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<(p-tert-Butylphenoxy)methyl>thiirane is a chemical compound with the molecular formula C11H16OS. It is a cyclic sulfide derivative, featuring a thiirane ring (a three-membered ring containing sulfur) and a p-tert-butylphenoxy group attached to the carbon atom adjacent to the sulfur. <(p-tert-Butylphenoxy)methyl>thiirane is known for its unique structure and potential applications in various chemical reactions and synthesis processes. Due to its stability and reactivity, it can be used as an intermediate in the preparation of other organic compounds, particularly those involving sulfur-containing functional groups. The compound's properties, such as its boiling point, melting point, and solubility, can be influenced by the presence of the p-tert-butylphenoxy group, which provides steric hindrance and affects its reactivity.

3210-65-9

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3210-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3210-65-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,1 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3210-65:
(6*3)+(5*2)+(4*1)+(3*0)+(2*6)+(1*5)=49
49 % 10 = 9
So 3210-65-9 is a valid CAS Registry Number.

3210-65-9Downstream Products

3210-65-9Relevant academic research and scientific papers

[Bmim]PF6: A novel and recyclable ionic liquid for conversion of oxiranes to thiiranes in aqueous media

Yadav,Reddy,Srinivas, Ch.,Rajasekhar, Reddy K.

, p. 2525 - 2527 (2003)

A variety of epoxides respond rapidly with potassium thiocyanate in [bmim]PF6-H2O (2:1) solvent system at room temperature under mild and convenient conditions to produce the corresponding thiiranes in high to quantitative yields. Enhanced rates, improved yields, and recyclability of ionic liquids are the remarkable features observed in ionic liquids (ILs). The use of ionic liquids for this transformation avoids the use of heavy metal halides as promoters and chlorinated hydrocarbons as solvents. The ionic liquid was recycled in five to six subsequent runs with gradual decrease in activity.

Green synthesis of thiiranes from oxiranes under solvent- and catalyst-free conditions

Akhlaghinia, Batool,Rahimizadeh, Mohammad,Eshghi, Hosein,Zhaleh, Sara,Rezazadeh, Soodabeh

experimental part, p. 351 - 361 (2012/08/27)

A simple and efficient method for the conversion of oxiranes to thiiranes using ammonium thiocyanate (NH4SCN) under solvent- and catalyst-free conditions is described. These conditions enable clean and fast conversion of oxiranes to the corresponding thiirane.

LiClO4 catalyzed mild and efficient method for the synthesis of thiiranes from oxiranes

Reddy, Ch. Sanjeeva,Nagavani

, p. 97 - 99 (2008/04/05)

Oxiranes are efficiently converted to the corresponding thiiranes by potassium thiocyanate in the presence of catalytic amounts of LiClO4 with excellent yields under mild and nonaqueous conditions.

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