N-methoxy-N-methyl-2-(2-methyl-5-propan-2-ylphenoxy)acetamide

Names

[ Name ]:
N-methoxy-N-methyl-2-(2-methyl-5-propan-2-ylphenoxy)acetamide

[Synonym ]:
2-Carvacryloxy-N,O-dimethylacetohydroxamic acid
ACETOHYDROXAMIC ACID,2-CARVACRYLOXY-N,O-DIMETHYL
<2-Methyl-5-isopropyl-phenoxy>-essigsaeure-<N-methoxy-N-methyl-amid>

Chemical & Physical Properties

[ Density]:
1.046g/cm3

[ Boiling Point ]:
333.4ºC at 760mmHg

[ Molecular Formula ]:
C₁₄H₂₁NO₃

[ Molecular Weight ]:
251.32100

[ Flash Point ]:
155.4ºC

[ Exact Mass ]:
251.15200

[ PSA ]:
38.77000

[ LogP ]:
2.51700

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :: AK8316300

CHEMICAL NAME :: Acetohydroxamic acid, 2-carvacryloxy-N,O-dimethyl-

CAS REGISTRY NUMBER :: 97282-05-8

LAST UPDATED :: 199612

DATA ITEMS CITED :: 3

MOLECULAR FORMULA :: C14-H21-N-O3

MOLECULAR WEIGHT :: 251.36

WISWESSER LINE NOTATION :: 1ON1&V1OR B1 EY1&1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Oral

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 1678 mg/kg

TOXIC EFFECTS :: Behavioral - somnolence (general depressed activity)

REFERENCE :: JMPCAS Journal of Medicinal and Pharmaceutical Chemistry. (Washington, DC) V.1-5, 1959-62. For publisher information, see JMCMAR. Volume(issue)/page/year: 4,317,1961

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intraperitoneal

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 733 mg/kg

TOXIC EFFECTS :: Behavioral - somnolence (general depressed activity)

REFERENCE :: JMPCAS Journal of Medicinal and Pharmaceutical Chemistry. (Washington, DC) V.1-5, 1959-62. For publisher information, see JMCMAR. Volume(issue)/page/year: 4,317,1961

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intravenous

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 82 mg/kg

TOXIC EFFECTS :: Behavioral - somnolence (general depressed activity)

REFERENCE :: JMPCAS Journal of Medicinal and Pharmaceutical Chemistry. (Washington, DC) V.1-5, 1959-62. For publisher information, see JMCMAR. Volume(issue)/page/year: 4,317,1961

Synthetic Route

Click to get detail synthetic route

Related Compounds

N-((1r,4r)-4-(pyridin-2-yloxy)cyclohexyl)isoxazole-5-carboxamide
2-methyl-N-((1r,4r)-4-(pyridin-2-yloxy)cyclohexyl)thiazole-4-carboxamide
1-methyl-6-oxo-N-((1r,4r)-4-(pyridin-2-yloxy)cyclohexyl)-1,6-dihydropyridazine-3-carboxamide
3-(3,5-dimethylisoxazol-4-yl)-N-((1r,4r)-4-(pyridin-2-yloxy)cyclohexyl)propanamide
3-(4-oxoquinazolin-3(4H)-yl)-N-((1r,4r)-4-(pyridin-2-yloxy)cyclohexyl)propanamide
2-(4-oxoquinazolin-3(4H)-yl)-N-((1r,4r)-4-(pyridin-2-yloxy)cyclohexyl)acetamide
1-acetyl-N-((1r,4r)-4-(pyridin-2-yloxy)cyclohexyl)piperidine-4-carboxamide
2-methoxy-N-((1r,4r)-4-(pyridin-2-yloxy)cyclohexyl)acetamide
2-ethoxy-N-((1r,4r)-4-(pyridin-2-yloxy)cyclohexyl)acetamide
N-((1r,4r)-4-(pyridin-2-yloxy)cyclohexyl)-2-(thiophen-2-yl)acetamide

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