
4,5,6-Trichloropyrimidine | CAS:1780-27-4
4,5,6-Trichloropyrimidine
- Name:4,5,6-Trichloropyrimidine
- CAS:1780-27-4
- Synonyms:
- Molecular Formula:C4HCl3N2
- Molecular Weight:183.42
- EINESC:
Description
Properties
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Safety
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SDS
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Synthetic Route
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More
Articles
Peer-Reviewed Papers
Metabolism of allylglycine and cis-crotylglycine by Pseudomonas putida (arvilla) mt-2 harboring a TOL plasmid.D A Kunz et al.Journal of bacteriology, 148(1), 72-82 (1981-10-01)
Disruption of GABAergic tone in the dorsomedial hypothalamus attenuates responses in a subset of serotonergic neurons in the dorsal raphe nucleus following lactate-induced panic.Pl Johnson et al.Journal of psychopharmacology (Oxford, England), 22(6), 642-652 (2008-03-01)
Cyclic opioid peptide agonists and antagonists obtained via ring-closing metathesis.Irena Berezowska et al.Chemical biology & drug design, 74(4), 329-334 (2009-08-22)
Allylglycine and brain excitability. Electrophysiological investigation in cats.S Moyanova et al.Acta physiologica et pharmacologica Bulgarica, 15(1), 47-53 (1989-01-01)
Non-centrosymmetric racemates: space-group frequencies and conformational similarities between crystallographically independent molecules.Dalhus B, Gorbitz CH. Acta Physiologica Et Pharmacologica Bulgarica, 56, 715-719 (2000)
In vivo neurochemical evidence that newly synthesised GABA activates GABA(B), but not GABA(A), receptors on dopaminergic nerve endings in the nucleus accumbens of freely moving rats.Tadashi Saigusa et al.Neuropharmacology, 62(2), 907-913 (2011-10-04)
In vivo modulation of benzodiazepine receptor function after inhibition of endogenous gamma-aminobutyyric acid synthesis.M Bottlaender et al.European journal of pharmacology, 321(1), 13-17 (1997-02-19)
Remarks
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Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
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