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3-(2-oxiranylmethoxy)phenol, also known as 3-glycidyloxyphenol, is an organic compound with the chemical formula C9H10O3. It is a colorless to pale yellow liquid that is soluble in water and most organic solvents. 3-(2-oxiranylmethoxy)phenol is primarily used as a stabilizer for epoxy resins, which are widely employed in the production of composite materials, adhesives, and coatings. It functions by inhibiting the premature curing of epoxy resins, thus allowing for better control over the curing process and improving the final product's mechanical properties. 3-(2-oxiranylmethoxy)phenol is also known for its antioxidant properties, which can help protect materials from degradation due to exposure to heat, light, and oxygen.

4870-90-0

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4870-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4870-90-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4870-90:
(6*4)+(5*8)+(4*7)+(3*0)+(2*9)+(1*0)=110
110 % 10 = 0
So 4870-90-0 is a valid CAS Registry Number.

4870-90-0Relevant academic research and scientific papers

Practical, environment-benign and atom economic KOAc-catalysed deprotection of aryl TIPS ethers under mild fluoride-free conditions

Wang, Bing,Sun, Hui-Xia,Chen, Bo,Sun, Zhi-Hua

supporting information; experimental part, p. 1112 - 1114 (2010/04/23)

A KOAc-catalysed, fluoride-free protocol not only effects chemoselective deprotection of phenolic TIPS ethers without affecting acetal, ketal, carbamate, O-acetyl and aliphatic silyl ethers, but also improves its atom economy by recycling the silanol byproduct.

Synthesis and bovine β3-adrenergic agonistic activities of a novel series of aryloxypropanolamines

El Hadri,Nicolle,Guillaume,Leclerc,Pietri-Rouxel,Strosberg,Archimbault

, p. 517 - 522 (2007/10/03)

We synthesized a novel series of 21 aryloxypropanolamine compounds characterized by N-alkyl, aralkyl, and aryl substituents. The compounds showed potent β3-adrenergic agonistic activities in Chinese hamster ovary cells expressing the bovine β3-adrenoceptors with Kact and Ki values of 4.2 ± 3.0 nM and 459 ± 169 nM respectively, for the ligand with the best compromise between potency and affinity. Structure-activity relationships are discussed.

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