2498-46-6

Basic information

• Product Name: 2-PHENYLETHANIMIDAMIDE HYDROCHLORIDE
• Synonyms: 2-PHENYLETHANIMIDAMIDE HYDROCHLORIDE;2-PhenylacetiMidaMide hydrochloride;Benzeneethanimidamide, hydrochloride (1:1)
• CAS NO: 2498-46-6
• Molecular Formula: C₈H₁₀N₂*ClH
• Molecular Weight: 0
• EINECS: 604-604-1
• Product Categories: Phenyls & Phenyl-Het
• Mol File: 2498-46-6.mol
• Article Data: 6

Chemical Properties

• Melting Point: 145-147 °C
• Boiling Point: 279.6°C at 760 mmHg
• Flash Point: 122.9°C
• Appearance: /
• Vapor Pressure: 0.00306mmHg at 25°C
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility: DMSO (Slightly), Methanol (Slightly)
• CAS DataBase Reference: 2-PHENYLETHANIMIDAMIDE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PHENYLETHANIMIDAMIDE HYDROCHLORIDE(2498-46-6)
• EPA Substance Registry System: 2-PHENYLETHANIMIDAMIDE HYDROCHLORIDE(2498-46-6)

Safety Data

• Hazardous Substances Data: 2498-46-6(Hazardous Substances Data)

Usage

Description

2-Phenylacetimidamide Hydrochloride is an organic compound with the chemical formula C8H10N2·HCl. It is a derivative of phenylacetimidamide, featuring a hydrochloride salt form. 2-PHENYLETHANIMIDAMIDE HYDROCHLORIDE is known for its potential applications in the synthesis of various pharmaceutical compounds.

Uses

Used in Pharmaceutical Synthesis:
2-Phenylacetimidamide Hydrochloride is used as a key intermediate in the preparation of trifluoromethyl pyrimido[1,3]diazepine compounds. These compounds are of interest in the pharmaceutical industry due to their potential therapeutic properties, including possible applications in the treatment of various diseases and disorders.

InChI:InChI=1/C8H10N2.ClH/c9-8(10)6-7-4-2-1-3-5-7;/h1-5H,6H2,(H3,9,10);1H

Upstream product

• 5442-34-2 ethyl 2-phenylacetimidate hydrochloride 
• 140-29-4 phenylacetonitrile 

Downstream Products

• 14277-09-9 N-Butyl-phenylacetamidin 
• 69981-49-3 N-Dimethylaminoethyl-phenylacetamidin 
• 96675-97-7 N,N'-Bis-<3-dimethylamino-propyl>-benzamidin 
• 40840-09-3 C₃₂H₂₉N₃OP₂ 
• 13689-14-0 6-benzyl-2,2,4,4-tetraphenyl-2λ⁵,4λ⁵-[1,3,5,2,4]triazadiphosphinine 
• 69981-47-1 N-Benzyl-phenylacetamidin 
• 38452-96-9 6-benzyl-2,2,4,4-tetraphenyl-2λ⁵,4λ⁵-[1,5,2,4]diazadiphosphinine 
• 21419-05-6 4-amino-5-phenylpyrimidine 
• 91272-23-0 2-(benzyl)-5,6-pentamethylenepyrimidin-4(3H)-one 
• 91272-33-2 2-benzyl-5,6-hexamethylenepyrimidin-4(3H)-one 
• 91272-44-5 2-benzyl-5,6-decamethylenepyrimidin-4(3H)-one 
• 1168-28-1 2,6-dibenzyl-5,6,7,8-tetrahydro-3H-pyrido[4,3-d]pyrimidin-4-one 
• 16673-85-1 2-benzyl-6-methyl-4(3H)-pyrimidinone 
• 120095-91-2 2-(3-benzyl-1,2,4-thiadiazol-5-yl)quinoline 

Relevant articles and documents

Two new types of π-conjugation between a fullerene sphere and an addend

Diazirine addition reactions to C60, followed by an HCl elimination step, yielded [6,6] and [5,6] sp2 carbon bridged fullerenes. The [5,6] adducts (alkylidenehomofullerenes) are the first examples of fullerene structures where the ad

Pyrimidine Non-Classical Cannabinoid Compounds and Related Methods of Use

Disclosed are compounds of the formula I: wherein R1, R2, V, W, X, Y and Z can be as defined herein. The compounds can be used in the treatment of disorders mediated by the cannabinoid receptors.

Heterocyclic amplifiers of phleomycin. VII. Phenyl-, tolyl-, phenoxy- and benzyl-pyrimidines; also some carbocyclic analogues

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