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2-(4-chloro-2-methylphenoxy)-N-(2-hydroxyethyl)acetamide is a complex organic compound with the molecular formula C11H14ClNO3. It is a derivative of acetamide, featuring a 4-chloro-2-methylphenoxy group attached to the 2-position of the acetamide backbone. 2-(4-chloro-2-methylphenoxy)-N-(2-hydroxyethyl)acetamide is characterized by its chlorinated phenyl ring, which contributes to its chemical properties. It is a white crystalline solid and is soluble in organic solvents. The presence of a hydroxyethyl group attached to the nitrogen atom of the acetamide suggests potential for hydrogen bonding and may influence its reactivity and solubility. This chemical is not commonly found in household products but may be used in specialized industrial applications or as an intermediate in the synthesis of other compounds. Due to its specific structure, it is important to handle it with care, as it may have specific safety and environmental considerations.

5809-83-6

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5809-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5809-83-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,0 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5809-83:
(6*5)+(5*8)+(4*0)+(3*9)+(2*8)+(1*3)=116
116 % 10 = 6
So 5809-83-6 is a valid CAS Registry Number.

5809-83-6Relevant academic research and scientific papers

Blue LED-Promoted Oxathiacetalization of Aldehydes and Ketones

Liu, You-Chen,Reddy, Daggula Mallikarjuna,Chen, Xin-An,Shieh, Yi-Chen,Lee, Chin-Fa

, p. 2542 - 2552 (2020/04/27)

In synthetic chemistry, the protection of aldehydes and ketones is crucial during multistep synthesis of complex molecules. Organic chemists have paid substantial attention to the synthesis of 1,3-oxathiolanes and 1,3-oxathianes because of their considera

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

supporting information, 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.

Use of sulfur containing initiators for anionic polymerization of monomers

-

, (2008/06/13)

An initiator is presented for anionically polymerizing monomers, to provide a functional head group on the polymer. A polymer having a functional head group derived from a sulfur containing anionic initiator, and optionally as additional functional group resulting from the use of a functional terminating reagent, coupling agent or linking agent is also provided. A method is presented for anionically polymerizing monomers comprising the step of polymerizing the monomers with a sulfur containing anionic initiator to provide a functional head group on the polymer. An elastomeric compound, comprising a functional polymer and filler is also described. Also provided is a tire having decreased rolling resistance resulting from a tire component containing a vulcanizable elastomeric compound.

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