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63001-30-9

63001-30-9 Structure

63001-30-9 Structure
IdentificationBack Directory
[Name]

METHYL 6-OXO-1,6-DIHYDROPYRIDAZINE-3-CARBOXYLATE
[CAS]

63001-30-9
[Synonyms]

AKOS BBS-00006829
Methyl 3-hydroxypyridazin...
Methyl 6-oxopyridazine-3-carboxylate
methyl 6-oxo-1H-pyridazine-3-carboxylate
Methyl 3-hydroxypyridazine-6-carboxylate
methyl 6-hydroxypyridazine-3-carboxylate
1,6-Dihydro-3-(methoxycarbonyl)-6-oxopyridazine
Methyl 1,6-dihydro-6-oxopyridazine-3-carboxylate
METHYL 6-OXO-1,6-DIHYDROPYRIDAZINE-3-CARBOXYLATE
6-oxo-1H-pyridazine-3-carboxylic acid methyl ester
Methyl 1,6-dihydro-6-oxopyridazine-3-carboxylate 97%
1,6-dihydro-6-oxo-3-Pyridazinecarboxylic acid methyl ester
6-oxo-1,6-dihydro-pyridazine-3-carboxylic acid Methyl ester
3-Pyridazinecarboxylic acid, 1,6-dihydro-6-oxo-, methyl ester
METHYL 6-OXO-1,6-DIHYDROPYRIDAZINE-3-CARBOXYLATE ISO 9001:2015 REACH
1,6-Dihydro-3-(methoxycarbonyl)-6-oxopyridazine, 1,6-Dihydro-3-(methoxycarbonyl)-6-oxo-1,2-diazine
[Molecular Formula]

C6H6N2O3
[MDL Number]

MFCD08166726
[MOL File]

63001-30-9.mol
[Molecular Weight]

154.12
Chemical PropertiesBack Directory
[Melting point ]

188 °C
[density ]

1.39±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

10.34±0.40(Predicted)
[Appearance]

Off-white to light brown Solid
[InChI]

InChI=1S/C6H6N2O3/c1-11-6(10)4-2-3-5(9)8-7-4/h2-3H,1H3,(H,8,9)
[InChIKey]

REYKVZJYIFOXTI-UHFFFAOYSA-N
[SMILES]

C1(C(OC)=O)=NNC(=O)C=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

METHYL 6-OXO-1,6-DIHYDROPYRIDAZINE-3-CARBOXYLATE(63001-30-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

6-Oxo-1,6-dihydro-pyridazine-3-carboxylicacid

37972-69-3

METHYL 6-OXO-1,6-DIHYDROPYRIDAZINE-3-CARBOXYLATE

63001-30-9

A. 6-Hydroxypyridazine-3-carboxylic acid (5.00 g, 31.6 mmol) was dissolved in methanol and thionyl chloride (0.36 mL, 0.59 g, 4.94 mmol) was added slowly. The reaction mixture was heated to reflux at 80 °C for 16 hours. After completion of the reaction, it was cooled to room temperature and the product crystallized. The crystals were collected by filtration and washed with cold methanol. The mother liquor was combined, concentrated and crystallized again to give methyl 6-oxo-1,6-dihydropyridazine-3-carboxylate in a total yield of 4.954 g (100% yield).

[References]

[1] Patent: WO2006/34440, 2006, A2. Location in patent: Page/Page column 43
[2] Patent: US2011/257173, 2011, A1. Location in patent: Page/Page column 19; 21
[3] Patent: US2011/105509, 2011, A1. Location in patent: Page/Page column 30; 31; 32
[4] Patent: US2016/376283, 2016, A1. Location in patent: Paragraph 1225; 1227
[5] Patent: WO2004/89939, 2004, A1. Location in patent: Page 40-41
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