ChemicalBook--->CAS DataBase List--->42754-96-1

42754-96-1

42754-96-1 Structure

42754-96-1 Structure
IdentificationBack Directory
[Name]

4,6-DICHLORO-1H-PYRAZOLO[3,4-D]PYRIMIDINE
[CAS]

42754-96-1
[Synonyms]

SKL327
6-Dichloro-1H-pyrazolo[3
4,6-dichloropyrrolo[2,3-d]pyrimidine
4,6-Dichloropyrazolo[3,4-d]pyriMidine
4,6-dichloro-1H-pyrazolo[3,4-d]pP03119ine
4,6-Dichloro-1H-pyrazole[3,4-D]pyriMidine
4,6-DICHLORO-1H-PYRAZOLO[3,4-D]PYRIMIDINE
4,6-dichloro-2H-pyrazolo[3,4-d]pyrimidine
1H-Pyrazolo[3,4-d]pyrimidine,4,6-dichloro-
4,6-DICHLORO-1H-PYRAZOLO[3,4-D]PYRIMIDINE(RS20012005)
[EINECS(EC#)]

948-193-9
[Molecular Formula]

C5H2Cl2N4
[MDL Number]

MFCD09835493
[MOL File]

42754-96-1.mol
[Molecular Weight]

189
Chemical PropertiesBack Directory
[Melting point ]

145 °C (decomp)
[Boiling point ]

251.9±50.0 °C(Predicted)
[density ]

2.02±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

solid
[pka]

7.90±0.20(Predicted)
[color ]

Off-white to yellow
[InChI]

InChI=1S/C5H2Cl2N4/c6-3-2-1-8-11-4(2)10-5(7)9-3/h1H,(H,8,9,10,11)
[InChIKey]

CTYPROOLWJDUTA-UHFFFAOYSA-N
[SMILES]

C1(Cl)=NC(Cl)=C2C=NNC2=N1
Questions And AnswerBack Directory
[Uses]

4,6-Dichloro-1H-pyrazolo[3,4-C]pyrimidine is a heterocyclic organic compound that can be used as a pharmaceutical intermediate.
[Application]

4,6-Dichloro-1H-pyrazolo[3,4-C]pyrimidine is an organic synthesis intermediate and a pharmaceutical intermediate, mainly used in laboratory research and development processes and chemical production processes.
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45-24/25
[RIDADR ]

UN2811
[HazardClass ]

IRRITANT
[HS Code ]

29335990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

2,4,6-Trichloro-pyrimidine-5-carbaldehyde-->Oxipurinol
Hazard InformationBack Directory
[Chemical Properties]

Yellow solid
[Synthesis]

To a solution of 2,4,6-trichloropyrimidine-5-carbaldehyde (19.0 g, 990 mmol) in methanol (300 mL) was added drop-wise a solution of hydrazine monohydrate (4.8 mL) in methanol (80 mL) at 0 °C followed by drop-wise addition of triethylamine (13 mL) in methanol (80 mL) at 0 °C. The mixture was stirred at the same temperature for 30 mm. The solvent was removed, and the residue was purified by flash chromatography to afford 4,6-Dichloro-1H-pyrazolo[3,4-d]pyrimidine (10.3 g, 62 % yield) as a yellow solid. ‘H NMR (CDC13, 400IVIHz): 11.56 (br, 1H), 8.43 (s, 1H). MS m/z 190.68 [M+1].
[References]

[1] Patent: EP1772454, 2007, A1. Location in patent: Page/Page column 58
[2] Patent: WO2010/56320, 2010, A2. Location in patent: Page/Page column 60
[3] ACS Medicinal Chemistry Letters, 2015, vol. 6, # 5, p. 584 - 589
[4] Patent: WO2016/130920, 2016, A2. Location in patent: Page/Page column 119
[5] Patent: , 2016, . Location in patent: Paragraph 0019
Spectrum DetailBack Directory
[Spectrum Detail]

4,6-DICHLORO-1H-PYRAZOLO[3,4-D]PYRIMIDINE(42754-96-1)1HNMR
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