Ro 16-6491

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Names

[ CAS No. ]:
94319-79-6

[ Name ]:
Ro 16-6491

[Synonym ]:
Ro 16-6491 hydrochloride
Ro 16-6491

Chemical & Physical Properties

[ Boiling Point ]:
404.2ºC at 760 mmHg

[ Melting Point ]:
209-210ºC

[ Molecular Formula ]:
C9H12Cl2N2O

[ Molecular Weight ]:
235.11000

[ Flash Point ]:
198.2ºC

[ Exact Mass ]:
234.03300

[ PSA ]:
55.12000

[ LogP ]:
2.92170

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924299090

Customs

[ HS Code ]: 2924299090

[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

The effects of phenelzine and other monoamine oxidase inhibitor antidepressants on brain and liver I2 imidazoline-preferring receptors.

Br. J. Pharmacol. 114(4) , 837-45, (1995)

1. The binding of [3H]-idazoxan in the presence of 10(-6) M (-)-adrenaline was used to quantitate I2 imidazoline-preferring receptors in the rat brain and liver after chronic treatment with various ir...

Overview of the present state of MAO inhibitors.

J. Neural Transm. Suppl. 23 , 103-19, (1987)

In this paper an overview of the present state of monoamine oxidase inhibitors (MAOIs) is presented. The irreversible inhibitors are firstly considered. They have been divided into four chemical types...

Synthesis and characterization of [125I]N-(2-aminoethyl)-4-iodobenzamide as a selective monoamine oxidase B inhibitor.

Nucl. Med. Biol. 22(5) , 617-23, (1995)

We described the radiosynthesis of an analog of Ro 16-6491, [125I]N-(2-aminoethyl)-4-iodobenzamide, for SPECT exploration of the monoamine oxidase B (MAO-B) in human brain. The radiolabelling was carr...


More Articles


Related Compounds

  • Ro 16-6127
  • Bretazenil
  • Lodazecar
  • 4-chloro-N-[2-(2-hydroxyethylamino)ethyl]benzamide
  • 4-(3-(bis(beta-hydroxyphenethyl)amino)butyl)benzamide
  • (Z)-7-[(1R,2R,3R)-2-[(E,3R)-3-acetyloxy-4,4-dimethyloct-1-enyl]-3-methyl-5-oxocyclopentyl]hept-5-enoic acid
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 3-Tert-butyl-1-oxa-3,7-diazaspiro[4.5]decan-2-one
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • 6-(4-(Methylsulfonyl)piperazin-1-yl)picolinaldehyde
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine