CAS 4114-31-2

Ethyl carbazate

Description:

Ethyl carbazate, with the CAS number 4114-31-2, is an organic compound characterized by its structure, which includes a carbazate functional group attached to an ethyl group. It is typically a colorless to pale yellow liquid with a faint odor. Ethyl carbazate is soluble in water and various organic solvents, making it versatile for different applications. The compound is known for its role as a reagent in organic synthesis, particularly in the formation of hydrazones and other nitrogen-containing compounds. It exhibits properties typical of carbazates, such as the ability to form stable complexes with metal ions. Ethyl carbazate is also of interest in medicinal chemistry, where it may exhibit biological activity, including potential anti-inflammatory and antimicrobial properties. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled. Overall, ethyl carbazate is a valuable compound in both industrial and research settings due to its reactivity and functional versatility.

Formula: C₃H₈N₂O₂

InChI: InChI=1/C3H8N2O2/c1-2-5(4)3(6)7/h2,4H2,1H3,(H,6,7)/p-1

InChI key: InChIKey=VYSYZMNJHYOXGN-UHFFFAOYSA-N

SMILES: C(OCC)(NN)=O

Synonyms:

• (Ethoxycarbonyl)hydrazine
• 1-(Ethoxycarbonyl)hydrazine
• 1-Carbethoxyhydrazine
• 1-Ethylhydrazinecarboxylate
• Carbazic acid, ethyl ester
• Carbethoxyhydrazine
• Carboethoxy hydrazine
• Ethoxy Formhydrazine
• Ethoxycarbonyl hydrazide
• Ethoxycarbonylhydrazine~Ethyl hydrazinocarboxylate
• Ethyl Hydrazinecarboxylate
• Ethyl carbazinate
• Ethyl hydrazine carboxylate:
• Ethyl hydrazinocarboxylate
• Ethyl hydrazinoformate
• Hydrazinecarboxylic acid, ethyl ester
• Hydrazinoformic acid ethyl ester
• Monocarbethoxyhydrazine
• N-(Carbethoxy)hydrazine
• N-(Ethoxycarbonyl)hydrazine
• NSC 2277
• NSC 52663
• Ethyl carbazate
• ethoxycarbonylhydrazide
• ethylcarbazinate
• AKOS 90785
• ETHOXY CARBONYLHYDRAZINE
• 1-(Carbethoxy)hydrazine
• ETHYL HYDRAZINE-1-CARBOXYLATE
• ethylhydrazinocarboxylate
• HYDRAZINOCARBOXYLIC ACID ETHYL ESTER

Ethyl carbazate, 97%

CAS: 4114-31-2

Prepare 4-phenylurazole from ethyl carbazate and then oxidize the urazole with gaseous dinitrogen tetroxide to yield 4-phenyl-1,2,4-tri- azoline-3,5-dione la. Modification of the ethyl carbazate procedure in which analytically pure monoalkylhydrazine hydrochlorides were isolated in greater than 90%

Formula: C₃H₈N₂O₂

Purity: 97%

Color and Shape: White to pink or white/pink, Crystals or powder or crystalline powder or lumps and/or chunks or fused solid

Molecular weight: 104.11

Ref: 02-A13860

Ethyl hydrazinecarboxylate

CAS: 4114-31-2

Formula: C₃H₈N₂O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 104.1078

Ref: IN-DA003OP3

Ethyl Carbazate

CAS: 4114-31-2

Formula: C₃H₈N₂O₂

Purity: >99.0%(T)

Color and Shape: White to Almost white powder to lump

Molecular weight: 104.11

Ref: 3B-C1097

Ethyl hydrazinecarboxylate

CAS: 4114-31-2

Ethyl hydrazinecarboxylate

Formula: C₃H₈N₂O₂

Purity: 98+%

Color and Shape: off-white crystalline solid

Molecular weight: 104.11g/mol

Ref: 54-OR25885

Ethyl carbazate

CAS: 4114-31-2

Formula: C₃H₈N₂O₂

Purity: ≥ 99.0%

Color and Shape: White to off-white crystals

Molecular weight: 104.11

Ref: 7W-GK4787

Ethyl hydrazinecarboxylate

CAS: 4114-31-2

Formula: C₃H₈N₂O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 104.109

Ref: 10-F208618

Ethyl Carbazate

Controlled Product

CAS: 4114-31-2

Applications Ethyl Carbazate is used in the synthesis of P1 aryl heterocycle-based thrombin inhibitors. It can be also used to prepare diazenedicarboxamides as inhibitors of alanylalanine ligase.
References Young, M., et al.: J. Med. Chem., 47, 2995 (2004); Kovac, A., et al.: Bioorg. Med. Chem. Lett., 17, 2047 (2007)

Formula: C₃H₈N₂O₂

Color and Shape: Neat

Molecular weight: 104.11

Ref: TR-E900950