Hydrohydrastinine, hydrochloride

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Names

[ CAS No. ]:
5985-04-6

[ Name ]:
Hydrohydrastinine, hydrochloride

[Synonym ]:
6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinoline,hydrochloride
hydrohydrastinine hydrochloride
6-Methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isochinolin,Hydrochlorid
dihydrohydrastinin,hydrochloride

Chemical & Physical Properties

[ Boiling Point ]:
304ºC at 760 mmHg

[ Molecular Formula ]:
C11H14ClNO2

[ Molecular Weight ]:
227.68700

[ Flash Point ]:
123ºC

[ Exact Mass ]:
227.07100

[ PSA ]:
21.70000

[ LogP ]:
2.14310

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
JI4870000
CHEMICAL NAME :
1,3-Dioxolo(4,5-g)isoquinoline, 5,6,7,8-tetrahydro-6-methyl-, hydrochloride
CAS REGISTRY NUMBER :
5985-04-6
LAST UPDATED :
199712
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C11-H13-N-O2.Cl-H
MOLECULAR WEIGHT :
227.71
WISWESSER LINE NOTATION :
T C566 DO FO KN EH&&TJ K1 &GH

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Parenteral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
150 mg/kg
TOXIC EFFECTS :
Behavioral - somnolence (general depressed activity) Behavioral - convulsions or effect on seizure threshold Behavioral - muscle contraction or spasticity
REFERENCE :
JPETAB Journal of Pharmacology and Experimental Therapeutics. (Williams & Wilkins Co., 428 E. Preston St., Baltimore, MD 21202) V.1- 1909/10- Volume(issue)/page/year: 62,165,1938

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Formaldehyde
  • 5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinoline

DownStream

Related Compounds

  • Tyrocidine, hydrochloride
  • Triprolidine hydrochloride
  • Minoxidil hydrochloride
  • Elacridar hydrochloride
  • dodecylamine hydrochloride
  • Azetidine, hydrochloride, homopolymer (9CI)
  • 3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-hydroxybutanoic acid
  • 1-(3,4-dihydroquinolin-1(2H)-yl)-2-(3-(3-(3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-5-yl)azetidin-1-yl)ethanone oxalate
  • Tryptophan,n-acetyl-7-(phenylmethoxy)-
  • 1h-Pyrazolo[4,3-c]pyridine,3-(4-ethoxyphenyl)-4,5,6,7-tetrahydro-1-(phenylmethyl)-,hydrochloride
  • 1h-Pyrazolo[4,3-c]pyridine,3-(4-ethoxyphenyl)-4,5,6,7-tetrahydro-5-methyl-1-(phenylmethyl)-,monomethanesulfonate
  • 1h-Pyrazolo[4,3-c]pyridine,3-(4-fluorophenyl)-4,5,6,7-tetrahydro-1-(1-methylethyl)-,monomethanesulfonate
  • 1h-Pyrrolo[2,3-c]pyridine-2-carboxylic acid,1-[2-[(1-carboxy-3-phenylpropyl)amino]-1-oxopropyl]octahydro-6-[[[(phenylmethoxy)carbonyl]amino]acetyl]-
  • 1h-Pyrrolo[2,3-c]pyridine-2-carboxylic acid,1-[2-[[1-(ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]octahydro-6-[(methylamino)carbonyl]-,phenylmethyl ester
  • N-(4-fluorobenzyl)-2-(3-(3-(3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-5-yl)azetidin-1-yl)acetamide oxalate
  • 2,1,3-Benzoxadiazole-4-sulfonamide,n-[4,5-dichloro-2-(1h-1,2,4-triazol-1-ylmethyl)phenyl]-
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