368199
(S)-(−)-α,α-Diphenyl-2-pyrrolidinemethanol
99%
Synonym(s):
(S)-(−)-2-(Diphenylhydroxymethyl)pyrrolidine, α,α-Diphenyl-L-prolinol
About This Item
Recommended Products
Quality Level
Assay
99%
form
solid
optical activity
[α]20/D −67°, c = 3 in chloroform
mp
77-80 °C (lit.)
functional group
hydroxyl
phenyl
SMILES string
OC([C@@H]1CCCN1)(c2ccccc2)c3ccccc3
InChI
1S/C17H19NO/c19-17(16-12-7-13-18-16,14-8-3-1-4-9-14)15-10-5-2-6-11-15/h1-6,8-11,16,18-19H,7,12-13H2/t16-/m0/s1
InChI key
OGCGXUGBDJGFFY-INIZCTEOSA-N
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General description
Application
- DPPM reacts with catecholborane to form a spiroborate ester, which can be an efficient catalyst for the synthesis of enantiopure alcohols by borane reduction of acetophenone.
- The catalyst generated in situ by reacting DPPM with borane-diethylaniline, can efficiently catalyze the enantioselective reduction of 2′-fluoroacetophenone.
- Mesoporous SBA-15 silica functionalized with DPPM can catalyze the addition of diethylzinc to benzaldehyde to form (S)-1-phenyl-propanol.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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