2924297099
Hazard InformationBack Directory
[Chemical Properties]

White to off-white solid
[Synthesis]

Under an atmosphere of argon, to a solution of 2,5-dioxopyrrolidin-1-yl O-benzyl-N-t-butoxycarbonyl-L-serinate (4.41 g) in tetrahydrofuran(30 mL) was added sodium borohydride (644 mg) in ice bath and the mixture was stirred at room temperature overnight. Water was added to the reaction solution, which was extracted with ethyl acetate. The organic layer was washed with an aqueous saturated ammonium chloride solution and brine, dried over anhydrous magnesium sulfate, and concentrated to give N-Boc-(S)-2-amino-3-benzyloxy-1-propanol.
N-Boc-(S)-2-amino-3-benzyloxy-1-propanol
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