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142596-50-7

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142596-50-7 Usage

General Description

3-Methoxy-2-Nitro Benzonitrile is a chemical compound with the molecular formula C8H6N2O3. It is a yellow crystalline solid that is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 3-Methoxy-2-Nitro Benzonitrile is known for its nitro and methoxy groups, which make it a versatile building block in organic chemistry. It is primarily used in the production of dyes and pigments, as well as in the development of other organic compounds. Additionally, 3-Methoxy-2-Nitro Benzonitrile is known for its potential toxicity and should be handled and used with caution in a controlled environment.

Check Digit Verification of cas no

The CAS Registry Mumber 142596-50-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,5,9 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 142596-50:
(8*1)+(7*4)+(6*2)+(5*5)+(4*9)+(3*6)+(2*5)+(1*0)=137
137 % 10 = 7
So 142596-50-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O3/c1-13-7-4-2-3-6(5-9)8(7)10(11)12/h2-4H,1H3

142596-50-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxy-2-nitrobenzonitrile

1.2 Other means of identification

Product number -
Other names 3-methoxy-2-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:142596-50-7 SDS

142596-50-7Relevant articles and documents

Quantum Tunneling Mediated Interfacial Synthesis of a Benzofuran Derivative

Paintner, Tobias,Bj?rk, Jonas,Du, Ping,Klyatskaya, Svetlana,Paszkiewicz, Mateusz,Hellwig, Raphael,Uphoff, Martin,?ner, Murat A.,Cuniberto, Edoardo,Deimel, Peter S.,Zhang, Yi-Qi,Palma, Carlos-Andres,Allegretti, Francesco,Ruben, Mario,Barth, Johannes V.,Klappenberger, Florian

, p. 11285 - 11290 (2019)

Reaction pathways involving quantum tunneling of protons are fundamental to chemistry and biology. They are responsible for essential aspects of interstellar synthesis, the degradation and isomerization of compounds, enzymatic activity, and protein dynami

Structure-activity relationship of a series of phenylureas linked to 4- phenylimidazole. Novel potent inhibitors of acyl-CoA:cholesterol O- acyltransferase with antiatherosclerotic activity. 2

Kimura,Watanabe,Matsui,Hayashi,Tanaka,Ohtsuka,Saeki,Kogushi,Kabayashi,Akasaka,Yamagishi,Saitou,Yamatsu

, p. 1641 - 1653 (2007/10/02)

In our continuing search to find systemically bioavailable ACAT (acyl- CoA:cholesterol O-acyl-transferase) inhibitors with more potent antiatherosclerotic effect than N-[2-(dimethylamino)-6-[3-(5-methyl-4- phenyl-1H-imidazol-1-yl)propoxy]phenyl]-N'-pentyl

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