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Home > Encyclopedia > 2-Hydroxy-4,6-dimethylpyrimidine

2-Hydroxy-4,6-dimethylpyrimidine

2-Hydroxy-4,6-dimethylpyrimidine structure

2-Hydroxy-4,6-dimethylpyrimidine 

structure
  • CAS No:

    108-79-2

  • Formula:

    C6H8N2O

  • Chemical Name:

    2-Hydroxy-4,6-dimethylpyrimidine

  • Synonyms:

    2(1H)-Pyrimidinone,4,6-dimethyl-;2-Pyrimidinol,4,6-dimethyl-;2(1H)-Pyrimidone,4,6-dimethyl-;4,6-Dimethyl-2(1H)-pyrimidinone;4,6-Dimethyl-2-pyrimidinol;2-Hydroxy-4,6-dimethylpyrimidine;4,6-Dimethyl-2-hydroxypyrimidine;4,6-Dimethyl-1,2-dihydro-2-pyrimidone;4,6-Dimethyl-2(1H)-pyrimidone;4,6-Dimethyl-2-pyrimidone;4,6-Dimethyl-1,2-dihydropyrimidin-2-one;3297-20-9

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

Description

Off-white, light yellow to pink crystalline powder

2-Hydroxy-4,6-dimethylpyrimidine Basic Attributes

124.14

124.14

203-617-5

HG0CBN4V9F

DTXSID5043762

29335990

Characteristics

41.5

0

1.29 g/cm3

197 °C

230.92°C (rough estimate)

144.0±28.7 °C

1.5378 (estimate)

Safety Information

IRRITANT

36/37/38

24/25-45-37-28

Xi

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 6 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

2-hydroxy-4,6-dimethylpyrimidine

2-Hydroxy-4,6-dimethylpyrimidine Use and Manufacturing

Methods of Manufacturing

IM06: 4, 6-Dimethyl-pyrimidin-5-ylamineStep 1:To a solution of urea (20.0 g, 333.3 mmol) and acetyl acetone (33.3 g, 333.3 mmol) in EtOH (166 mL) was added concentrated aqueous HCl (45 mL). The mixture was stirred at 80° C. for 24 h. The mixture was then cooled to room temperature, filtered and the remanens washed with cold EtOH to give 4, 6-dimethyl-pyrimidin-2-ol as a colorless solid (40 g, 97percent). 1H NMR (DMSO-d6, 400 MHz) δ 7.35 (1H, s), 2.43 (6H, s).To a solution of urea (20.0 g, 333.3 mmol) and acetyl acetone (33.3 g, 333.3 mmol) in EtOH (166 mL) was added concentrated aqueous HCI (45 mL). The mixture was stirred at 80 °C for 24h. The mixture was then cooled to room temperature, filtered and the remanens washed with cold EtOH to give 4, 6-dimethyl-pyrimidin-2-ol as a colorless solid (40 g, 97percent). 1 H NMR (DMSO-d6, 400 MHz) δ 7.35 (1 H, s), 2.43 (6H, s).

Uses

Mix with 4,4~"-dinitrodiphenylurea to obtain veterinary drug nicarbazin

2(1H)-Pyrimidinone, 4,6-dimethyl-: INACTIVE

Environmental transformation -> Pesticide transformation products (metabolite, successor)

2-hydroxy-4,6-dimethylpyrimidine is a known environmental transformation product of Pyrimethanil.

Computed Properties

Molecular Weight:124.14
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Exact Mass:124.063662883
Monoisotopic Mass:124.063662883
Topological Polar Surface Area:41.5
Heavy Atom Count:9
Complexity:203
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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