Welcome to LookChem.com Sign In|Join Free
  • or
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.

2498-46-6

Post Buying Request

2498-46-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2498-46-6 Usage

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.

Check Digit Verification of cas no

The CAS Registry Mumber 2498-46-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,9 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2498-46:
(6*2)+(5*4)+(4*9)+(3*8)+(2*4)+(1*6)=106
106 % 10 = 6
So 2498-46-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2.ClH/c9-8(10)6-7-4-2-1-3-5-7;/h1-5H,6H2,(H3,9,10);1H

2498-46-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-PHENYLETHANIMIDAMIDE HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names 2-phenyl-acetamidine,hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2498-46-6 SDS

2498-46-6Relevant academic research and scientific papers

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

Kooistra, Floris B.,Leuning, Tessa M.,Maroto Martinez, Enrique,Hummelen, Jan C.

supporting information; scheme or table, p. 2097 - 2099 (2010/08/22)

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 Classical Cannabinoid Compounds and Related Methods of Use

-

Page/Page column 6-7, (2009/12/05)

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.

Pyrimidine Non-Classical Cannabinoid Compounds and Related Methods of Use

-

Page/Page column 6, (2009/12/05)

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.

Oxime glucokinase activators

-

Page/Page column 18, (2008/12/06)

Disclosed herein are pyrazole glucokinase activators of the formula (I): that are useful for the treatment of metabolic diseases and disorders.

REACTIVE INTERMEDIATES IN THE PHOTOLYSIS AND THERMOLYSIS OF 3-CHLORO-3-BENZYLDIAZIRINE

Liu, Michael T. H.,Chishti, Najmul H.,Tencer, Michael,Tomioka, Hideo,Izawa, Yasuji

, p. 887 - 892 (2007/10/02)

The photochemical and thermal decomposition of 3-chloro-3-benzyldiazirine have been studied in different reaction conditions.The decomposition gives rise to benzylchlorocarbene which can rearrange to E and Z chlorostyrene and/or react with the environment.In the presence of acetic acid the main product is 1-chloro-2-phenylethyl acetate.Experiments with acetic acid-d4 showed that some of the chlorostyrene is formed from the carbocation; other experiments conducted with tetramethylethylene as a carbene trapping agent show that the carbene is formed even in the presence of acetic acid.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2498-46-6