710-77-0

710-77-0 structure
710-77-0 structure
  • Name: Barbituric acid, 5-ethyl-5-(2-hydroxyethyl)-
  • Chemical Name: 5-ethyl-5-(2-hydroxyethyl)-1,3-diazinane-2,4,6-trione
  • CAS Number: 710-77-0
  • Molecular Formula: C8H12N2O4
  • Molecular Weight: 200.19200
  • Create Date: 2016-12-24 02:30:55
  • Modify Date: 2024-03-02 11:39:04

Name 5-ethyl-5-(2-hydroxyethyl)-1,3-diazinane-2,4,6-trione
Synonyms 5-Aethyl-5-(2-hydroxy-aethyl)-barbitursaeure
5-ethyl-5-(2-hydroxyethyl)pyrimidine-2,4,6(1h,3h,5h)-trione
5-Ethyl-5-(2-hydroxyethyl)barbituric acid
Barbituric acid,5-ethyl-5-(2-hydroxyethyl)
2,4,6(1H,3H,5H)-Pyrimidinetrione,5-ethyl-5-(2-hydroxyethyl)
5-ethyl-5-(2-hydroxyethyl)-2,4,6(1H,3H,5H)-pyrimidinetrione
Molecular Formula C8H12N2O4
Molecular Weight 200.19200
Exact Mass 200.08000
PSA 95.50000

CHEMICAL IDENTIFICATION

RTECS NUMBER :
CQ4932000
CHEMICAL NAME :
Barbituric acid, 5-ethyl-5-(2-hydroxyethyl)-
CAS REGISTRY NUMBER :
710-77-0
BEILSTEIN REFERENCE NO. :
0195143
LAST UPDATED :
199612
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C8-H12-N2-O4
MOLECULAR WEIGHT :
200.22

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>4 gm/kg
TOXIC EFFECTS :
Behavioral - somnolence (general depressed activity)
REFERENCE :
AITEAT Archivum Immunologiae et Therapiae Experimentalis. (Ars Polona, POB 1001, 00-068 Warsaw 1, Poland) V.10- 1962- Volume(issue)/page/year: 14,662,1966

~69%

710-77-0 structure

710-77-0

Literature: Lafont; Chastang; Cave; Miocque European Journal of Medicinal Chemistry, 1988 , vol. 23, # 3 p. 283 - 289

~%

710-77-0 structure

710-77-0

Literature: Goldschmidt; Wehr Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, 1957 , vol. 308, p. 9,15

~%

710-77-0 structure

710-77-0

Literature: Goldschmidt; Wehr Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, 1957 , vol. 308, p. 9,15

~74%

710-77-0 structure

710-77-0

Literature: Lafont; Chastang; Cave; Miocque European Journal of Medicinal Chemistry, 1988 , vol. 23, # 3 p. 283 - 289