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22068-49-1

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22068-49-1 Usage

General Description

4-(1,3-Dithiolan-2-yl)phenol is an organic compound with the molecular formula C8H8OS2. It is a thiol-containing molecule that consists of a phenol group attached to a dithiolane ring. This chemical is commonly used as a stabilizer for polymerization processes and as a building block in the synthesis of various pharmaceuticals and agrochemicals. It is also known for its antioxidant properties and is used in the production of antioxidants for rubber and plastic materials. Additionally, 4-(1,3-Dithiolan-2-yl)phenol is used in the formulation of cosmetics and personal care products for its ability to protect against oxidative damage and improve the stability of formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 22068-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,6 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22068-49:
(7*2)+(6*2)+(5*0)+(4*6)+(3*8)+(2*4)+(1*9)=91
91 % 10 = 1
So 22068-49-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H10OS2/c10-8-3-1-7(2-4-8)9-11-5-6-12-9/h1-4,9-10H,5-6H2

22068-49-1 Well-known Company Product Price

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  • Alfa Aesar

  • (A17066)  4-(1,3-Dithiolan-2-yl)phenol, 97%   

  • 22068-49-1

  • 5g

  • 414.0CNY

  • Detail
  • Alfa Aesar

  • (A17066)  4-(1,3-Dithiolan-2-yl)phenol, 97%   

  • 22068-49-1

  • 25g

  • 1664.0CNY

  • Detail

22068-49-1SDS

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 4-(1,3-DITHIOLAN-2-YL)PHENOL

1.2 Other means of identification

Product number -
Other names p-(1,3-Dithiolan-2-yl)phenol

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:22068-49-1 SDS

22068-49-1Relevant articles and documents

Poly(N-bromobenzene-1,3-disulfonamide) and N,N,N′,N′- tetrabromobenzene-1,3-disulfonamide as a mild and efficient catalyst for chemoselective thioacetalization of carbonyl functions and transthioacetalization reactions

Veisi, Hojat,Ghorbani-Vaghei, Ramin,Dadamahaleh, Somayeh Akbari

, p. 699 - 705 (2011)

Poly(N-bromobenzene-1,3-disulfonamide) and N,N,N′,N′- tetrabromobenzene-1,3-disulfonamide are effective catalysts for chemoselective dithioacetalization of aldehydes in the presence of ketones under neutral conditions.

Phosphorylated Polyacrylonitrile Fibers as an Efficient and Greener Acetalization Catalyst

Xu, Gang,Cao, Jian,Zhao, Yali,Zheng, Lishuo,Tao, Minli,Zhang, Wenqin

supporting information, p. 2565 - 2575 (2017/09/25)

A novel solid acid catalyst (PANEAPF) is developed by immobilization of phosphoric acid on polyacrylonitrile fiber through covalent bonding. Various characterization techniques such as elemental analysis (EA), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), etc. are utilized to confirm the successful grafting and the stability of the fiber catalysts during application. PANEAPF shows high catalytic activity in the acetalization of aldehydes owing to the high utilization efficiency of its functionalized acid sites. In addition, the strong polarity micro-environment in the surface layers of PANEAPF make it highly suitable for catalytic application in both water and alcohol. Furthermore, the fiber catalyst can be applied to the acetalization of aldehydes in a continuous-flow process at room temperature, and shows excellent reactivity and superior recyclability (over 20 times). The many advantages of PANEAPF such as simple preparation, convenient regulation of acid amount, high durability, and eco-friendly process make it very attractive for fixed-bed reactors in the chemical industry.

Sulfonated polyanthracene-catalyzed highly efficient and chemoselective thioacetalization of carbonyl compounds and transthioacetalization of acetals and acylals

Fahid,Pourmousavi

, p. 16 - 29 (2015/10/20)

A straightforward and highly efficient procedure for the thioacetalization of a variety of aldehydes and transthioacetalization of acylals and acetals in good to excellent yields using catalytic amounts of sulfonated polyanthracene (S-PAT) is reported. Th

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