Chlormezanone structure, CAS 80-77-3

Chlormezanone

CAS Number80-77-3

SynonymsSuprotan; (±)-Chlormezanone; Transanate; 2-(4-Chlorophenyl)tetrahydro-3-methyl-4H-1,3-thiazin-4-one 1,1-dioxide; UNII:GP568V9G19; 2-(p-Chlorophenyl)perhydro-3-methyl-1,3-thiazin-4-one 1,1-Dioxide; 2-(4-chlorophenyl)-3-methyl-1,1-dioxo-1,3-thiazinan-4-one; Lobak; MFCD00143951; chlormezanone; 4H-1,3-Thiazin-4-one, 2-(4-chlorophenyl)tetrahydro-3-methyl-, 1,1-dioxide; 2-(4-Chlorophenyl)-3-methyl-1,3-thiazinan-4-one 1,1-dioxide; Dichloromethazanone; UNII:C14WB33Y0S; 2-(4-Chlorophenyl)-3-methyl-4-metathiazanone 1,1-Dioxide; 4H-1,3-Thiazin-4-one, 2- (4-chlorophenyl)tetrahydro-3-methyl-, 1,1-dioxide; UNII:4BU37OM8KL; EINECS 201-307-4

Molecular FormulaC11H12O3N1Cl1S1

Molecular Weight273.74

Purity98.00%

Density1.4±0.1 g/cm3

Boiling Point534.5±50.0 °C at 760 mmHg

Melting Point114ºC

Flash Point

Appearance

EINECS

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Cat. No.: 2A-9017325 Purity: 98.00%
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Quality Control of [ 80-77-3 ] Purity: 98.00% SDS Specification MoL

Chemical & Physical Properties
CAS Number80-77-3
Catalog No.2A-9017325
Chinese Name氯美扎酮
SynonymsSuprotan; (±)-Chlormezanone; Transanate; 2-(4-Chlorophenyl)tetrahydro-3-methyl-4H-1,3-thiazin-4-one 1,1-dioxide; UNII:GP568V9G19; 2-(p-Chlorophenyl)perhydro-3-methyl-1,3-thiazin-4-one 1,1-Dioxide; 2-(4-chlorophenyl)-3-methyl-1,1-dioxo-1,3-thiazinan-4-one; Lobak; MFCD00143951; chlormezanone; 4H-1,3-Thiazin-4-one, 2-(4-chlorophenyl)tetrahydro-3-methyl-, 1,1-dioxide; 2-(4-Chlorophenyl)-3-methyl-1,3-thiazinan-4-one 1,1-dioxide; Dichloromethazanone; UNII:C14WB33Y0S; 2-(4-Chlorophenyl)-3-methyl-4-metathiazanone 1,1-Dioxide; 4H-1,3-Thiazin-4-one, 2- (4-chlorophenyl)tetrahydro-3-methyl-, 1,1-dioxide; UNII:4BU37OM8KL; EINECS 201-307-4
Molecular FormulaC11H12O3N1Cl1S1
Molecular Weight273.74
Purity98.00
Density1.4±0.1 g/cm3
Boiling Point534.5±50.0 °C at 760 mmHg
Melting Point114ºC
Storage ConditionStore at RT
ApplicationChlormezanone is similar to benzodiazepines. Chlormezanone works similarly to benzodiazepines. Chlormezanone is used as an anxiolytic and muscle relaxant.
MDL NumberMFCD00143951
SMILESCN1C(=O)CCS(=O)(=O)C1c1ccc(Cl)cc1
InChIInChI=1S/C11H12ClNO3S/c1-13-10(14)6-7-17(15,16)11(13)8-2-4-9(12)5-3-8/h2-5,11H,6-7H2,1H3
InChI KeyWEQAYVWKMWHEJO-UHFFFAOYSA-N
MSDSmsds/17325_1_80_77_3.pdf
BioactivityChlormezanone resembles benzodiazepine. The action of Chlormezanone is similar to benzodiazepine-type agents. Chlormezanone is used as an anxiolytic and a muscle relaxant. Related Catalog Signaling Pathways >> Membrane Transporter/Ion Channel >> GABA Receptor Signaling Pathways >> Neuronal Signaling >> GABA Receptor Research Areas >> Neurological Disease Target Benzodiazepine[1] In Vivo Comparative results obtained with Chlormezanone in the dosage levels capable of producing more than 80% depression in the contralateral extensor[1]. Animal Admin Cats[1] Effects of various agents (e.g., Chlormezanone 300 mg/kg i.p.) are studied on linguomandibular, extensor and patellar reflexes in spinal cats. References [1]. Sukehiro CHIBA, et al. EFFECTS OF NEW s-TRIAZOLOBENZODIAZEPINE (D-4OTA) AND OTHER CENTRAL MUSCLE RELAXANTS ON SPINAL AND SUPRASPINAL REFLEXES IN CATS. Japan. J. Pharmacol, 23, 83-96 (1973). Chemical & Physical Properties Density 1.4±0.1 g/cm3 Boiling Point 534.5±50.0 °C at 760 mmHg Melting Point 114ºC Molecular Formula C11H12ClNO3S Molecular Weight 273.736 Flash Point 277.1±30.1 °C Exact Mass 273.022644 PSA 62.83000 LogP 0.86 Vapour Pressure 0.0±1.4 mmHg at 25°C Index of Refraction 1.580 InChIKey WEQAYVWKMWHEJO-UHFFFAOYSA-N SMILES CN1C(=O)CCS(=O)(=O)C1c1ccc(Cl)cc1 Storage condition Store at RT
Use ofChlormezanone resembles benzodiazepine. The action of Chlormezanone is similar to benzodiazepine-type agents. Chlormezanone is used as an anxiolytic and a muscle relaxant. Properties Name chlormezanone Synonym More Synonyms chlormezanone Biological Activity Description Chlormezanone resembles benzodiazepine. The action of Chlormezanone is similar to benzodiazepine-type agents. Chlormezanone is used as an anxiolytic and a muscle relaxant. Related Catalog Signaling Pathways >> Membrane Transporter/Ion Channel >> GABA Receptor Signaling Pathways >> Neuronal Signaling >> GABA Receptor Research Areas >> Neurological Disease Benzodiazepine[1] In Vivo Comparative results obtained with Chlormezanone in the dosage levels capable of producing more than 80% depression in the contralateral extensor[1]. References [1]. Sukehiro CHIBA, et al. EFFECTS OF NEW s-TRIAZOLOBENZODIAZEPINE (D-4OTA) AND OTHER CENTRAL MUSCLE RELAXANTS ON SPINAL AND SUPRASPINAL REFLEXES IN CATS. Japan. J. Pharmacol, 23, 83-96 (1973). Chemical & Physical Properties Exact Mass 273.022644 PSA 62.83000 Index of Refraction 1.580 InChIKey WEQAYVWKMWHEJO-UHFFFAOYSA-N Storage condition Store at RT
Transport InfoProduct name: Purity: 98.0%
MSDS Transport InfoModule 14. Shipping information United Nations classification: inconsistent with United Nations classification standards UN number: not specified Fenalu
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