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2-Isocyano-1-methoxy-4-nitrobenzene is an organic compound characterized by its molecular formula C8H6N2O3. This chemical features a benzene ring with a nitro group at the 4-position, a methoxy group at the 1-position, and an isocyano group at the 2-position. The isocyano group, which is an isomer of the more common cyano group, is notable for its different electronic and steric properties. The compound is likely to be used in the synthesis of various organic compounds due to its reactive functional groups, which can participate in a range of chemical reactions. It is important to handle 2-isocyano-1-methoxy-4-nitrobenzene with care, as the presence of a nitro group can make it potentially explosive under certain conditions, and the isocyano group may pose inhalation risks.

1983-95-5

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1983-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1983-95-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1983-95:
(6*1)+(5*9)+(4*8)+(3*3)+(2*9)+(1*5)=115
115 % 10 = 5
So 1983-95-5 is a valid CAS Registry Number.

1983-95-5SDS

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-isocyano-1-methoxy-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names Benzene,2-isocyano-1-methoxy-4-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:1983-95-5 SDS

1983-95-5Relevant academic research and scientific papers

Facile Synthesis of N -Substituted Benzimidazoles

Kurhade, Santosh,Rossetti, Arianna,D?mling, Alexander

, p. 3713 - 3718 (2016)

A particularly mild and efficient one-pot synthesis of N-substituted benzimidazole derivatives was developed. 2-Fluoro-5-nitrophenylisocyanide reacts with a diverse set of primary amines to afford the respective products in moderate to very good yield (35-95%; 20 examples).

Novel hexakis(areneisonitrile)technetium(I) complexes as radioligands targeted to the multidrug resistance P-glycoprotein

Herman,Sharma,Kronauge,Barbarics,Herman,Piwnica- Worms

, p. 2955 - 2963 (2007/10/02)

Transport substrates and modulators of the human multidrug resistance (MDR1) P-glycoprotein (Pgp) are generally lipophilic cationic compounds, many with substituted aryl moieties. We sought to synthesize aromatic technetium isonitrile complexes to enable

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