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2-Chloro-5-hydroxypyrimidine

2-Chloro-5-hydroxypyrimidine Suppliers list
Company Name: Shandong Shining Pharm Co.,Ltd  Gold
Tel: 18866891188 18866891188
Email: zhaojiangxia@shiningpharm.com
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Tel: 4000255188
Email: marketing@pharmablock.com
Company Name: Haimen Ruiyi Medical Tech Co., LTD  Gold
Tel: 021-54718086
Email: sales5@ruiyitech.com
Company Name: Hangzhou Copiore Chemical Co., Ltd.  Gold
Tel: 17300981287 13757145729
Email: sales@copiore.com
Company Name: Beijing Huize Zhongsen Pharmaceutical Technology Co., Ltd.  Gold
Tel: 18519331287 18519331287
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2-Chloro-5-hydroxypyrimidine manufacturers

2-Chloro-5-hydroxypyrimidine Basic information
Product Name:2-Chloro-5-hydroxypyrimidine
Synonyms:2-Chloro-5-hydroxypyrimidine 98%;2-Chloro-5-hydroxypyrimidine;5-Pyrimidinol, 2-chloro- (7CI,8CI,9CI);2-Chloro-5-hydroxypyrimid...;5-PyriMidinol,2-chloro-;2-Chloropyrimidin-5-ol, 2-Chloro-5-hydroxy-1,3-diazine;2-Chloro-5-pyrimidinol;2-Chloro-5-hydroxypyrimidine ISO 9001:2015 REACH
CAS:4983-28-2
MF:C4H3ClN2O
MW:130.53
EINECS:826-504-8
Product Categories:Heterocycle-Pyrimidine series;PYRIMIDINE;pharmacetical;Pyrimidines
Mol File:4983-28-2.mol
2-Chloro-5-hydroxypyrimidine Structure
2-Chloro-5-hydroxypyrimidine Chemical Properties
Melting point 195-196 °C
Boiling point 328.1±15.0 °C(Predicted)
density 1.513±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka6.17±0.23(Predicted)
AppearanceOff-white to light brown Solid
InChIInChI=1S/C4H3ClN2O/c5-4-6-1-3(8)2-7-4/h1-2,8H
InChIKeyBOGPIHXNWPTGNH-UHFFFAOYSA-N
SMILESC1(Cl)=NC=C(O)C=N1
CAS DataBase Reference4983-28-2(CAS DataBase Reference)
Safety Information
HS Code 29335990
MSDS Information
2-Chloro-5-hydroxypyrimidine Usage And Synthesis
Uses2-Chloro-5-hydroxypyrimidine is an intermediate used to synthesize tandospirone derivatives with anxiolytic activities.
Hazard2-Chloro-5-hydroxypyrimidine is an irritant. Contact may cause skin irritation, severe eye irritation and respiratory tract irritation.
Synthesis2-Chloro-5-methoxypyrimidine (0.46 g, 3.18 mmol) in methylene chloride (10 mL) was treated with 1.0 N boron tribromide (16 mL, 16 mmol) at room temperature. The solution was stirred overnight. After that, the reaction was partitioned between saturated NaHCO3 and DCM. The aqueous layer was extracted with additional DCM. Combined the organic layers and dried (MgSO4), filtered, and concentrated to obtain the crude product. The residue was purified by flash column chromatography on silica gel to give 2-Chloro-5-hydroxypyrimidine.2-Chloro-5-hydroxypyrimidine

References[1] Patent: WO2010/80503, 2010, A1. Location in patent: Page/Page column 225
[2] Patent: WO2011/144578, 2011, A1. Location in patent: Page/Page column 27
[3] Patent: WO2011/144577, 2011, A1. Location in patent: Page/Page column 24-25
[4] Patent: WO2016/164703, 2016, A1. Location in patent: Page/Page column 50
[5] Patent: US5589478, 1996, A
2-Chloro-5-hydroxypyrimidine Preparation Products And Raw materials
Raw materials2-Chloro-5-methoxypyrimidine-->Dichloromethane-->5-Amino-2-chloropyrimidine-->Boron tribromide
Tag:2-Chloro-5-hydroxypyrimidine(4983-28-2) Related Product Information
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