4801-39-2

Basic information

• Product Name: 2-AMINOACETANILIDEHYDROCHLORIDE
• Synonyms: 2-AMINOACETANILIDEHYDROCHLORIDE;N1-phenylglycinamide hydrochloride;2-AMINO-N-PHENYLACETAMIDE HCL
• CAS NO: 4801-39-2
• Molecular Formula: C₈H₁₀N₂O*ClH
• Molecular Weight: 186.64
• Mol File: 4801-39-2.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 361.5°C at 760 mmHg
• Flash Point: 172.4°C
• Appearance: /
• Vapor Pressure: 2.06E-05mmHg at 25°C
• CAS DataBase Reference: 2-AMINOACETANILIDEHYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINOACETANILIDEHYDROCHLORIDE(4801-39-2)
• EPA Substance Registry System: 2-AMINOACETANILIDEHYDROCHLORIDE(4801-39-2)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 4801-39-2(Hazardous Substances Data)

Usage

General Description

Black solid.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

An amide, and acidic salt. In aqueous solution, behaves as a weak acid. 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 are not available for 2-AMINOACETANILIDEHYDROCHLORIDE, but 2-AMINOACETANILIDEHYDROCHLORIDE is probably combustible.

InChI:InChI=1/C8H10N2O.ClH/c1-6(11)10-8-5-3-2-4-7(8)9;/h2-5H,9H2,1H3,(H,10,11);1H

Upstream product

• 62-53-3 aniline 
• 611-71-2 MANDELIC ACID 
• 21969-70-0 2-anilinoacetamide 
• 27904-92-3 N-glycyl>aniline 
• 6833-09-6 benzyl (2-oxo-2-(phenylamino)ethyl)carbamate 
• 42366-35-8 hydroxyimino-N-phenylacetamide 

Downstream Products

• 116005-80-2 4-(2-Amino-3-phenylcarbamoylmethyl-3,4-dihydro-quinazolin-6-yloxy)-N-cyclohexyl-N-methyl-butyramide; hydrobromide 
• 73376-17-7 PhCH₂O-DL-Ala-Gly-NHPh 
• 98554-96-2 N-phenyl-α-diazoacetamide 
• 68876-14-2 4-chloro-2-phenyl-[1,2,5]thiadiazol-3-one 
• 68876-32-4 3-chloro-2-phenyl-[1,2,5]thiadiazolium; chloride 
• 68876-36-8 N-phenyl-1,2,5-thiadiazole-3-amine 
• 93545-73-4 (Z)-7-{(1S,2R,3R,4R)-3-[(Phenylcarbamoylmethyl-amino)-methyl]-7-oxa-bicyclo[2.2.1]hept-2-yl}-hept-5-enoic acid 

Relevant articles and documents

N-transfer reagent and method for preparing the same and its application

Provided are a novel N-transfer reagent and a method for preparing the same and its application. The N-transfer reagent is represented by the following Formula (I): The various novel N-transfer reagents of the present invention can be quickly prepared by employing different nitrobenzene precursors. The N-transfer reagents can directly convert a variety of amino compounds into diazo compounds under mild conditions. Particularly, the N-transfer reagents can facilitate the synthesis of the diazo compounds. The application of synthesizing diazo compounds of the present invention can greatly decrease the difficulty in operation, increase the safety during experiments, reduce the cost of production and the environmental pollution, and enhance the industrial value of diazo compounds.

2-substituted-4-site functionalized N (O, S)-quinazoline derivative and application thereof

The invention relates to the technical field of medicine synthesis, and provides a 2-substituted-4-site functionalized N (O, S)-quinazoline derivative and an application thereof. The 2-substituted-4-site functionalized N (O, S)-quinazoline derivative prov

Process for preparation of an optically active amino acid amide

The present invention relates to a process for the preparation of optically active amino acid amide. L-amino and D-amino acid amides are mixed in the presence of 0.5-4 equivalents of an aldehyde, relative to the quantity of amino acid amide, in the presen