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1-<(2-methoxyethoxy)methoxy>-2-(phenylthio)cyclopropane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84547-20-6

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84547-20-6 Usage

Chemical structure

A complex structure containing a cyclopropane ring, a thioether group, and an ether group with a methoxyethoxy side chain.

Functional groups

Contains three different functional groups cyclopropane ring, thioether group, and ether group with a methoxyethoxy side chain.

Potential applications

May have potential applications in medicinal chemistry and materials science.

Reactivity

Due to its complex structure, it may exhibit potential reactivity and should be handled with care.

Toxicity

The complex structure may also lead to potential toxicity, so caution is advised during handling and use.

Further exploration

The compound warrants further exploration and study due to its fascinating and potentially versatile nature.

Check Digit Verification of cas no

The CAS Registry Mumber 84547-20-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,4 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 84547-20:
(7*8)+(6*4)+(5*5)+(4*4)+(3*7)+(2*2)+(1*0)=146
146 % 10 = 6
So 84547-20-6 is a valid CAS Registry Number.

84547-20-6Relevant articles and documents

A New and Convenient Synthetic Method for Cyclopropyl Phenyl Sulfides

Tanaka, Kazuhiko,Uneme, Hideki,Matsui, Shuichi,Kaji, Aritsune

, p. 2965 - 2972 (2007/10/02)

The reactions of a variety of 1,3-bis(phenylthio)propanes with butyllithium have been shown to produce cyclopropyl phenyl sulfides in good to high yields.A new and convenient in situ preparation of 1-lithiocyclopropyl phenyl sulfide can be readily carried out by treating 1,3-bis(phenylthio)propane with 2 equiv. of butyllithium at 0 degC in THF.The reaction with electrophiles proceeds in good yield.O-Aryl and O-alkyl S-cyclopropyl dithiocarbonates also can be prepared in good yields. 1,2-Bis(phenylthio)ethane was converted to phenyl vinyl sulfide on treatment with butyllithium, while 1,4-bis(phenylthio)butane was recovered unchanged by a similar treatment.

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