CAS 30866-24-1

ethyl 3-hydrazino-3-oxopropionate

Description:

Ethyl 3-hydrazino-3-oxopropionate, identified by its CAS number 30866-24-1, is an organic compound characterized by the presence of both hydrazine and ester functional groups. This compound features a propionate backbone, which contributes to its reactivity and potential applications in various chemical syntheses. The hydrazino group imparts unique properties, making it a candidate for use in pharmaceuticals and agrochemicals due to its ability to participate in condensation reactions and form hydrazones. Ethyl 3-hydrazino-3-oxopropionate is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It is soluble in polar solvents, which enhances its utility in organic synthesis. Safety data indicates that, like many hydrazine derivatives, it should be handled with care due to potential toxicity and reactivity. Overall, this compound serves as an important intermediate in the synthesis of more complex molecules, showcasing the versatility of hydrazine derivatives in organic chemistry.

Formula: C₅H₁₀N₂O₃

InChI: InChI=1/C5H10N2O3/c1-2-10-5(9)3-4(8)7-6/h2-3,6H2,1H3,(H,7,8)

SMILES: CCOC(=O)CC(=NN)O

Synonyms:

• Ethyl 3-Hydrazinyl-3-Oxopropanoate

Ethyl malonyl hydrazide

CAS: 30866-24-1

Formula: C₅H₁₀N₂O₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 146.1445

Ref: IN-DA0031IH

Ethyl 3-hydrazino-3-oxopropionate

CAS: 30866-24-1

Ethyl 3-hydrazino-3-oxopropionate

Purity: 96%

Molecular weight: 146.14g/mol

Ref: 54-OR322057

ETHYL MALONYL HYDRAZIDE

CAS: 30866-24-1

Formula: C₅H₁₀N₂O₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 146.146

Ref: 10-F470933

N1-Ethylmalonohydrazide

CAS: 30866-24-1

N1-Ethylmalonohydrazide (NEMH) is a hydroxylase ligand that has been shown to have anticancer activity. It binds to the active site of the enzyme, which converts 4-nitrophenylacetic acid into 4-aminophenol and carbon dioxide. NEMH is a precursor to the anticancer drug, melphalan. The anticancer activity of NEMH is due to its ability to crosslink DNA molecules, thereby inhibiting DNA synthesis. It also has an effect on the conformation of the molecule and may be responsible for its anti-cancer effects.

Formula: C₅H₁₀N₂O₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 146.14 g/mol

Ref: 3D-FBA86624