N-methoxy-2-(2-methoxy-4-prop-2-enylphenoxy)-N-methylacetamide

Names

[ CAS No. ]:
92501-70-7

[ Name ]:
N-methoxy-2-(2-methoxy-4-prop-2-enylphenoxy)-N-methylacetamide

Chemical & Physical Properties

[ Molecular Formula ]:
C14H19NO4

[ Molecular Weight ]:
265.30500

[ Exact Mass ]:
265.13100

[ PSA ]:
48.00000

[ LogP ]:
1.82230

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
AK8167000
CHEMICAL NAME :
Acetohydroxamic acid, 2-(4-allyl-2-methoxyphenoxy)-N,O-dimethyl-
CAS REGISTRY NUMBER :
92501-70-7
LAST UPDATED :
199612
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C14-H19-N-O4
MOLECULAR WEIGHT :
265.34
WISWESSER LINE NOTATION :
1U2R CO1 DO1VN1&O1

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 :
1745 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 :
625 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 :
85 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

  • 3-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-phenylacetamido]-2-hydroxy-2-methylpropanoic acid
  • 2-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-phenyl-N-(prop-2-yn-1-yl)acetamido]acetic acid
  • 2-Methyl-2-(2-methyloxolan-3-yl)propan-1-ol
  • 5-[(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-methylpentanamido]pyridine-3-carboxylic acid
  • 3-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pyridine-2-amido]cyclopentane-1-carboxylic acid
  • 2-({[3-ethoxy-1-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylcyclobutyl]formamido}oxy)acetic acid
  • 3-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-methanesulfonylbutanamido]-2-methylpropanoic acid
  • 2-cyclopropyl-2-{[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-1H-1,2,4-triazol-3-yl]formamido}propanoic acid
  • 4-{1-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-methyl-1,3-thiazol-5-yl]-N-methylformamido}butanoic acid
  • 1-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-1,2,5-oxadiazole-3-carbonyl]-3-methylpyrrolidine-3-carboxylic acid
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