CAS 32968-44-8

acetaldehyde, 5-methyloxazole-4-carboxylic acid

Description:

Acetaldehyde, 5-methyloxazole-4-carboxylic acid, identified by its CAS number 32968-44-8, is a chemical compound that features both aldehyde and carboxylic acid functional groups, along with a heterocyclic oxazole ring. This compound is characterized by its relatively low molecular weight and polar nature, which can influence its solubility in water and organic solvents. The presence of the oxazole ring contributes to its potential biological activity, as heterocycles often play significant roles in medicinal chemistry. Acetaldehyde derivatives are known for their reactivity, particularly in condensation reactions and as intermediates in various synthetic pathways. The compound may exhibit specific properties such as volatility and a distinctive odor, typical of aldehydes. Additionally, its structural features suggest potential applications in pharmaceuticals or agrochemicals, although specific uses would depend on further research into its reactivity and biological effects. Safety data should be consulted for handling and exposure guidelines, as compounds with aldehyde groups can be irritants and may pose health risks.

Formula: C₇H₉NO₄

InChI: InChI=1/C5H5NO3.C2H4O/c1-3-4(5(7)8)6-2-9-3;1-2-3/h2H,1H3,(H,7,8);2H,1H3

SMILES: Cc1c(C(=O)O)nco1.CC=O

Synonyms:

• 5-Methyl-1,3-oxazole-4-carboxylic acid - acetaldehyde (1:1)
• 5-Methyl-4-oxazolcarbonsaeure-ethylester
• Ethyl 5-Methyl-4-oxazolecarboxylate

Ethyl 5-methyloxazole-4-carboxylate

CAS: 32968-44-8

Formula: C₇H₉NO₃

Purity: 95%

Color and Shape: Liquid

Molecular weight: 155.1513

Ref: IN-DA00CJZV

ethyl 5-methyl-1,3-oxazole-4-carboxylate

CAS: 32968-44-8

ethyl 5-methyl-1,3-oxazole-4-carboxylate

Purity: 95%

Molecular weight: 155.15g/mol

Ref: 54-OR910383

Ethyl 5-Methyloxazole-4-carboxylate

CAS: 32968-44-8

Formula: C₇H₉NO₃

Purity: 97%(GC-MS);RG

Color and Shape: Liquid, Clear

Molecular weight: 155.153

Ref: 10-F066985