CAS 14160-93-1

4-Amino-6-chloropyrimidine-5-carbaldehyde

Description:

4-Amino-6-chloropyrimidine-5-carbaldehyde is a heterocyclic organic compound characterized by its pyrimidine ring structure, which includes an amino group and a chlorinated position. The presence of the aldehyde functional group at the 5-position contributes to its reactivity, making it useful in various chemical syntheses. This compound typically appears as a solid and is soluble in polar solvents, reflecting its functional groups' ability to engage in hydrogen bonding. It is often utilized in pharmaceutical chemistry and the synthesis of biologically active molecules due to its potential as an intermediate in the development of drugs. The compound's reactivity can be attributed to the electron-withdrawing effects of the chlorine atom and the aldehyde group, which can influence its behavior in nucleophilic reactions. Safety data indicates that, like many nitrogen-containing heterocycles, it should be handled with care, as it may pose health risks if ingested or inhaled. Overall, 4-Amino-6-chloropyrimidine-5-carbaldehyde is a valuable compound in organic synthesis and medicinal chemistry.

Formula: C₅H₄ClN₃O

InChI: InChI=1/C5H4ClN3O/c6-4-3(1-10)5(7)9-2-8-4/h1-2H,(H2,7,8,9)

InChI key: InChIKey=GOJNFUXEBVBARW-UHFFFAOYSA-N

SMILES: C(=O)C=1C(Cl)=NC=NC1N

Synonyms:

• 4-Amino-6-chloro-5-pyrimidine carbaldehyde
• 4-Amino-6-chloro-5-pyrimidinecarboxaldehyde
• 4-Amino-6-chloro-pyrimidine-5-carbaldehyde
• 4-Amino-6-chloropyrimidine-5-carboxaldehyde
• 5-Pyrimidinecarboxaldehyde, 4-amino-6-chloro-
• 6-Chloro-5-difluoromethyl-pyrimidin-4-ylamine
• 4-Amino-6-chloropyrimidine-5-carbaldehyde
• 4-Chloro-6-aminopyrimidine-5-carbaldehyde
• 4-Amino-6-chloro-5-formylpyrimidine, 4-Amino-6-chloro-5-formyl-1,3-diazine
• 4-Amino-6-chloropyrimidine-5-carboxaldehyde,97%
• 5-PyriMidinecarbaldehyde, 4-aMino-6-chloro
• RARECHEM AK ML 0569
• 4-Amino-6-chloro-5-pyrimidinecarboxaldehyde ,96%
• 4-AMINO-6-CHLORO-PYRIMIDINE-5-CARBALDEHYDE ISO 9001：2015 REACH
• 4-AMINO-6-CHLORO-5-PYRIMIDINECARBALDEHYDE
• 4-aMino-6-chloro-pyriMidine-5-carbaledhyde

4-Amino-6-chloropyrimidine-5-carboxaldehyde

CAS: 14160-93-1

4-Amino-6-chloropyrimidine-5-carboxaldehyde

Formula: C₅H₄ClN₃O

Purity: ≥95%

Color and Shape: Solid

Molecular weight: 157.55775

Ref: 54-OR6659

4-Amino-6-chloro-5-pyrimidinecarboxaldehyde

CAS: 14160-93-1

Formula: C₅H₄ClN₃O

Purity: 98%

Color and Shape: Solid

Molecular weight: 157.5578

Ref: IN-DA001GOE

4-Amino-6-chloropyrimidine-5-carbaldehyde

CAS: 14160-93-1

4-Amino-6-chloropyrimidine-5-carbaldehyde

Formula: C₅H₄ClN₃O

Purity: 95%

Molecular weight: 157.56

Ref: IN-DG27510

4-Amino-6-chloro-pyrimidine-5-carbaldehyde

CAS: 14160-93-1

Formula: C₅H₄ClN₃O

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 157.56

Ref: 10-F080063

4-Amino-6-chloropyrimidine-5-carbaldehyde

CAS: 14160-93-1

4-Amino-6-chloropyrimidine-5-carbaldehyde is a reactive molecule that is used in the synthesis of macrocyclic aldehydes. It is prepared by the oxidation of anilines with oxalyl chloride in the presence of hydrochloric acid and amines. 4-Amino-6-chloropyrimidine-5-carbaldehyde reacts with hydrazine to form diamines, which are used as building blocks for pharmaceuticals. This molecule has been shown to have anticancer properties, by inhibiting DNA replication and cell growth through its ability to inhibit protein synthesis.

Formula: C₅H₄ClN₃O

Purity: Min. 95%

Molecular weight: 157.56 g/mol

Ref: 3D-NA57367