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5418-11-1

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5418-11-1 Usage

Description

PHENYL TRANS-STYRYL SULFONE 99 is a high-purity chemical compound that features a phenyl group, a trans-styryl group, and a sulfone functional group. It is renowned for its stability and versatility, serving as a valuable building block in organic chemistry. PHENYL TRANS-STYRYL SULFONE 99 is instrumental in the production of a wide range of materials and products, such as plastics, pharmaceuticals, and in organic synthesis.

Uses

Used in Plastics Industry:
PHENYL TRANS-STYRYL SULFONE 99 is used as a key component in the production of various types of plastics. Its unique chemical structure and reactivity contribute to the development of plastics with enhanced properties, such as improved thermal stability and mechanical strength.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, PHENYL TRANS-STYRYL SULFONE 99 is utilized as an intermediate in the synthesis of potential drug candidates. Its distinctive chemical properties make it a promising compound for the development of new medications with novel therapeutic effects.
Used in Organic Synthesis:
PHENYL TRANS-STYRYL SULFONE 99 is employed as a versatile building block in organic synthesis. It is used to create a variety of organic compounds, which can be further utilized in different applications across various industries, including the production of specialty chemicals and materials with specific properties.

Check Digit Verification of cas no

The CAS Registry Mumber 5418-11-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5418-11:
(6*5)+(5*4)+(4*1)+(3*8)+(2*1)+(1*1)=81
81 % 10 = 1
So 5418-11-1 is a valid CAS Registry Number.

5418-11-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Phenyl trans-styryl sulfone

1.2 Other means of identification

Product number -
Other names Phenyl styryl sulfone

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:5418-11-1 SDS

5418-11-1Relevant articles and documents

Sodium iodide-mediated synthesis of vinyl sulfides and vinyl sulfones with solvent-controlled chemical selectivity

Liu, Congrong,Wu, Gongde,Xu, Jin

, p. 35156 - 35160 (2021/11/30)

Vinyl sulfides and vinyl sulfones are ubiquitous structures in organic chemistry because of their presence in natural and biologically active compounds and are very frequently encountered structural motifs in organic synthesis. Herein we report an efficie

Visible-light-mediated alkylation of 4-alkyl-1,4-dihydropyridines with alkenyl sulfones

Dong, Jianyang,Liu, Yuxiu,Wang, Qingmin,Yue, Fuyang

supporting information, p. 8924 - 8928 (2021/11/04)

Herein we report a mild, general protocol for visible-light-mediated alkylation of 4-alkyl-1,4-dihydropyridines with alkenyl sulfones. The protocol permits efficient functionalization of sulfones with a broad range of cyclic and acyclic secondary and tert

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Ding, Qi-Da,Si, Jin-Ping,Huang, Kun-Lin,Tian, Feng,Chen, Sheng-Chun,Feng, Xue-Jun,He, Ming-Yang,Chen, Qun

, p. 69 - 74 (2019/05/21)

Based on the acid-base mixed-ligand assembly strategy, a stable Mn(II)-based metal-organic framework (denoted as Mn-MOFs), containing 1-D Mn–O–C rod-shaped chains, was hydrothermally synthesized and structurally characterized. This material was demonstrated to be an efficient heterogeneous catalyst for the decarboxylative sulfonylation of cinnamic acids with sodium benzene sulfinates. Moreover, the Mn-MOF catalyst could be recycled up to six times with the retention of both catalytic activity and crystal structure.

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