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24588-72-5

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24588-72-5 Usage

Description

4-Methoxybenzaldehyde trimethylenedithioacetal is a chemical compound characterized by the molecular formula C12H14O2S2. It is a liquid at room temperature and is recognized for its strong odor. 4-Methoxybenzaldehyde trimethylenedithioacetal is primarily utilized as an organic synthesis intermediate, playing a crucial role in the production of various synthetic compounds, including pharmaceuticals, fragrances, and other fine chemicals. Its chemical properties contribute to its versatility and importance in a broad spectrum of industrial applications.

Uses

Used in Pharmaceutical Industry:
4-Methoxybenzaldehyde trimethylenedithioacetal serves as a key intermediate in the synthesis of pharmaceuticals, facilitating the creation of diverse medicinal compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Fragrance Industry:
In the fragrance industry, 4-Methoxybenzaldehyde trimethylenedithioacetal is employed as a precursor for the production of various scent compounds. Its strong odor makes it a valuable component in creating distinctive and long-lasting fragrances.
Used in Fine Chemicals Production:
4-Methoxybenzaldehyde trimethylenedithioacetal is utilized in the synthesis of fine chemicals, which are high-purity chemicals used in various applications such as research, chemical analysis, and the production of specialty products.
Used as a Building Block in Organic Synthesis:
Due to its chemical properties, 4-Methoxybenzaldehyde trimethylenedithioacetal acts as an important building block in organic synthesis, enabling the formation of a wide range of synthetic compounds for various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 24588-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,8 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24588-72:
(7*2)+(6*4)+(5*5)+(4*8)+(3*8)+(2*7)+(1*2)=135
135 % 10 = 5
So 24588-72-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H14OS2/c1-12-10-5-3-9(4-6-10)11-13-7-2-8-14-11/h3-6,11H,2,7-8H2,1H3

24588-72-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxyphenyl)-1,3-dithiane

1.2 Other means of identification

Product number -
Other names m-DITHIANE,2-(p-METHOXYPHENYL)

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:24588-72-5 SDS

24588-72-5Relevant articles and documents

PhIO-Mediated oxidative dethioacetalization/dethioketalization under water-free conditions

Du, Yunfei,Ouyang, Yaxin,Wang, Xi,Wang, Xiaofan,Yu, Zhenyang,Zhao, Bingyue,Zhao, Kang

, p. 48 - 65 (2021/06/16)

Treatment of thioacetals and thioketals with iodosobenzene in anhydrous DCM conveniently afforded the corresponding carbonyl compounds in high yields under water-free conditions. The mechanistic studies indicate that this dethioacetalization/dethioketalization process does not need water and the oxygen of the carbonyl products comes from the hypervalent iodine reagent.

Highly ordered mesoporous functionalized pyridinium protic ionic liquid framework as a highly efficient catalytic system in chemoselective thioacetalization of carbonyl compounds under solvent-free conditions

Karimi, Nafiseh,Luque, Rafael,Rajabi, Fatemeh,Voskressensky, Leonid

, (2021/10/04)

Dithioacetals are a well-known class of organic compounds as both protecting group for the carbonyl compounds and valuable synthons for organic synthesis. Polysiloxane acidic ionic liquids containing pyridinium trifluoroacetate salts (PMO-Py-IL) as organi

Dehydrative Glycosylation Enabled by a Comproportionation Reaction of 2-Aryl-1,3-dithiane 1-Oxide?

Cai, Lei,Zeng, Jing,Li, Ting,Xiao, Ying,Ma, Xiang,Xiao, Xiong,Zhang, Qin,Meng, Lingkui,Wan, Qian

, p. 43 - 49 (2019/11/28)

A new dehydrative glycosylation reaction has been established by capitalizing on the comproportionation reaction of 2-aryl-1,3-dithiane 1-oxides promoted by triflic anhydride (Tf2O). By wedding the high potency of thiophilic promoter system with the step efficiency of dehydrative glycosylation, this reagent underwent facile intermolecular oxothio acetalization with C1-hemiacetal donor to install a temporary leaving group, rendering a transient electrophilic center at the remote site to the anomeric position. The sulfenyl triflate tethered at the terminus concomitantly activated the sulfide intramolecularly to afford the oxocarbenium ion, thereby facilitating the title glycosylation. Aside from accommodating broad range functional groups and inactive hemiacetal substrates, the present activation protocol also proved expedient for 1,3-diol protection. Most importantly, this method further provided a fresh perspective for the application of sulfur chemistry to carbohydrate chemistry.

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