3483-14-5

3483-14-5 structure
3483-14-5 structure
  • Name: N-(Butyl)-sydonimin hydrochlorid [German]
  • Chemical Name: 5-amino-3-bromoindazole
  • CAS Number: 3483-14-5
  • Molecular Formula: C6H12ClN3O
  • Molecular Weight: 177.63200
  • Create Date: 2016-05-25 00:18:47
  • Modify Date: 2024-03-10 17:23:05

Name 5-amino-3-bromoindazole
Synonyms 3-butylsydnonimine hydrochorid
3-bromo-1H-indazole-5-ylamine
3-bromo-1H-indazol-5-ylamine
3-bromo-1H-indazol-5-amine
3-butylsydnonimine hydrochloride
1H-Indazol-5-amine,3-bromo
Molecular Formula C6H12ClN3O
Molecular Weight 177.63200
Exact Mass 177.06700
PSA 41.94000
LogP 2.24790

CHEMICAL IDENTIFICATION

RTECS NUMBER :
WU7677320
CHEMICAL NAME :
Sydnone imine, 3-butyl-, monohydrochloride
CAS REGISTRY NUMBER :
3483-14-5
LAST UPDATED :
198511
DATA ITEMS CITED :
2
MOLECULAR FORMULA :
C6-H11-N3-O.Cl-H
MOLECULAR WEIGHT :
177.66
WISWESSER LINE NOTATION :
T5NNOYJ A4 DUM &GH

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 :
230 mg/kg
TOXIC EFFECTS :
Autonomic Nervous System - smooth muscle relaxant (mechanism undefined, spasmolytic) Behavioral - anticonvulsant Behavioral - altered sleep time (including change in righting reflex)
REFERENCE :
ABMGAJ Acta Biologica et Medica Germanica. (Berlin, Ger. Dem. Rep.) V.1-41, 1958-82. For publisher information, see BBIADT. Volume(issue)/page/year: 14,369,1965
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
125 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 2,280,1968

~%

3483-14-5 structure

3483-14-5

Literature: Beal; Turnbull Synthetic Communications, 1992 , vol. 22, # 5 p. 673 - 676

~%

3483-14-5 structure

3483-14-5

Literature: Beal; Turnbull Synthetic Communications, 1992 , vol. 22, # 5 p. 673 - 676
Precursor  2

DownStream  0