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2,5-dimethylbenzene-1,4-diyl dibenzoate is a complex organic compound with the chemical formula C22H18O4. It is a derivative of benzene, featuring two methyl groups attached to the 2nd and 5th carbon atoms of the benzene ring. The compound is characterized by a central benzene ring with two benzoate groups attached at the 1st and 4th carbon positions, forming a linear structure. This molecule is known for its aromatic properties and is often used in the synthesis of various pharmaceuticals, dyes, and other organic compounds due to its unique structure and reactivity. The compound's molecular weight is 346.38 g/mol, and it is typically obtained as a white crystalline solid. Its chemical structure and properties make it a valuable intermediate in organic synthesis, particularly in the preparation of complex molecules that require the presence of multiple benzene rings.

7479-29-0

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7479-29-0 Usage

Physical appearance

Colorless, viscous liquid with a mild, sweet odor and a relatively low volatility

Solubility

Insoluble in water but miscible in organic solvents

Stability

High stability

Volatility

Low volatility

Compatibility

Excellent compatibility with a wide range of polymers

Uses

Commonly used as a plasticizer and UV stabilizer in various industrial applications, including the production of plastics, adhesives, and coatings. Also used in personal care products and cosmetics as a film-former and viscosity increasing agent.

Check Digit Verification of cas no

The CAS Registry Mumber 7479-29-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7479-29:
(6*7)+(5*4)+(4*7)+(3*9)+(2*2)+(1*9)=130
130 % 10 = 0
So 7479-29-0 is a valid CAS Registry Number.

7479-29-0Relevant academic research and scientific papers

A short and convenient chemical route to optically pure 2-methyl chromanmethanols. Total asymmetric synthesis of β-, γ-, and δ-tocotrienols

Couladouros, Elias A.,Moutsos, Vassilios I.,Lampropoulou, Maria,Little, James L.,Hyatt, John A.

, p. 6735 - 6741 (2008/02/11)

(Chemical Equation Presented) With use of inexpensive commercially available raw materials, chromanmethanol precursors to the natural β-, γ-, and δ-tocotrienols have been prepared in high yield. Enzymatic resolution afforded chiral chromanmethanols in high enantiomeric excess. Subsequent attachment of the farnesyl side chain was high yielding, thus allowing the preparation of asymmetric β-, γ-, and δ-tocotrienols in one final step wherein simultaneous deprotection of the phenol and removal of the sulfone group occurs. This chemistry provides the first synthesis of natural-series β-tocotrienol.

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