Category: 876-21-1

The important role of (4-Amino-2-ethylpyrimidin-5-yl)methanol

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 876-21-1, (4-Amino-2-ethylpyrimidin-5-yl)methanol.

Application of 876-21-1, The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 876-21-1, name is (4-Amino-2-ethylpyrimidin-5-yl)methanol. This compound has unique chemical properties. The synthetic route is as follows.

4.59 g (0.03 mol) of 4-amino-2-ethyl-5-(hydroxymethyl)-pyrimidine was charged into a 100 ml flask, followed by 20 ml of dichloromethane, 20 ml of toluene and 0.1 ml of pyridine. 6.5 ml of thionyl chloride (0.28 mol) was dropped in slowly with cooling by ice bath. Then the reaction was stirred overnight. Solvent was removed and the residue was used for next step directly. 1H-NMR(400M, d-DMSO): 8.45 (s, 1H),4.80(s, 2H), 3.64(s, 2H), 2.80(dd, 2H, J=7.6,14.8), 1.24(t, 3H, J=7.6).

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 876-21-1, (4-Amino-2-ethylpyrimidin-5-yl)methanol.

Reference:
Patent; GUANGZHOU ORIGMOL FEED-ADDITIVE CO., LTD; Peng, Xianfeng; Qin, Zonghua; Liu, Qijun; US2015/133480; (2015); A1;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Some scientific research about (4-Amino-2-ethylpyrimidin-5-yl)methanol

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,876-21-1, its application will become more common.

Related Products of 876-21-1, In the chemical reaction process,reaction time,type of solvent,can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product.An updated downstream synthesis route of 876-21-1 as follows.

(3) Synthesis of 4-amino-5-chloromethyl-2-ethylpyrimidine hydrochloride 4.59 g (0.03 mol) of 4-amino-2-ethyl-5-(hydroxymethyl)-pyrimidine was charged into a 100 ml flask, followed by 20 ml of dichloromethane, 20 ml of toluene and 0.1 ml of pyridine. 6.5 ml of thionyl chloride (0.28 mol) was dropped in slowly with cooling by ice bath. Then the reaction was stirred overnight. Solvent was removed and the residue was used for next step directly. 1H-NMR (400M, d-DMSO): 8.45 (s, 1H), 4.80 (s, 2H), 3.64 (s, 2H), 2.80 (dd, 2H, J=7.6, 14.8), 1.24 (t, 3H, J=7.6).

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,876-21-1, its application will become more common.

Reference:
Patent; GUANGZHOU ORIGMOL FEED-ADDITIVE CO., LTD; Peng, Xianfeng; Qin, Zonghua; Liu, Qijun; US9096581; (2015); B2;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia