CAS 83774-09-8

2-Chloro-4-ethoxypyrimidine

Description:

2-Chloro-4-ethoxypyrimidine is a heterocyclic organic compound characterized by a pyrimidine ring substituted with a chlorine atom and an ethoxy group. Its molecular structure features a six-membered ring containing two nitrogen atoms at positions 1 and 3, which is typical of pyrimidines. The presence of the chlorine atom at the 2-position and the ethoxy group at the 4-position contributes to its unique chemical reactivity and properties. This compound is typically a colorless to pale yellow liquid or solid, depending on its form and purity. It is soluble in organic solvents and may exhibit moderate stability under standard conditions. 2-Chloro-4-ethoxypyrimidine is of interest in medicinal chemistry and agricultural applications, often serving as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactivity can be attributed to the electrophilic nature of the chlorine atom, making it a potential candidate for further chemical modifications. Safety data should be consulted for handling and storage, as it may pose health risks if not managed properly.

Formula: C₆H₇ClN₂O

2-Chloro-4-ethoxy-pyrimidine

CAS: 83774-09-8

Formula: C₆H₇ClN₂O

Purity: 98%

Color and Shape: Solid

Molecular weight: 158.5856

Ref: IN-DA0036EK

2-Chloro-4-ethoxy-pyrimidine

CAS: 83774-09-8

2-Chloro-4-ethoxy-pyrimidine

Purity: 95%

Molecular weight: 158.59g/mol

Ref: 54-OR350087

2-Chloro-4-ethoxy-pyrimidine

CAS: 83774-09-8

Formula: C₆H₇ClN₂O

Purity: 95%

Color and Shape: Crystalline

Molecular weight: 158.59

Ref: 10-F088413

2-Chloro-4-ethoxypyrimidine

CAS: 83774-09-8

2-Chloro-4-ethoxypyrimidine is a transition metal compound with a high reactivity. It has been shown to undergo an elimination reaction with chloro substituents and nitrogen in the presence of electron acceptors such as oxygen, water, or peroxides. The kinetic rate is statistically dependent on the size of the substituents and the substituent's position on the ring. Substituents that are coplanar with the reactive site have a higher rate of substitution than those that are not coplanar.

Formula: C₆H₇ClN₂O

Purity: Min. 95%

Molecular weight: 158.59 g/mol

Ref: 3D-IDA77409