Borane products
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- (+)-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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(R)-4-(1-Hydroxyethyl) pyridine
【Catalog Number】CR8017
【CAS #】27854-88-2
【Molecular Formula】C7H9NO
【Molecular Weight】123.15
English Name :
(R)-4-(1-Hydroxyethyl) pyridine
CAS# :
27854-88-2
产品描述
Parameters
|
Alias |
(R)-(+)-α-methyl-4-pyridinemethanol |
|
Catalog Number |
CR8017 |
|
CAS # |
27854-88-2 |
|
Molecular Formula |
C7H9NO |
|
Molecular Weight |
123.15 |
|
Structural Formula |
|
|
Product Introduction CAS 27854-88-2 |
(R) -4-hydroxyethylpyridine. The English name is (R) -4- (1-Hydroxyethyl) pyridine, and the American Chemical Abstracts Registration Number is cas27854-88-2. This product (cas 27854-88-2) 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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