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586-10-7

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586-10-7 Usage

General Description

3-Methoxy-5-nitroaniline, also known as MNMA, is a chemical compound with the molecular formula C7H8N2O3. It is a yellow crystalline solid with a melting point of 139-141 degrees Celsius. 3-METHOXY-5-NITROANILINE is used as an intermediate in the synthesis of various dyes and pigments, as well as in the production of pharmaceuticals. It is also employed as a chemical reagent in organic synthesis. 3-Methoxy-5-nitroaniline is considered to be toxic if ingested or inhaled and may cause skin and eye irritation upon contact. It should be handled and stored with proper safety precautions in place.

Check Digit Verification of cas no

The CAS Registry Mumber 586-10-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 586-10:
(5*5)+(4*8)+(3*6)+(2*1)+(1*0)=77
77 % 10 = 7
So 586-10-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O3/c1-12-7-3-5(8)2-6(4-7)9(10)11/h2-4H,8H2,1H3

586-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-METHOXY-5-NITROANILINE

1.2 Other means of identification

Product number -
Other names Benzenamine, 3-methoxy-5-nitro-

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:586-10-7 SDS

586-10-7Relevant articles and documents

Discovery of novel and potent leukotriene B4 receptor antagonists. Part 1

Goodnow, Robert A.,Hicks, Alexandra,Sidduri, Achyutharao,Kowalczyk, Agnieszka,Dominique, Romyr,Qiao, Qi,Lou, Jian Ping,Gillespie, Paul,Fotouhi, Nader,Tilley, Jefferson,Cohen, Noal,Choudhry, Satish,Cavallo, Gary,Tannu, Shahid A.,Ventre, Jessica D.,Lavelle, Danielle,Tare, Nadine S.,Oh, Hyesun,Lamb, Martin,Kurylko, Grazyna,Hamid, Rachid,Wright, Matthew B.,Pamidimukkala, Anjula,Egan, Thomas,Gubler, Ueli,Hoffman, Ann F.,Wei, Xin,Li, Ying L.,O'Neil, John,Marcano, Ruben,Pozzani, Karen,Molinaro, Tina,Santiago, Jennifer,Singer, Laura,Hargaden, Maureen,Moore, David,Catala, A. Robert,Chao, Lisa C. F.,Hermann, Gesine,Venkat, Radhika,Mancebo, Helena,Renzetti, Louis M.

experimental part, p. 3502 - 3516 (2010/09/08)

The inhibition of LTB4 binding to and activation of G-protein-coupled receptors BLT1 and BLT2 is the premise of a treatment for several inflammatory diseases. In a lead optimization effort starting with the leukotriene B4 (LTB4

Coupling compounds and hair dyeing compositions containg them

-

Page/Page column 9, (2008/06/13)

The present invention refers to Compound of the formula (I) wherein X is oxygen or sulphur; R1 is (C1-C4)-alkyl, (C1-C4)-alkyl which is substituted by hydroxy, (C1-C4)-alkoxy, hy

Substituted benzamide inhibitors of rhinovirus 3C protease

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Page column 12-13, (2010/01/31)

Nonpeptide benzamide-containing inhibitors of human rhinovirus (HRV) 3C protease are described.

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