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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
Molecular Weight:
194.23
MDL Number:
MFCD00026773
MOL File:
17026-81-2.mol
Last updated:2023-05-04 15:15:50

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

Boiling point 330.68°C (rough estimate)
Density 1.1444 (rough estimate)
refractive index 1.5000 (estimate)
pka 14.27±0.70(Predicted)
FDA UNII 8W076B0J2D
EPA Substance Registry System 3-Amino-4-ethoxyacetanilide (17026-81-2)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P

N-(3-amino-4-ethoxyphenyl)acetamide price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich S572012 3'-AMINO-P-ACETOPHENETIDIDE Aldrich 17026-81-2 250mg $179 2024-03-01 Buy
Product number Packaging Price Buy
S572012 250mg $179 Buy

N-(3-amino-4-ethoxyphenyl)acetamide Chemical Properties,Uses,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

Global( 11)Suppliers
Supplier Tel Email Country ProdList Advantage
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63687 58
SynAsst Chemical. 021-60343070 China 12740 55
Nanjing NingFan Pharm-Tech CO. LTD. 17368696818 China 1984 58
Shaanxi Xihua Chemical Industry Co., Ltd 17691182729 15529505138 1021@dideu.com China 9969 58
3'-AMINO-P-ACETOPHENETIDIDE N-(3-amino-4-ethoxyphenyl)acetamide AMINOETHOXYACETANILIDE 1-Acetylamino-4-ethoxy-3-aminobenzene 4'-Ethoxy-3'-aminoacetanilide NCI-C01887 Ncgc00090849-01 Acetamide, N-(3-amino-4-ethoxyphenyl)- 17026-81-2 Intermediates of Dyes and Pigments