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1-Allyl-1-Tosylmethyl Isocyanide is a unique chemical compound that belongs to the class of organic compounds known as tosyl compounds. It is characterized by the presence of a sulfonyl group, which consists of sulfur bonded to two oxygen atoms and one carbon atom, attached to a toluene moiety. 1-ALLYL-1-TOSYLMETHYL ISOCYANIDE is particularly notable for its isocyanide group, where a carbon atom is bonded to a nitrogen atom and a carbene. The specific structure of 1-Allyl-1-Tosylmethyl Isocyanide, including its isocyanide group, contributes to its distinct properties, reactions, and potential uses in organic chemistry, such as in the formation of larger, complex structures.

58379-85-4

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58379-85-4 Usage

Uses

Used in Organic Chemistry:
1-Allyl-1-Tosylmethyl Isocyanide is used as a building block for the synthesis of more complex organic structures due to its unique isocyanide group and sulfonyl functionality. This allows for the creation of a wide range of compounds with various applications in different industries.
Used in Pharmaceutical Industry:
1-Allyl-1-Tosylmethyl Isocyanide is used as a key intermediate in the synthesis of pharmaceutical compounds. Its specific structural features enable the development of new drugs with potential therapeutic applications, such as in the treatment of various diseases and medical conditions.
Used in Material Science:
1-Allyl-1-Tosylmethyl Isocyanide is used as a precursor in the development of new materials with unique properties. Its incorporation into the synthesis process can lead to the creation of advanced materials with improved performance characteristics, such as enhanced stability, reactivity, or selectivity.
Used in Research and Development:
1-Allyl-1-Tosylmethyl Isocyanide is used as a research tool in academic and industrial laboratories. Its unique structure and reactivity make it an interesting subject for studying various chemical reactions and processes, which can contribute to the advancement of scientific knowledge and the development of new technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 58379-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,7 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58379-85:
(7*5)+(6*8)+(5*3)+(4*7)+(3*9)+(2*8)+(1*5)=174
174 % 10 = 4
So 58379-85-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO2S/c1-4-5-12(13-3)16(14,15)11-8-6-10(2)7-9-11/h4,6-9,12H,1,5H2,2H3

58379-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-isocyanobut-3-enylsulfonyl)-4-methylbenzene

1.2 Other means of identification

Product number -
Other names FD6013

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:58379-85-4 SDS

58379-85-4Relevant academic research and scientific papers

One-pot Van Leusen synthesis of 4,5-disubstituted oxazoles in ionic liquids

Wu, Bo,Wen, Jun,Zhang, Ji,Li, Jing,Xiang, Yong-Zhe,Yu, Xiao-Qi

experimental part, p. 500 - 504 (2009/08/07)

An efficient and mild protocol for the preparation of 4,5-disubstituted oxazoles through an improved one-pot van Leusen oxazole synthesis in ionic liquids is described. The oxazole products were prepared from tosylmethyl isocyanide (TosMIC), aliphatic hal

Synthesis and structure-activity relationship of a new series of COX-2 selective inhibitors: 1,5-Diarylimidazoles

Almansa, Carmen,Alfón, José,De Arriba, Alberto F.,Cavalcanti, Fernando L.,Escamilla, Ignasi,Gómez, Luis A.,Miralles, Agustí,Soliva, Robert,Bartrolí, Javier,Carceller, Elena,Merlos, Manuel,García-Rafanell, Julián

, p. 3463 - 3475 (2007/10/03)

The synthesis and the pharmacological activity of a series of 1,5-diarylimidazoles developed as potent and selective cyclooxygenase-2 (COX-2) inhibitors are described. The new compounds were evaluated both in vitro (COX-1 and COX-2 inhibition in human whole blood) and in vivo (carrageenan-induced paw edema, air-pouch, and hyperalgesia tests). Modification of all the positions of two regioisomeric imidazole cores led to the identification of 4-[4-chloro-5-(3-fluoro4-methoxyphenyl)imidazol-1-yl]benzenesulfonamide (UR-8880, 51f) as the best candidate, which is now undergoing Phase I clinical trials.

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