CAS No 478-84-2 , Ergoline-8-carboxamide,2-bromo-9,10-didehydro-N,N-diethyl-6-methyl-, (8b)-

Name: Ergoline-8-carboxamide,2-bromo-9,10-didehydro-N,N-diethyl-6-methyl-, (8b)-
Synonyms: 2-Bromo-LSD; 2-Bromolysergic acid diethylamide; D-2-Bromolysergic acid diethylamide; Bromolysergic acid diethylamide;Ergoline-8b-carboxamide,2-bromo-9,10-didehydro-N,N-diethyl-6-methyl- (8CI); 2-Bromolysergicdiethylamide; BOL 148; d-Bromolysergic aciddiethylamide; Indolo[4,3-fg]quinoline, ergoline-8-carboxamidederiv.; Bromo-LSD;Bromolysergide; 2-Bromo-d-lysergicacid diethylamide;Ergoline-8-carboxamide,2-bromo-9,10-didehydro-N,N-diethyl-6-methyl-, (8b)-; 2-Bromo-D-lysergic acid diethylamide; Lysergamide,2-bromo-N,N-diethyl- (5CI);
CAS Registry Number:478-84-2
Flash Point: 305°C
Boiling Point: 580.7°Cat760mmHg
Density: 1.44g/cm³
Refractive index: 1.676
Safety Statements: Poison by intraperitoneal and intravenous routes. Experimental teratogenic and reproductive effects. Human systemic effects by ingestion: dilation of the arteries or veins. Many lysergic acid derivatives have central nervous system effects. When heated to decomposition it emits very toxic fumes such as Br⁻ and NO_x. See other lysergic acid derivatives.
Flash Point: 305°C
Molecular Weight: 404.40
InChI: InChI=1/C20H24BrN3O/c1-4-24(5-2)20(25)12-9-14-13-7-6-8-16-18(13)15(19(21)22-16)10-17(14)23(3)11-12/h6-9,12,17,22H,4-5,10-11H2,1-3H3/t12-,17-/m1/s1
Molecular Formula: C20H24 Br N3 O
Molecular Structure:

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References of Ergoline-8-carboxamide,2-bromo-9,10-didehydro-N,N-diethyl-6-methyl-, (8b)-

Title: Bromolysergide
CAS Registry Number: 478-84-2
CAS Name: (8b)-2-Bromo-9,10-didehydro-N,N-diethyl-6-methylergoline-8-carboxamide
Synonyms: D-2-bromolysergic acid diethylamide; 2-bromo-N,N-diethyl-D-lysergamide; bromo-LSD
Manufacturers' Codes: BOL-148
Molecular Formula: C20H24BrN3O
Molecular Weight: 402.33
Percent Composition: C 59.71%, H 6.01%, Br 19.86%, N 10.44%, O 3.98%
Literature References: Prepd by bromination of lysergide, q.v.: Troxler, Hofmann, Helv. Chim. Acta 40, 2160 (1957). Serotonin antagonist without the hallucinogenic activity of LSD: J. P. Bennett, S. H. Snyder, Brain Res. 94, 523 (1975).
Properties: Needles from ether, mp 120-127°. [a]D20 +15° (c = 0.5 in pyridine); [a]D20 +53° (c = 0.5 in chloroform). uv max: 240, 301 nm (log e 4.28, 3.95).
Melting point: mp 120-127°
Optical Rotation: [a]D20 +15° (c = 0.5 in pyridine); [a]D20 +53° (c = 0.5 in chloroform)
Absorption maximum: uv max: 240, 301 nm (log e 4.28, 3.95)