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N-(3-amino-4-ethoxyphenyl)acetamide

Product Name
N-(3-amino-4-ethoxyphenyl)acetamide
CAS No.
17026-81-2
Chemical Name
N-(3-amino-4-ethoxyphenyl)acetamide
Synonyms
NCI-C01887;Ncgc00090849-01;AMINOETHOXYACETANILIDE;3'-AMINO-P-ACETOPHENETIDIDE;4'-Ethoxy-3'-aminoacetanilide;N-(3-amino-4-ethoxyphenyl)acetamide;1-Acetylamino-4-ethoxy-3-aminobenzene;Acetamide, N-(3-amino-4-ethoxyphenyl)-
CBNumber
CB5908224
Molecular Formula
C10H14N2O2
Formula Weight
194.23
MOL File
17026-81-2.mol
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N-(3-amino-4-ethoxyphenyl)acetamide Property

Boiling point:
330.68°C (rough estimate)
Density 
1.1444 (rough estimate)
refractive index 
1.5000 (estimate)
pka
14.27±0.70(Predicted)
EPA Substance Registry System
3-Amino-4-ethoxyacetanilide (17026-81-2)
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Safety

Hazardous Substances Data
17026-81-2(Hazardous Substances Data)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
S572012
Product name
3'-AMINO-P-ACETOPHENETIDIDE
Purity
Aldrich
Packaging
250mg
Price
$179
Updated
2024/03/01
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N-(3-amino-4-ethoxyphenyl)acetamide Chemical Properties,Usage,Production

General Description

Brown powder.

Air & Water Reactions

N-(3-amino-4-ethoxyphenyl)acetamide may be sensitive to air and light . Insoluble in water.

Reactivity Profile

An amine and amide. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Fire Hazard

Flash point data for N-(3-amino-4-ethoxyphenyl)acetamide are not available; however, N-(3-amino-4-ethoxyphenyl)acetamide is probably combustible.

N-(3-amino-4-ethoxyphenyl)acetamide Preparation Products And Raw materials

Raw materials

Preparation Products

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N-(3-amino-4-ethoxyphenyl)acetamide Suppliers

Alchem Pharmtech,Inc.
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8485655694
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Riedel-de Haen AG
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Waterstone Technology, LLC
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Parchem Trading Ltd.
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Parchem Trading Ltd.
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