15138-39-3 Usage
Explanation
This is an alternative name for 1,3-Benzenedicarboxaldehyde, 2,4,6-trimethyl-, which is derived from its structure and properties.
Explanation
The compound consists of a benzene ring (a six-carbon ring with alternating single and double bonds) with three functional groups attached. Two of the carboxaldehyde groups are replaced by methyl groups, which are small alkyl groups consisting of one carbon atom bonded to three hydrogen atoms.
Explanation
Due to its versatile structure and ability to form stable chemical bonds, 1,3-Benzenedicarboxaldehyde, 2,4,6-trimethylis often used as a starting material for the synthesis of a wide range of organic compounds.
Explanation
The compound's ability to form stable and versatile chemical bonds makes it suitable for use in the production of various materials, including polymers (large molecules made up of repeating units), dyes (substances used to impart color to other materials), and pharmaceuticals (chemicals used for medicinal purposes).
Explanation
1,3-Benzenedicarboxaldehyde, 2,4,6-trimethylcan also be used as a fragrance ingredient in perfumes and other personal care products due to its pleasant odor.
Structure
Benzene ring with three carboxaldehyde groups and two methyl groups at positions 2, 4, and 6
Building Block
Used in the synthesis of various organic compounds
Applications
Production of polymers, dyes, and pharmaceuticals
Fragrance
Used in perfumes and personal care products
Check Digit Verification of cas no
The CAS Registry Mumber 15138-39-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,3 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15138-39:
(7*1)+(6*5)+(5*1)+(4*3)+(3*8)+(2*3)+(1*9)=93
93 % 10 = 3
So 15138-39-3 is a valid CAS Registry Number.
15138-39-3Relevant articles and documents
The synthesis of trianglimines: On the scope and limitations of the [3 + 3] cyclocondensation reaction between (1R,2R)-diaminocyclohexane and aromatic dicarboxaldehydes
Kuhnert, Nikolai,Rossignolo, Giulia M.,Lopez-Periago, Ana
, p. 1157 - 1170 (2003)
The synthesis of aromatic dicarboxaldehydes, using dilithiation methodology is described along with their reactivity, in the [3 + 3] cyclocondensation reaction, with (1R,2R)-diaminocyclohexane to give trianglimine macrocycles. The scope and limitations of the cyclocondensation reaction are studied and some comments on the properties of the novel macrocycles are made such as their conformation in solution and temperature dependent dynamic NMR behaviour.
Efficient photocyclization of o-alkylbenzaldehydes in the solid state: Direct observation of E-xylylenols en route to benzocyclobutenols
Moorthy,Mal,Natarajan,Venugopalan
, p. 7013 - 7019 (2007/10/03)
The photocyclization to benzocyclobutenols of o-alkyl aromatic aldehydes that are predestined for γ-hydrogen abstraction is found to occur efficiently in the solid state; in contrast, solution-phase photolysis is known to afford a mixture of several produ
SYNTHESIS OF STERICALLY HINDERED AROMATIC ALDEHYDES
Yakubov, A. P.,Tsyganov, D. V.,Belen'kii, L. I.,Krayushkin, M. M.
, p. 1427 - 1432 (2007/10/02)
Formylation of mesitylene, durene, and m-xylene derivatives containing electron-donor and electron-acceptor substituents by dichloromethyl methyl ether was studied in the presence of TiCl4.A series of functionally substituted sterically hindered benzaldehydes was prepared from the products of these reactions.
