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59104-19-7

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59104-19-7 Usage

General Description

2-(4-Chloro-phenoxy)-acetamidine hydrochloride is a chemical compound with the molecular formula C8H10ClN3O.HCl. It is a derivative of acetamidine and is used as a selective and reversible inhibitor of the Na+/H+ exchanger isoform 1 (NHE1). The compound has been studied for its potential use in the treatment of various diseases, including cancer, cardiovascular disorders, and inflammatory conditions. It has also been investigated for its potential role in enhancing the efficacy of chemotherapy drugs. As a hydrochloride salt, it is typically used in laboratory research settings and pharmaceutical development.

Check Digit Verification of cas no

The CAS Registry Mumber 59104-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,0 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59104-19:
(7*5)+(6*9)+(5*1)+(4*0)+(3*4)+(2*1)+(1*9)=117
117 % 10 = 7
So 59104-19-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9ClN2O.ClH/c9-6-1-3-7(4-2-6)12-5-8(10)11;/h1-4H,5H2,(H3,10,11);1H

59104-19-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenoxy)ethanimidamide,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:59104-19-7 SDS

59104-19-7Relevant articles and documents

EFFECT OF REMOTE HETEROATOM SUBSTITUENTS ON STEREOCHEMISTRY IN 1,2 H MIGRATION TO DIVALENT CARBON. EVIDENCE FOR " NEGATIVE " HYPERCONJUGATION OF CARBENE LONE PAIR

Tomioka, Hideo,Hayashi, Norihiro,Inoue, Noboru,Izawa, Yasuji

, p. 1651 - 1654 (2007/10/02)

Aryloxymethylchlorocarbene generated by photolysis of the corresponding diazirine afforded α-aryloxy-β-chloroalkene.The thermodynamically less stable Z-products are the major isomers and its content becomes dominant as more electron-withdrawing groups are

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