CAS 16357-83-8

5-Pyrimidinecarboxaldehyde, 4-amino- (8CI,9CI)

Description:

5-Pyrimidinecarboxaldehyde, 4-amino- is an organic compound characterized by a pyrimidine ring, which is a six-membered heterocyclic structure containing two nitrogen atoms at positions 1 and 3. This compound features an aldehyde functional group (-CHO) at the 5-position and an amino group (-NH2) at the 4-position of the pyrimidine ring. Its molecular structure contributes to its reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of both the amino and aldehyde groups allows for diverse chemical reactions, such as condensation and substitution reactions, making it a valuable intermediate in organic synthesis. Additionally, this compound may exhibit biological activity, which can be explored for potential therapeutic uses. As with many nitrogen-containing heterocycles, it may also participate in hydrogen bonding, influencing its solubility and interaction with other molecules. Safety and handling precautions should be observed, as with any chemical substance, due to potential toxicity or reactivity.

Formula: C₅H₅N₃O

InChI: InChI=1/C5H5N3O/c6-5-4(2-9)1-7-3-8-5/h1-3H,(H2,6,7,8)

SMILES: c1c(C=O)c(=N)[nH]cn1

Synonyms:

• 4-Aminopyrimidine-5-carbaldehyde

5-Pyrimidinecarboxaldehyde, 4-amino-

CAS: 16357-83-8

Formula: C₅H₅N₃O

Purity: 97%

Color and Shape: Solid

Molecular weight: 123.1127

Ref: IN-DA001U8M

4-Aminopyrimidine-5-Carbaldehyde

CAS: 16357-83-8

4-Aminopyrimidine-5-Carbaldehyde

Purity: 95%

Molecular weight: 123.11g/mol

Ref: 54-OR1027318

4-Aminopyrimidine-5-carbaldehyde

CAS: 16357-83-8

Formula: C₅H₅N₃O

Purity: 97%

Molecular weight: 123.115

Ref: 10-F233877

4-Aminopyrimidine-5-carboxaldehyde

CAS: 16357-83-8

4-Aminopyrimidine-5-carboxaldehyde is a molecule that has been found to cause regression of cancer. It targets the erbb-2 receptor, which is necessary for cell growth and survival in many types of cancer. This compound has been shown to inhibit the growth of cancer cells in vitro by downregulating the expression of erbb-2. The molecular descriptors have been calculated using an algorithm and are used to describe the physical properties of this molecule. It has been shown that it is effective at inhibiting tumor growth and inducing regression in mice bearing human breast tumors xenografted with human breast cancer cells. 4-Aminopyrimidine-5-carboxaldehyde has also been shown to inhibit colorectal cancer cell proliferation by reducing cellular protein synthesis.
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This molecule's structure consists of a 4-amino group, a pyrimidine ring, and an aldehyde group. It contains functional groups such as carb

Formula: C₅H₅N₃O

Purity: Min. 95%

Molecular weight: 123.11 g/mol

Ref: 3D-RAA35783