(S)-Baclofen hydrochloride structure
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Common Name | (S)-Baclofen hydrochloride | ||
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CAS Number | 63701-56-4 | Molecular Weight | 250.12200 | |
Density | N/A | Boiling Point | 364.3ºC at 760mmHg | |
Molecular Formula | C10H13Cl2NO2 | Melting Point | 223 - 224 °C | |
MSDS | USA | Flash Point | 174.1ºC |
Name | (3S)-4-amino-3-(4-chlorophenyl)butanoic acid,hydrochloride |
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Synonym | More Synonyms |
Boiling Point | 364.3ºC at 760mmHg |
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Melting Point | 223 - 224 °C |
Molecular Formula | C10H13Cl2NO2 |
Molecular Weight | 250.12200 |
Flash Point | 174.1ºC |
Exact Mass | 249.03200 |
PSA | 63.32000 |
LogP | 3.35930 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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RIDADR | UN 2811 6.1/PG 3 |
RTECS | MW5084400 |
Effects of phaclofen and the enantiomers of baclofen on cardiovascular responses to intrathecal administration of L- and D-baclofen in the rat.
Eur. J. Pharmacol. 196 , 267, (1991) In a previous study it was found that i.t. administration of L-baclofen decreased arterial pressure and heart rate while D-baclofen differentially increased arterial pressure. The objective of the pre... |
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Comparative stereostructure-activity studies on GABAA and GABAB receptor sites and GABA uptake using rat brain membrane preparations.
J. Neurochem. 47 , 898, (1986) The affinities of a number of analogues of gamma-aminobutyric acid (GABA) for GABAA and GABAB receptor sites and GABA uptake were studied using rat brain membrane preparations. Studies on the (S)-(+)-... |
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3-(p-Chlorophenyl)-4-aminobutanoic acid--resolution into enantiomers and pharmacological activity.
Pol. J. Pharmacol. Pharm. 32 , 187, (1980) Racemic 3-(p-chlorophenyl)-4-aminobutanoic acid was resolved into enantiomers and their absolute configuration determined. Pharmacological activity of hydrochlorides of the racemic acid and its enanti... |
UNII-799SU69U5P |
S(-)-Baclofen hydrochloride |
(-)-Baclofen hydrochloride |
l-Baclofen hydrochloride |
(-)-S-3-(p-Chlorophenyl)-4-aminobutanoic acid hydrochloride |