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159010-67-0

2-(benzyloxy)-2-oxoethyl 3-({4-[2-(2-chloro-4,6-dinitrophenyl)diazen-1-yl]-5-acetamido-2-methoxyphenyl}amino)propanoate

CAS: 159010-67-0

Molecular Formula: C27H25ClN6O10

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159010-67-0 - Names and Identifiers

Name 2-(benzyloxy)-2-oxoethyl 3-({4-[2-(2-chloro-4,6-dinitrophenyl)diazen-1-yl]-5-acetamido-2-methoxyphenyl}amino)propanoate
Synonyms 2-(benzyloxy)-2-oxoethyl 3-({4-[2-(2-chloro-4,6-dinitrophenyl)diazen-1-yl]-5-acetamido-2-methoxyphenyl}amino)propanoate
β-Alanine, N-[5-(acetylamino)-4-[2-(2-chloro-4,6-dinitrophenyl)diazenyl]-2-methoxyphenyl]-, 2-oxo-2-(phenylmethoxy)ethyl ester
CAS 159010-67-0
EINECS 436-000-6

159010-67-0 - Physico-chemical Properties

Molecular FormulaC27H25ClN6O10
Molar Mass628.97
Density1.46±0.1 g/cm3(Predicted)
Boling Point860.4±65.0 °C(Predicted)
Vapor Presure0-0Pa at 25℃
AppearanceSolid:particulate/powder
pKa13.45±0.70(Predicted)

159010-67-0 - Introduction

2-(benzyloxy)-2-oxoethyl 3-({4-[2-(2-chloro-4,6-dinitrophenyl)diazen-1-yl]-} amino)propanoate is an organic compound, its molecular formula is C30H27ClN8O10 and its molecular weight is 677.03g/mol.

The compound has some of the following properties:

1. Appearance: 2-(benzyloxy)-2-oxoethyl 3-({4-[2-(2-chloro-4,6-dinitrophenyl)diazen-1-yl]-} amino)propanoate is a white solid.

2. Melting point: The melting point of this compound is about 180-182°C.

3. Solubility: 2-(benzyloxy)-2-oxoethyl 3-({4-[2-(2-chloro-4,6-dinitrophenyl)diazen-1-yl]-} amino)propanoate has good solubility in organic solvents.

2-(benzyloxy)-2-oxoethyl 3-({4-[2-(2-chloro-4,6-dinitrophenyl)diazen-1-yl]-} aniline) propoate has some applications in the field of chemistry, for example:

1. Dye: Because the compound has a colored molecular structure, it can be used as a raw material for organic dyes.

2. Biomarker: This compound can be used as a fluorescent marker in biological analysis to track certain biological molecules.

Preparation Method:

The preparation of 2-(benzyloxy)-2-oxoethyl 3-({4-[2-(2-chloro-4,6-dinitrophenyl)diazen-1-yl]-} amino) propoate can be completed by the following steps:

1.2-(benzyloxy)acetohydrazide is reacted with cuprous chloride to form 2-(benzyloxy)-N'-acetyl-1,2-diaziridin-3-ylidene.

2. The product obtained in the previous step is coupled with 2-methoxy-5-acetamidoaniline to generate 2-(benzyloxy)-2-oxoethyl 3-(2-methoxy-5-acetamidoanilino) propanoate.

3. Reaction of 2-(benzyloxy)-2-oxoethyl 3-(2-methoxy-5-acetamidoanilino) propanoate with nitrophenol and sodium nitrite yields 2-(benzyloxy)-2-oxoethyl 3-(2-methoxy-5-acetamidoanilino)-4,6-dinitrophenol.

4. Finally, 2-(benzyloxy)-2-oxoethyl 3-(2-methoxy-5-acetamidoanilino)-4,6-Dinitrophenol was reacted with sodium hydroxide and cuprous chloride, the final 2-(benzyloxy)-2-oxoethyl 3-({4-[2-(2-chloro-4,6-dinitrophenyl)diazen-1-yl]-} amino) propoate product was generated.

To sum up, 2-(benzyloxy)-2-oxoethyl 3-({4-[2-(2-chloro-4,6-dinitrophenyl)diazen-1-yl]-} amino)propanoate is an organic compound with special chemical properties and a wide range of applications.
Last Update:2024-04-10 22:29:15
159010-67-0
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