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132712-71-1

132712-71-1 Structure

132712-71-1 Structure
IdentificationBack Directory
[Name]

3-methyl-1H-pyrazol-5-ol
[CAS]

132712-71-1
[Synonyms]

3-methyl-1H-pyrazol-5-ol
5-Methyl-2H-pyrazol-3-ol
1H-Pyrazol-5-ol, 3-Methyl-
[Molecular Formula]

C4H6N2O
[MDL Number]

MFCD00462188
[MOL File]

132712-71-1.mol
[Molecular Weight]

98.1
Chemical PropertiesBack Directory
[Boiling point ]

309.7±22.0 °C(Predicted)
[density ]

1.296±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[pka]

3.51±0.23(Predicted)
[Appearance]

Off-white to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

3-methyl-1H-pyrazol-5-ol(132712-71-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

ETHYL 4-(4-METHOXYPHENYL)-6-METHYL-2-OXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBOXYLATE

161374-07-8

Benzaldehyde, 4-methoxy-, hydrazone

5953-85-5

Carbamimidothioic acid

17356-08-0

Urea

57-13-6

3-methyl-1H-pyrazol-5-ol

132712-71-1

The general procedure for the synthesis of compound (CAS:5953-85-5), compound (CAS:17356-08-0), urea and 3-methyl-1H-pyrazol-5-ol from compound (CAS:161374-07-8) was as follows: a-h of DHH (0.01 mol) was mixed with excess hydrazine hydrate (5 mL) and heated to reflux for 6 hr. . After completion of the reaction, the mixture was cooled and poured into crushed ice. The solid products a-d were collected by filtration, crystallized with ethanol and finally dried. Evaporation of the filtrate gave a solid residue, which was isolated by graded crystallization from water to obtain pyrazole and urea (a) or thiourea (b). 2.4.1. Synthesis of 3-methyl-1H-pyrazol-5-ol (13). Yield: 42-55% (based on a-h); Melting point: 221-223 °C (literature value [49]: 220-222 °C); 1H-NMR (DMSO-d6) δ (ppm): 2.47 (s, 3H, -CH3), 6.83 (s, 1H, Ar-H), 10.07 (s, 1H, OH), 12.10 (s, 1H, NH) .

[References]

[1] Journal of Chemistry, 2018, vol. 2018,
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