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N-Benzoyl-(2R,3S)-3-phenylisoserine_Molecular_structure_CAS_132201-33-3)
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N-Benzoyl-(2R,3S)-3-phenylisoserine

Catalog No. 444375 Name Sigma Aldrich
CAS Number 132201-33-3 Website http://www.sigmaaldrich.com
M. F. C16H15NO4 Telephone 1-800-521-8956
M. W. 285.2946 Fax
Purity 98% Email
Storage Chembase ID: 146887

SYNONYMS

Title
N-苯甲酰基-(2R,3S)-3-苯基异丝氨酸
IUPAC name
(2R,3S)-2-hydroxy-3-phenyl-3-(phenylformamido)propanoic acid
IUPAC Traditional name
(2R,3S)-2-hydroxy-3-phenyl-3-(phenylformamido)propanoic acid

DATABASE IDS

PubChem SID 24868119
MDL Number MFCD00274633
CAS Number 132201-33-3

PROPERTIES

Linear Formula C6H5CONHCH(C6H5)CH(OH)CO2H
Purity 98%
Melting Point 169-172 °C(lit.)
Optical Rotation [α]20/D -40°, c = 1.0 in ethanol
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Packaging
500 mg in glass bottle
Application
The presence of this chiral side chain has proven to be essential for the biological activity of taxol,1,2,3 one of the most promising anticancer agents being investigated.4,5 The challenging synthesis of taxol has stimulated interest in the attachment of the C-13 side chain to naturally derived taxanes like baccatin III.6,7,8
Description (简体中文)
包装
500 mg in glass bottle
Application
已经证明,该手性侧链的存在对于紫杉醇的生物活性至关重要,1,2,3 紫杉醇是目前正在研究的最有潜力的抗癌药之一。4,5 紫杉醇复杂的合成过程已经引起人们对在天然衍生紫杉烷类(例如,巴卡亭 III)上附接 C-13 侧链的关注。6,7,8

REFERENCES