Borane products
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- Borane compound-reducing agent
- Borane dimethyl sulfide complex
- Borane tetrahydrofuran complex
- (+)-B-Chlorodiisopinocampheylborane
- (-)-B-Chlorodiisopinocampheylborane
- N,N-Diethylaniline borane
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- Borane-N,N-diisopropylethylamine complex
- Dibromoborane dimethyl sulfide complex
- Borane compound-catalyst
- (R)-Methyl Oxazaborolidine
- (S)-Methyl Oxazaborolidine
- (R)-(+)-2-(Diphenylhydroxymethyl)pyrrolidine
- (S)-(-)-2-(Diphenylhydroxymethyl)pyrrolidine
- Borane Compound-Coupling Reagent
- Pinacolborane
- Catecholborane
- Methoxydiethylborane
- Diethyl(3-pyridyl)borane
- 9-Borabicyclo[3.3.1]nonane solution
- B-Methoxy-9-borabicyclo[3.3.1]nonane
- Trimethyl boroxine
- Methyl boronic acid
- Chiral Compound
- (R)-(+)-1-Phenylethanol
- (S)-(-)-1-Phenylethanol
- (R)-1-(3,5-Bis-trifluoromethylphenyl)ethanol
- (S)-1-(3,5-Bis-trifluoromethylphenyl)ethanol
- (1R,2R,3S,5R)-(-)-2,3-Pinanediol
- (1S,2S,3R,5S)-(+)-2,3-Pinanediol
- (1S,2S,5S)-(-)-2-Hydroxy-3-pinanone
- (1R,2R,5R)-(+)-2-Hydroxy-3-pinanone
- (R)-Styrene oxide
- (S)-Styrene oxide
- (R)-1-(4-Bromophenyl)ethanol
- (S)-1-(4-Bromophenyl)ethanol
- (R)-(4-Chlorophenyl)oxirane
- (S)-(4-Chlorophenyl)oxirane
- (R)-2-(1-Hydroxyethyl) pyridine
- (S)-2-(1-Hydroxyethyl) pyridine
- (R)-4-(1-Hydroxyethyl) pyridine
- (S)-4-(1-Hydroxyethyl) pyridine
- (R)-(3-Chlorophenyl)oxirane
- (R)-(4-Fluorophenyl)oxirane
- (R)-(+)-1-(1-Naphthyl)ethanol
- (S)-(−)-1-(1-Naphthyl)ethanol
- Others
- Methylindole
- 2,4-Dichloropyrimidine
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(S)-(-)-1-Phenylethanol
【Catalog Number】CR8010
【CAS #】1445-91-6
【Molecular Formula】C8H10O
【Molecular Weight】122.16
English Name :
(S)-(-)-1-Phenylethanol
CAS# :
1445-91-6
产品描述
Parameters
|
Alias |
D-1-phenylethanol; (S)-(-)-1-phenylethanol |
|
Catalog Number |
CR8010 |
|
CAS # |
1445-91-6 |
|
Molecular Formula |
C8H10O |
|
Molecular Weight |
122.16 |
|
Structural Formula |
|
|
Product Introduction CAS 1445-91-6 |
(S)-(-)-1-phenylethanol, the English name is, American Chemical Abstracts Registration Number is cas 1445-91-6. This product (cas 1445-91-6) is an intermediate for pharmaceutical synthesis. The alcoholic hydroxyl group in the molecular structure can further undergo substitution reactions with other acyl, amino, halide, etc. For the synthesis of chiral drugs. |
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