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Methyl 2-methylphenyl carbonate, also known as methyl o-tolyl carbonate, is an organic compound with the chemical formula C9H10O3. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 166.18 g/mol. methyl 2-methylphenyl carbonate is formed by the reaction of o-cresol (2-methylphenol) with methyl chloroformate, resulting in the formation of an ester linkage between the phenol and carbonate groups. Methyl 2-methylphenyl carbonate is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as a solvent and a reagent in various chemical reactions. Due to its reactivity and potential applications, it is essential to handle methyl 2-methylphenyl carbonate with care, following proper safety protocols.

1848-03-9

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1848-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1848-03-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1848-03:
(6*1)+(5*8)+(4*4)+(3*8)+(2*0)+(1*3)=89
89 % 10 = 9
So 1848-03-9 is a valid CAS Registry Number.

1848-03-9Downstream Products

1848-03-9Relevant academic research and scientific papers

Light-induced synthesis of unsymmetrical organic carbonates from alcohols, methanol and CO2under ambient conditions

Saini, Sandhya,Gour, Nand Kishor,Khan, Shafiur Rehman,Deka, Ramesh Chandra,Jain, Suman L.

supporting information, p. 12800 - 12803 (2021/12/13)

The present work describes the first visible light-assisted, metal-free and organic base 1,1,3,3-tetramethyl guanidine (TMG) mediated synthesis of unsymmetrical methyl aryl/alkyl carbonates from the reaction of alcohols, methanol, and CO2 in high to excel

Transesterification of dimethyl carbonate with phenol using Br?nsted and Lewis acidic ionic liquids

Deshmukh, Krishna M.,Qureshi, Ziyauddin S.,Dhake, Kishor P.,Bhanage, Bhalchandra M.

experimental part, p. 207 - 211 (2011/09/12)

Transesterification reaction of dimethyl carbonate with phenol to methylphenyl carbonate and diphenyl carbonate using dibutyltin oxide catalyst in conjunction with Br?nsted and Lewis acidic ionic liquids was studied. It was observed that the use of ionic liquids significantly enhances the yield of diphenyl carbonate. The ionic liquid having p-toluenesulfonate as anion and metal halide (e.g. ZnCl2) as Lewis acid precursor exhibited higher activity and selectivity for diphenyl carbonate formation. Furthermore, the Br?nsted and Lewis acidity of ionic liquids was measured by IR spectroscopy using pyridine as a probe and their Lewis acidity order was also determined.

Pentaalkylguanidines as etherification and esterification catalysts

Barcelo, Gerard,Grenouillat, Denis,Senet, Jean-Pierre,Sennyey, Gerard

, p. 1839 - 1848 (2007/10/02)

Several pentaalkylguanidines have been prepared and found to be superior catalysts for the preparation of aryl and aralkyl ethers from carbonates and for the methylation of phenols with dimethylcarbonate.They also act as effective catalysts for esterification of acids with alkyl chloroformates but not for the acetylation of tertiary alcohols with acetic anhydride.

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