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1-(2-METHOXY-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE, with the molecular formula C11H14O2S2, is a yellowish liquid chemical compound characterized by a molecular weight of 238.36 g/mol. It is recognized for its strong odor and is known to be an irritant to the skin, eyes, and respiratory system. 1-(2-METHOXY-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is also of interest due to its potential cytotoxic and anticancer properties, which are currently being explored for its application in medicinal chemistry.

37510-43-3

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37510-43-3 Usage

Uses

Used in Pharmaceutical Research:
1-(2-METHOXY-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is utilized as a precursor in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and chemical products.
Used in Organic Synthesis:
1-(2-METHOXY-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE serves as an essential intermediate in organic synthesis, playing a crucial role in the creation of different chemical entities.
Used in Medicinal Chemistry:
Due to its potential cytotoxic and anticancer properties, 1-(2-METHOXY-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is being investigated for its application in medicinal chemistry, with the aim of developing new therapeutic agents for cancer treatment.
Used in Chemical Research:
1-(2-METHOXY-PHENYL)-3,3-BIS-METHYLSULFANYL-PROPENONE is also employed in chemical research to study its properties, reactivity, and potential applications in various chemical processes and reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 37510-43-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,1 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37510-43:
(7*3)+(6*7)+(5*5)+(4*1)+(3*0)+(2*4)+(1*3)=103
103 % 10 = 3
So 37510-43-3 is a valid CAS Registry Number.

37510-43-3SDS

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-(2-methoxyphenyl)-3,3-bis(methylsulfanyl)prop-2-en-1-one

1.2 Other means of identification

Product number -
Other names -

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:37510-43-3 SDS

37510-43-3Downstream Products

37510-43-3Relevant academic research and scientific papers

Transition metal free synthesis of multifunctional thiomethylated-benzenes from aryl/heteroaryl/cyclopropyl methyl ketones

Panwar, Rahul,Althagafi, Ismail,Shally,Shaw, Ranjay,Elagamy, Amr,Shah, Chandan,Yadav, Pratik,Pratap, Ramendra

, (2020/04/28)

A base-promoted strategic synthesis of various functionalized thiomethylated-benzenes has been established from aryl/heteroaryl/cyclopropyl methyl ketone. We can directly access the thiomethylated-benzene nucleus embedded with diverse functional group by

A convenient base-mediated synthesis of 3-aryol-4-methyl (or benzyl)-2-methylthio furans from α-oxo ketene dithioacetals and propargyl alcohols via domino coupling/annulations

Yang, Xiaobing,Hu, Fangzhong,Di, Hongjing,Cheng, Xinxin,Li, Dan,Kan, Xiaoli,Zou, Xiaomao,Zhang, Qichun

supporting information, p. 8947 - 8951 (2014/12/11)

A convenient base-mediated strategy to synthesize 3-aryol-4-methyl (or benzyl)-2-methylthio furans 2 (trisubstituted furans) has been developed through the domino coupling/annulations between available α-oxo ketene dithioacetals 1 and propargyl alcohols.

Base mediated synthesis of α-aminated aroyl/acetylnaphthalenes through [4+2] annulations

Singh, Surjeet,Althagafi, Ismail,Yadav, Pratik,Panwar, Rahul,Kumar, Abhinav,Pratap, Ramendra

, p. 8879 - 8884 (2015/03/05)

We have developed a base promoted simple, efficient and alternative approach for the synthesis of 4-amino-3-aroyl//heteroaroyl/acetyl-2-methylsulfanyl-naphthalene-1-carbonitriles by reaction of easily accessible 3,3-bis(methylthio)-1-aryl/heteroaryl/acety

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