ChemicalBook >> CAS DataBase List >>9,10-DIDEHYDRO-6-METHYL-ERGOLINE-8-CARBOXYLIC ACID

9,10-DIDEHYDRO-6-METHYL-ERGOLINE-8-CARBOXYLIC ACID

CAS No.
82-58-6
Chemical Name:
9,10-DIDEHYDRO-6-METHYL-ERGOLINE-8-CARBOXYLIC ACID
Synonyms
(6aR,9R)-7-methyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]quinoline-9-carboxylic acid;Lysergic;lysergicacid;Ergoline Acid;Lyserginezuur;D-Lysergic acid hydrate,95%;D-LYSERGIC ACID HYDRATE 95%;Ergometrine Maleate Impurity A;Ergometrine Maleate EP Impurity A;Methylergometrine Maleate Impurity A
CBNumber:
CB8261074
Molecular Formula:
C16H16N2O2
Molecular Weight:
268.31
MDL Number:
MFCD00133297
MOL File:
82-58-6.mol
Last updated:2023-05-04 17:41:45

9,10-DIDEHYDRO-6-METHYL-ERGOLINE-8-CARBOXYLIC ACID Properties

Melting point >170°C (dec.)
alpha D20 +40° (c = 0.5 in pyridine)
Boiling point 411.48°C (rough estimate)
Density 1.1028 (rough estimate)
vapor pressure 0Pa at 20℃
refractive index 1.6240 (estimate)
storage temp. Controlled Substance, -20°C Freezer
pka 3.44, 7.68(at 25℃)
Water Solubility 267mg/L at 20℃
LogP -0.7 at 20℃
FDA UNII ITO20DAO7J

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302+H332
HS Code  29396300
DEA Controlled Substances CSCN: 7300
CSA SCH: Schedule III
NARC: No

9,10-DIDEHYDRO-6-METHYL-ERGOLINE-8-CARBOXYLIC ACID Chemical Properties,Uses,Production

Description

A precursor of the semisynthetic ergot derivatives, but having no biological activity itself. It is subject to controls under the Controlled Substances Act of 1970 in the United States, since it is the immediate precursor for the synthesis of LSD. Lysergic acid is obtained by hydrolysis of ergot alkaloids, either obtained from grains infected with Claviceps or, more commonly, by fermentation in submerged culture.

Chemical Properties

beige to brown powder

Uses

Labelled Lysergic acid. Lysergic acid and iso-lysergic acid are the main cleavage products formed on alkaline hydrolysis of the alkaloids which are characteristic of ergot. Potent hallucinogen; non-selective serotonin receptor agonist. Controlled substanc

Uses

Lysergic acid and iso-lysergic acid are the main cleavage products formed on alkaline hydrolysis of the alkaloids which are characteristic of ergot. Potent hallucinogen; non-selective serotonin receptor agonist. Controlled substance.

Definition

ChEBI: An ergoline alkaloid comprising 6-methylergoline having additional unsaturation at the 9,10-position and a carboxy group at the 8-position.

Synthesis Reference(s)

Journal of the American Chemical Society, 78, p. 3087, 1956 DOI: 10.1021/ja01594a039

Flammability and Explosibility

Not classified

Purification Methods

It crystallises from water as a hydrate. The methyl ester crystallises from C6H6 and has m 168o; the amide [478-94-4] has m 242o(dec) (from MeOH) and []546 +15o (c 0.5, pyridine).The (-)-hydrochloride has m 208-210o(dec, from MeOH). [Kornfeld et al. J Am Chem Soc 7 6 5256 1954,Kornfeld et al. J Am Chem Soc 78 3087 1956, Beilstein 25 III/IV 934,]

1159774-79-4
82-58-6
Synthesis of 9,10-DIDEHYDRO-6-METHYL-ERGOLINE-8-CARBOXYLIC ACID from Ergoline-8-carboxylic acid, 9,10-didehydro-6-methyl-, methyl ester
lysergicacid 9,10-DIDEHYDRO-6-METHYL-ERGOLINE-8-CARBOXYLIC ACID D-LYSERGIC ACID HYDRATE 95% LYSERGIC ACID(9,10-DIDEHYDRO-6-METHYLERGOLINE-8-CARBOXYLIC ACID) 9,10-Didehydro-6-methylergoline-8-carboxylic Quinapril hydrochloride,(3S)-2-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid hydrochloride D-Lysergic acid hydrate,95% (6aR,9R)-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxylic acid Lyserginezuur Ergoline-8-carboxylicacid, 9,10-didehydro-6-methyl-, (8b)- Ergoline Acid Ergoline-8-carboxylic acid, 9,10-didehydro-6-methyl-, (8β)- Lysergic (6aR,9R)-7-methyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]quinoline-9-carboxylic acid Ergometrine Maleate Impurity A Methylergometrine Maleate Impurity A Ergometrine Maleate EP Impurity A Methylergometrine Maleate EP Impurity A 82-58-6 C16H16N2O2xH2O C16H13D3N2O2 Chiral Reagents Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Isotope Labelled Compounds