esatenolol

Modify Date: 2024-01-09 18:17:27

esatenolol Structure
esatenolol structure
Common Name esatenolol
CAS Number 93379-54-5 Molecular Weight 266.33600
Density 1.125 g/cm3 Boiling Point 508ºC at 760mmHg
Molecular Formula C14H22N2O3 Melting Point 148-152 ºC(lit.)
MSDS USA Flash Point 261.1ºC

 Names

Name esatenolol
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.125 g/cm3
Boiling Point 508ºC at 760mmHg
Melting Point 148-152 ºC(lit.)
Molecular Formula C14H22N2O3
Molecular Weight 266.33600
Flash Point 261.1ºC
Exact Mass 266.16300
PSA 84.58000
LogP 1.54330

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
CY1488020
CHEMICAL NAME :
Benzeneacetamide, 4-(2-hydroxy-3-((1-methylethyl)amino)propoxy)-, (S)-
CAS REGISTRY NUMBER :
93379-54-5
LAST UPDATED :
199403
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C14-H22-N2-O3
MOLECULAR WEIGHT :
266.38

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
97 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
PIXXD2 PCT (Patent Cooperation Treaty) International Application. (U.S. Patent and Trademark Office, Foreign Patents, Washington, DC 20231) Volume(issue)/page/year: #91-10428

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS CY1488020
HS Code 2924299090

 Synthetic Route

 Customs

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles5

More Articles
Chemical genetics reveals a complex functional ground state of neural stem cells.

Nat. Chem. Biol. 3(5) , 268-273, (2007)

The identification of self-renewing and multipotent neural stem cells (NSCs) in the mammalian brain holds promise for the treatment of neurological diseases and has yielded new insight into brain canc...

Effects of nebivolol on endothelial gene expression during oxidative stress in human umbilical vein endothelial cells.

Mediators Inflamm. 2008 , 367590, (2008)

The endothelium plays a key role in the development of atherogenesis and its inflammatory and proliferative status influences the progression of atherosclerosis. The aim of this study is to compare th...

The effects of (+/-)-, (+)-, and (-)-atenolol, sotalol, and amosulalol on the rat left atria and portal vein.

Chirality 5 , 8-14, (1993)

The effects of (+/-)-, (+)-, and (-)-atenolol, sotalol, and amosulalol alone on the rat left atria and portal vein and on the respective beta 1- and beta 2-adrenoceptor-mediated responses to isoprenal...

 Synonyms

(-)-4-[2-hydroxy-3-[(1-methylethyl)amino]propoxy]benzeneacetamide
S-(-)-Atenolol
(S)-4-[2-hydroxy-3-((1-methylethyl)amino)propoxy]benzeneacetamide
MFCD00074918
(-)-Atenolol
1-Phenylbiguanide hydrochloride
2-[4-[(2S)-2-hydroxy-3-(propan-2-ylamino)propoxy]phenyl]acetamide
Esatenolol [INN]
4-{(2S)-2-hydroxy-3-[(1-methylethyl)amino]propoxy}benzeneacetamide
Esatenolol
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