155-90-8

  • Product Name:2-Amino-4-methoxypyrimidine
  • Molecular Formula:C5H7N3O
  • Purity:99%
  • Molecular Weight:125.13
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Product Details;

CasNo: 155-90-8

Molecular Formula: C5H7N3O

factory and supplier 155-90-8 2-Amino-4-methoxypyrimidine in stock

  • Molecular Formula:C5H7N3O
  • Molecular Weight:125.13
  • Vapor Pressure:0.000506mmHg at 25°C 
  • Melting Point:119-120 °C 
  • Refractive Index:1.566 
  • Boiling Point:313.131 °C at 760 mmHg 
  • PKA:5?+-.0.10(Predicted) 
  • Flash Point:143.177 °C 
  • PSA:61.03000 
  • Density:1.225 g/cm3 
  • LogP:0.64860 

2-Pyrimidinamine, 4-methoxy- (9CI)(Cas 155-90-8) Usage

General Description

2-Pyrimidinamine, 4-methoxy- (9CI) is a chemical compound categorized under the pyrimidinamine class. It can also be referred to as 4-Methoxy-2-Pyrimidinamine. This organic compound is particularly known for its structural relationship to pyrimidine, a molecule with hydrogen, carbon, and nitrogen atoms which serves as a fundamental unit for many essential biological substances such as nucleic acids. The methoxy group in the molecule refers to a functional group consisting of a methyl group bound to an oxygen atom, enhancing its molecular properties. Despite the limited available literature, this compound may be applicable in scientific research settings, possibly in fields like molecular biology or organic chemistry. However, its exact uses and properties require further investigation.

InChI:InChI=1/C5H7N3O/c1-9-4-2-3-7-5(6)8-4/h2-3H,1H3,(H2,6,7,8)

155-90-8 Relevant articles

Highly efficient, chemoselective syntheses of 2-methoxy-4-substituted pyrimidines

Xu, Chunyan,Cheng, Chuanjie,Liu, Hongtao,Liu, Bo

, p. 545 - 548 (2011)

Three 2-methoxy-4-substituted pyrimidine...

Synthesis and biological evaluation of novel flexible nucleoside analogues that inhibit flavivirus replication in vitro

Thames, Joy E.,Waters, Charles D.,Valle, Coralie,Bassetto, Marcella,Aouadi, Wahiba,Martin, Baptiste,Selisko, Barbara,Falat, Arissa,Coutard, Bruno,Brancale, Andrea,Canard, Bruno,Decroly, Etienne,Seley-Radtke, Katherine L.

, (2020)

Flaviviruses, such as Dengue (DENV) and ...

Phototransformation of Chlorimuron-ethyl in Aqueous Solution

Choudhury, Partha P.,Dureja, Prem

, p. 3379 - 3382 (1996)

Chlorimuron-ethyl is relatively stable i...

-

Hilbert,Johnson

, p. 1152,1156; vgl. H 24 80 (1930)

-

C2-Selective, Functional-Group-Divergent Amination of Pyrimidines by Enthalpy-Controlled Nucleophilic Functionalization

Ham, Won Seok,Choi, Hoonchul,Zhang, Jianbo,Kim, Dongwook,Chang, Sukbok

supporting information, p. 2885 - 2892 (2022/02/23)

Synthesis of heteroaryl amines has been ...

2-MORPHOLIN-4,6-DISUBSTITUTED PYRIMIDINE DERIVATIVE, AND PREPARATION METHOD AND PHARMACEUTICAL USE THEREOF

-

Paragraph 0108, (2017/11/11)

Disclosed is a 2-morpholin-4,6-disubstit...

Peptide deformylase inhibitors

-

Page/Page column, (2014/12/09)

The present invention relates to a compo...

155-90-8 Process route

chlorimuron ethyl
90982-32-4

chlorimuron ethyl

4-methoxypyrimidin-2-amine
155-90-8

4-methoxypyrimidin-2-amine

2-amino-4-chloro-6-methoxypyrimidine
5734-64-5

2-amino-4-chloro-6-methoxypyrimidine

ethyl 2-(aminosulfonyl)benzoate
59777-72-9

ethyl 2-(aminosulfonyl)benzoate

saccharin
81-07-2

saccharin

N-(6-Chloro-4-methoxypyrimidin-2-yl)urea

N-(6-Chloro-4-methoxypyrimidin-2-yl)urea

chlorimuron
99283-00-8

chlorimuron

Conditions
Conditions Yield
With water; for 2h; Product distribution; Rate constant; Irradiation; var. pH values;
2-amino-4-chloro-6-methoxypyrimidine
5734-64-5

2-amino-4-chloro-6-methoxypyrimidine

4-methoxypyrimidin-2-amine
155-90-8

4-methoxypyrimidin-2-amine

Conditions
Conditions Yield
With hydrogen; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; In ethanol; ethyl acetate; for 14h;
94%
With hydrogen; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; In ethanol; ethyl acetate; for 14h;
90%
With hydrogen; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; In ethanol; ethyl acetate; for 14h;
90%
With palladium 10% on activated carbon; hydrogen; N-ethyl-N,N-diisopropylamine; In ethanol; ethyl acetate; for 14h;
90%
With palladium 10% on activated carbon; hydrogen; N-ethyl-N,N-diisopropylamine; In methanol; ethyl acetate; at 20 ℃; for 4h;
85%
With hydrogenchloride; zinc; at 40 ℃;
With potassium hydroxide; Lindlar's catalyst; Hydrogenation;

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