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2(3H)-Benzothiazolone, 5-chloro-3-[2-[4-(2-hydroxyethyl)-1-piperazinyl]-2-oxoethyl]-, hydrochloride (1:1)

2(3H)-Benzothiazolone, 5-chloro-3-[2-[4-(2-hydroxyethyl)-1-piperazinyl]-2-oxoethyl]-, hydrochloride (1:1) structure

CAS No:
35941-71-0
Formula:
C15H18ClN3O3S.ClH
Chemical Name:
2(3H)-Benzothiazolone, 5-chloro-3-[2-[4-(2-hydroxyethyl)-1-piperazinyl]-2-oxoethyl]-, hydrochloride (1:1)
Synonyms:
2(3H)-Benzothiazolone,5-chloro-3-[2-[4-(2-hydroxyethyl)-1-piperazinyl]-2-oxoethyl]-,hydrochloride (1:1);1-Piperazineethanol,4-[(5-chloro-2-oxo-3(2H)-benzothiazolyl)acetyl]-,monohydrochloride;Tiaramide hydrochloride;Solantal;RHC 2592;FK 1160;NTA 194;NSC 289337

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Description

Tiaramide hydrochloride is a member of benzothiazoles.

2(3H)-Benzothiazolone, 5-chloro-3-[2-[4-(2-hydroxyethyl)-1-piperazinyl]-2-oxoethyl]-, hydrochloride (1:1) Basic Attributes

Molecular Weight：

392.30066

Exact Mass：

391.052429

EC Number：

252-802-7

UNII：

ITY1616X9T

NSC Number：

289337

DSSTox ID：

DTXSID6048757

Characteristics

PSA：

89.4

XLogP3：

1.53070

Melting Point：

159-161 °C

Toxicity：

Oral-Rat LD50: 2300 mg/kg; Oral-Mouse LD50: 560 mg/kg

Flammability characteristics：

Combustible, decomposes toxic chloride, sulfur oxide and nitrogen oxide gas when burning

Safety Information

RTECS Number：

TL7050000

Storage features：

Warehouse low temperature, ventilated, dry

Precautionary statement(s)：

P264, P280, P305+P351+P338, P33, P313

Hazard Statements：

H319

GHS Classification：

|Warning|H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]|P264, P280, P305+P351+P338, and P337+P313|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Toxicity

Toxicity class：

moderately toxic

Drug Information

MeSH：

Agents that cause an increase in the expansion of a bronchus or bronchial tubes. (See all compounds classified as Bronchodilator Agents.)|Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)

MeSH Entry Terms：

FK 1160

Computed Properties

Molecular Weight:392.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:391.0524180
Monoisotopic Mass:391.0524180
Topological Polar Surface Area:89.4
Heavy Atom Count:24
Complexity:459
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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2(3H)-Benzothiazolone, 4-hydroxy-7-[2-[[2-[[3-(2-phenylethoxy)propyl]sulfonyl]ethyl]amino]ethyl]-, hydrochloride (1:1)

154189-24-9

Hot Searches: carbon monoxide formula; h3bo3; sodium amytal; benzyl acetate; methanol molecular formula; nitrogen trioxide

Guide of 2(3H)-Benzothiazolone, 5-chloro-3-[2-[4-(2-hydroxyethyl)-1-piperazinyl]-2-oxoethyl]-, hydrochloride (1:1)

Description
Basic Attributes
Characteristics
Safety Information
Toxicity
Drug Information
Computed Properties
Learn More Other Chemicals

2(3H)-Benzothiazolone, 5-chloro-3-[2-[4-(2-hydroxyethyl)-1-piperazinyl]-2-oxoethyl]-, hydrochloride (1:1)

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