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4-Pyrimidinamine, 2-methyl- (9CI)

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Company Name: ATK CHEMICAL COMPANY LIMITED
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Products Intro: CAS:74-69-1
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
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Products Intro: Product Name:4-Pyrimidinamine, 2-methyl- (9CI)
CAS:74-69-1
Purity:0.99 Package:5KG;1KG
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Products Intro: Product Name:2-Methyl-4-pyrimidinamine
CAS:74-69-1
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-07387
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Products Intro: Product Name:4-Pyrimidinamine, 2-methyl- (9CI)
CAS:74-69-1
Purity:99% HPLC Package:5KG;1KG
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:2-methyl-4-pyrimidinamine
CAS:74-69-1
Purity:0.99 Package:1kg

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4-Pyrimidinamine, 2-methyl- (9CI) Basic information
Product Name:4-Pyrimidinamine, 2-methyl- (9CI)
Synonyms:4-Pyrimidinamine, 2-methyl- (9CI);2-methylpyrimidin-4-amine;4-Amino-2-methylpyrimidine;2-Methyl-4-pyrimidinamine;4-PyriMidinaMine,2-Methyl;2-Methylpyrimidin-4-amine 98%;184573;2-Methyl-4-Pyrimidinamine(WX606010)
CAS:74-69-1
MF:C5H7N3
MW:109.13
EINECS:205-525-8
Product Categories:PYRIMIDINE
Mol File:74-69-1.mol
4-Pyrimidinamine, 2-methyl- (9CI) Structure
4-Pyrimidinamine, 2-methyl- (9CI) Chemical Properties
Melting point 204-205℃
Boiling point 222℃
density 1.155
Fp 111℃
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka5.99±0.10(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C5H7N3/c1-4-7-3-2-5(6)8-4/h2-3H,1H3,(H2,6,7,8)
InChIKeyGKVDLTTVBNOGNJ-UHFFFAOYSA-N
SMILESC1(C)=NC=CC(N)=N1
Safety Information
Hazard Codes Xn
Risk Statements 22-37/38-41
Safety Statements 26-39
HS Code 2933599590
MSDS Information
4-Pyrimidinamine, 2-methyl- (9CI) Usage And Synthesis
Synthesis Reference(s)Tetrahedron Letters, 7, p. 4325, 1966 DOI: 10.1016/0005-2760(66)90119-6
Synthesis
Trimethyl orthoacetate

1445-45-0

3-Methoxyacrylonitrile

60838-50-8

4-Pyrimidinamine, 2-methyl- (9CI)

74-69-1

The general procedure for the synthesis of 2-methyl-4-aminopyrimidine from trimethyl orthoacetate and 3-methoxyacrylonitrile was as follows: in a 10 mL stainless steel pressure-resistant reactor, 1.0 g (12 mmol) of 3-methoxyacrylonitrile, 3.9 g (32 mmol) of trimethyl orthoacetate, and 4.0 g (56 mmol) of 24 wt% ammonia-methanol solution were added in sequence. The reaction mixture was stirred at 130°C for 8 hours. After completion of the reaction, 20 mL of hexane was added to the reaction mixture, stirred thoroughly and filtered to afford 0.94 g (isolated yield: 72%) of the target product 2-methyl-4-aminopyrimidine as yellow crystals. 2-methyl-4-aminopyrimidine was characterized physically as follows: 1H-NMR (DMSO-d6, δ/ppm): 2.29 (3H, s), 6.22 (1H, dd, J = 5.9), 4.0 g (56 mmol) of 24 wt% ammonia-methanol solution. dd, J = 5.9, 0.5 Hz), 6.69 (2H, brs), 7.94 (1H, d, J = 5.9 Hz); CI-MS (m/e): 109 (M + 1).

References[1] Patent: US2008/45712, 2008, A1. Location in patent: Page/Page column 3-4
Tag:4-Pyrimidinamine, 2-methyl- (9CI)(74-69-1) Related Product Information
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