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ISOCYANO(4-METHOXYPHENYL)METHYL-4-METHYLPHENYL SULFONE is a chemical compound with the formula C16H15NO3S, characterized by the presence of both isocyanide and methylphenyl groups within its sulfone structure. This versatile molecule is utilized in organic synthesis and holds promise for the development of pharmaceuticals and agrochemicals, with its specific applications and properties contingent upon the context of its use.

263389-54-4

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263389-54-4 Usage

Uses

Used in Organic Synthesis:
ISOCYANO(4-METHOXYPHENYL)METHYL-4-METHYLPHENYL SULFONE is used as a key intermediate in organic synthesis for the creation of various chemical compounds. Its unique structure allows for the formation of a wide range of products through chemical reactions, making it a valuable component in the synthesis process.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ISOCYANO(4-METHOXYPHENYL)METHYL-4-METHYLPHENYL SULFONE is used as a building block for the development of new drugs. Its chemical properties enable it to be incorporated into the molecular structures of potential therapeutic agents, contributing to the discovery and design of novel pharmaceuticals.
Used in Agrochemical Industry:
ISOCYANO(4-METHOXYPHENYL)METHYL-4-METHYLPHENYL SULFONE also finds application in the agrochemical sector, where it is utilized in the synthesis of pesticides and other agricultural chemicals. Its role in this industry is to provide a foundation for the creation of compounds that can effectively protect crops and enhance agricultural productivity.

Check Digit Verification of cas no

The CAS Registry Mumber 263389-54-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,3,3,8 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 263389-54:
(8*2)+(7*6)+(6*3)+(5*3)+(4*8)+(3*9)+(2*5)+(1*4)=164
164 % 10 = 4
So 263389-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO3/c1-8(13)12-10(11(14)15)7-9-5-3-2-4-6-9/h2-7H,1H3,(H,12,13)(H,14,15)/p-1/b10-7+

263389-54-4SDS

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 1-[isocyano-(4-methoxyphenyl)methyl]sulfonyl-4-methylbenzene

1.2 Other means of identification

Product number -
Other names a-Tosyl-(4-methoxybenzyl)isocyanide

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:263389-54-4 SDS

263389-54-4Relevant academic research and scientific papers

A Structure-based Design Approach for Generating High Affinity BRD4 D1-Selective Chemical Probes

Cui, Huarui,Divakaran, Anand,Hoell, Zachariah J.,Ellingson, Mikael O.,Scholtz, Cole R.,Zahid, Huda,Johnson, Jorden A.,Griffith, Elizabeth C.,Gee, Clifford T.,Lee, Amani L.,Khanal, Shalil,Shi, Ke,Aihara, Hideki,Shah, Vijay H.,Lee, Richard E.,Harki, Daniel A.,Pomerantz, William C. K.

, p. 2342 - 2360 (2022/01/27)

Chemical probes for epigenetic proteins are essential tools for dissecting the molecular mechanisms for gene regulation and therapeutic development. The bromodomain and extra-terminal (BET) proteins are master transcriptional regulators. Despite promising

The base-free van Leusen reaction of cyclic imines on water: Synthesis of N-fused imidazo 6,11-dihydro β-carboline derivatives

Satyam, Killari,Murugesh,Suresh, Surisetti

, p. 5234 - 5238 (2019/06/07)

Construction of imidazoles has been demonstrated on water under base-free conditions. The reaction of dihydro β-carboline imines and p-toluenesulfonylmethyl isocyanides furnished the corresponding substituted N-fused imidazo 6,11-dihydro β-carboline derivatives in very good yields under ambient conditions. The use of deuterium oxide (D2O) as a solvent enabled the incorporation of deuterium isotopes in the imidazole ring.

Shape-selective fluorescent sensing ensemble using a tweezer-type metalloreceptor

Plante, Jeffrey P.,Glass, Timothy E.

, p. 2163 - 2166 (2007/10/03)

A fluorescent sensing ensemble for pyridine-derived compounds is described. The receptor portion of the ensemble is prepared from a bisimidazole pyridine which coordinates copper to form a well-defined cavity. Small heteroaromatic guests such as adenine b

An efficient method for the synthesis of substituted TosMIC precursors

Sisko, Joseph,Mellinger, Mark,Sheldrake, Peter W.,Baine, Neil H.

, p. 8113 - 8116 (2007/10/03)

Substituted tosylmethyl isocyanides (TosMICs) are useful reagents for which no general method of preparation is available. We describe here a high-yielding method for the synthesis of substituted tosylmethyl formamides, which are readily converted to the corresponding isocyanides.

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