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89001-53-6

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89001-53-6 Usage

Chemical Properties

white to light yellow crystal powde

Check Digit Verification of cas no

The CAS Registry Mumber 89001-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,0 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89001-53:
(7*8)+(6*9)+(5*0)+(4*0)+(3*1)+(2*5)+(1*3)=126
126 % 10 = 6
So 89001-53-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O2/c1-6-4-8(10(11)12)3-2-7(6)5-9/h2-4H,1H3

89001-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-4-nitrobenzonitrile

1.2 Other means of identification

Product number -
Other names 2-methyl-4-nitro-benzonitrile

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:89001-53-6 SDS

89001-53-6Relevant articles and documents

Modified Merrifield resin-supported PCP pincer palladium nanoparticles as a new polymeric catalyst for cyanation of aryl iodides

Tamami, Bahman,Mohaghegh Nezhad, Molki,Ghasemi, Soheila,Farjadian, Fatemeh

, p. 123 - 128 (2016/01/26)

A new tridentate PCP pincer palladium (Pd) complex based on cross-linked Merrifield resin containing phosphinite ligand was synthesized and characterized. This polymeric catalyst was used in preparation of benzonitriles from different aryl iodides using potassium hexacyanoferrate (II) as a cyanide source. The presence of active metallic Pd in the catalyst was verified by X-ray power diffraction and X-ray photoelectron spectroscopy techniques. Transmission electron microscopy showed good dispersion of catalytic sites in the range of 30-50 nm. The catalyst is easily separated from reaction mixture and can be used for several times in repeating cycles without considerable loss of activity. The leaching of Pd from the support is negligible, which was confirmed by inductively coupled plasma-optical emission spectrometry and hot filtration test.

Aryl or N-heteroaryl Substituted Methanesulfonamide Derivatives as Vanilloid Receptor Ligands

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Paragraph 0498; 0500, (2013/04/10)

The invention relates to aryl or N-heteroaryl substituted methanesulfonamide derivatives as vanilloid receptor ligands, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.

AMINE SUBSTITUTED METHANESULFONAMIDE DERIVATIVES AS VANILLOID RECEPTOR LIGANDS

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Page/Page column 80, (2013/04/13)

The invention relates to amine substituted methanesulfonamide derivatives of formula (I) as vanilloid receptor ligands, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.

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