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2,5-dimethylphenyl formate is an organic compound with the chemical formula C10H12O2. It is a colorless to pale yellow liquid with a fruity, floral odor. This ester is formed by the reaction of 2,5-dimethylphenol and formic acid, and it is commonly used as a fragrance ingredient in various consumer products, such as perfumes, cosmetics, and detergents. The compound has a molecular weight of 164.20 g/mol and is characterized by its two methyl groups attached to the phenyl ring at the 2nd and 5th positions, which contribute to its unique scent profile. It is also known for its low toxicity and is generally recognized as safe for use in fragrances.

1864-99-9

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1864-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1864-99-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,6 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1864-99:
(6*1)+(5*8)+(4*6)+(3*4)+(2*9)+(1*9)=109
109 % 10 = 9
So 1864-99-9 is a valid CAS Registry Number.

1864-99-9Relevant academic research and scientific papers

An expedient synthesis of ellipticine via Suzuki-Miyaura coupling

Konakahara, Takeo,Kiran,Okuno, Yuri,Ikeda, Reiko,Sakai, Norio

, p. 2335 - 2338 (2010)

A simple and efficient total synthesis of ellipticine was developed via the Suzuki-Miyaura coupling of sterically sensitive 2-hydroxybenzeneboronic acid with a multifunctional aryl halide using Pd(OAc)2 as a catalyst and Cu(OAc)2·H2O as an additive in DMSO/H2O as a key step followed by double N-arylation and cyclization.

Process for preparing an aryl formate and an aromatic carboxylic acid

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Page 10, (2008/06/13)

A method of producing aryl formate by oxidizing the aromatic aldehyde in an organic solvent having substantially no ability of dissolving water with performic acid generated in situ in the reaction system from the reaction between formic acid and hydrogen peroxide. Optionally the method comprises a second step for decomposing the aryl formate to a phenol compound. This second step may be performed by thermally decomposing the aryl formate to the phenol compound and carbon monoxide at 110 to 350°C in liquid phase in the presence of an alkali metal compound.

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