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2-(4-NITROPHENYL)ETHANIMIDAMIDE HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39695-96-0

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39695-96-0 Usage

Type of compound

Salt of 2-(4-nitrophenyl)ethanimidamide

Uses

Synthesis of various pharmaceutical and agricultural products

Receptor antagonism

Potent and selective antagonist of the dopamine D3 receptor

Potential treatment

Various neurological disorders such as Parkinson's disease and schizophrenia

Use in synthesis

Building block in the synthesis of various organic compounds

Locations

Research laboratories and chemical manufacturing facilities

Check Digit Verification of cas no

The CAS Registry Mumber 39695-96-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,9 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39695-96:
(7*3)+(6*9)+(5*6)+(4*9)+(3*5)+(2*9)+(1*6)=180
180 % 10 = 0
So 39695-96-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N3O2.ClH/c9-8(10)5-6-1-3-7(4-2-6)11(12)13;/h1-4H,5H2,(H3,9,10);1H

39695-96-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-nitrophenyl)ethanimidamide hydrochloride

1.2 Other means of identification

Product number -
Other names [1-amino-2-(4-nitrophenyl)ethylidene]azanium chloride

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:39695-96-0 SDS

39695-96-0Relevant academic research and scientific papers

ISOTOPICALLY ENRICHED PYRIMIDIN-5-YL ACETIC ACID DERIVATIVES AS CRTH2 ANTAGONISTS

-

Page/Page column 18, (2011/08/03)

Provided herein are 2H- and 13C-enriched compounds of formula (I) or (II); wherein R is as defined herein, and wherein at least one hydrogen atom, in certain embodiments, three or more hydrogen atoms, are deuterium atoms or at least one carbon atom is a carbon-13 atom. Also provided are pharmaceutical compositions and methods using the 2H- and 13C-enriched compounds, useful for treating CRTH2-related diseases or disorders such as, for example, asthma, allergic rhinitis, atopic dermatitis, allergic conjuvatitis, Churg-Strauss syndrome, sinusitis, basophilic leukemia, chronic urticaria or basophilic leukocytosis.

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

IMIDAZO[1,2-C]PYRIMIDINYLACETIC ACID DERIVATIVES

-

Page/Page column 37, (2008/06/13)

The present invention relates to an imidazo[1,2-c]pyrimidinylacetic acid derivative and salts thereof which is useful as an active ingredient of pharmaceutical preparations. The imidazo[1,2-c]pyrimidinylacetic acid derivative of the present invention has

Pyrimidinylacetic acid derivatives useful for the treatment of diseases mediated by CRTH2

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Page 23, (2008/06/13)

The present invention relates to a pyrimidinylacetic acid derivative of formula (1) wherein R1-R4 is defined herein, and salts thereof which is useful as an active ingredient of pharmaceutical preparations. The pyrimidinylacetic acid derivative of the present invention has excellent CRTH2 (G-protein-coupled chemoattractant receptor, expressed on Th2 cells) antagonistic activity and can be used for the prophylaxis and treatment of diseases associated with CRTH2 activity, in particular for the treatment of allergic diseases, such as ashtma, allergic rhinitis and allergic conjunctivitis; eosinophil-related diseases, such as Churg-Strauss syndrome and sinusitis; and basophil-related diseases, such as basophilic leukemia, chronic urticaria and basophilic leukocytosis in human and other mammals.

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