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1,4-Benzenedicarboxaldehyde, 2,3,5,6-tetramethyl- is an organic compound with the chemical formula C11H12O4. It is a derivative of benzene with two aldehyde groups (-CHO) at the 1st and 4th positions, and four methyl groups (-CH3) at the 2nd, 3rd, 5th, and 6th positions. 1,4-benzenedicarboxaldehyde, 2,3,5,6-tetramethyl- is also known as 2,3,5,6-tetramethyl-1,4-benzenedicarboxaldehyde or TMBD. It is a white crystalline solid with a melting point of 95-97°C. TMBD is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also used in the production of dyes and pigments. Due to its aldehyde groups, it can undergo various chemical reactions, such as oxidation, reduction, and condensation, making it a versatile building block in organic synthesis.

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  • 7072-01-7 Structure
  • Basic information

    1. Product Name: 1,4-benzenedicarboxaldehyde, 2,3,5,6-tetramethyl-
    2. Synonyms: 1,4-benzenedicarboxaldehyde, 2,3,5,6-tetramethyl-;2,3,5,6-tetramethylterephthalaldehyde;2,3,5,6-Tetramethyl-benzene-1,4-dicarbaldehyde
    3. CAS NO:7072-01-7
    4. Molecular Formula: C12H14O2
    5. Molecular Weight: 190.23836
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 7072-01-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 342°Cat760mmHg
    3. Flash Point: 128.3°C
    4. Appearance: /
    5. Density: 1.069g/cm3
    6. Vapor Pressure: 7.75E-05mmHg at 25°C
    7. Refractive Index: 1.578
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,4-benzenedicarboxaldehyde, 2,3,5,6-tetramethyl-(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,4-benzenedicarboxaldehyde, 2,3,5,6-tetramethyl-(7072-01-7)
    12. EPA Substance Registry System: 1,4-benzenedicarboxaldehyde, 2,3,5,6-tetramethyl-(7072-01-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 7072-01-7(Hazardous Substances Data)

7072-01-7 Usage

Explanation

1,4-Benzenedicarboxaldehyde, 2,3,5,6-tetramethylis derived from benzaldehyde, which is a simple aromatic aldehyde.

Explanation

Due to its powerful and pleasant odor, this compound is widely used in the fragrance industry to add a unique scent to various products.
4. Application in flavors

Explanation

The compound is also used in the production of flavors, adding a distinct taste to food and beverages.
5. Chemical intermediate

Explanation

It serves as a chemical intermediate in the synthesis of other organic compounds, which can be used in various industries.

Explanation

The unique chemical properties and structure of 1,4-benzenedicarboxaldehyde, 2,3,5,6-tetramethylmake it a candidate for potential use in the development of pharmaceuticals and agrochemicals.

Explanation

The compound has four methyl groups (CH3) attached to the benzene ring at positions 2, 3, 5, and 6, with a carboxylic acid group (COOH) at positions 1 and 4.

Explanation

The compound is typically found in a crystalline solid form, which can be used for various applications in the chemical and fragrance industries.

Explanation

The compound is known for its strong and appealing scent, making it a popular choice for use in the fragrance industry.

Explanation

1,4-Benzenedicarboxaldehyde, 2,3,5,6-tetramethylis soluble in organic solvents such as ethanol, acetone, and diethyl ether, which allows for easy handling and processing in various applications.

Common use

Fragrance ingredient in perfumes and personal care products

Potential applications

Pharmaceuticals and agrochemicals

Structure

2,3,5,6-tetramethyl substitution on a 1,4-benzenedicarboxaldehyde backbone

Appearance

Crystalline solid

Odor

Powerful and pleasant

Solubility

Soluble in organic solvents

Check Digit Verification of cas no

The CAS Registry Mumber 7072-01-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7072-01:
(6*7)+(5*0)+(4*7)+(3*2)+(2*0)+(1*1)=77
77 % 10 = 7
So 7072-01-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O2/c1-7-8(2)12(6-14)10(4)9(3)11(7)5-13/h5-6H,1-4H3

7072-01-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5,6-tetramethylterephthalaldehyde

1.2 Other means of identification

Product number -
Other names 2,3,5,6-tetramethylterephthalic dialdehyde

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7072-01-7 SDS

7072-01-7Relevant articles and documents

Aryllithiums with increasing steric crowding and lipophilicity prepared from chlorides in diethyl ether. the first directly prepared room-temperature-stable dilithioarenes

Screttas, Constantinos G.,Steele, Barry R.,Micha-Screttas, Maria,Heropoulos, Georgios A.

supporting information, p. 5680 - 5683 (2013/01/15)

A convenient procedure has been developed for the preparation of synthetically useful, room-temperature-stable aryllithiums starting from aryl chlorides and lithium metal. The method provides a route to aryllithiums which have previously not been accessible cleanly or could only be prepared by using more expensive starting materials.

Self-assembly and traveling wave ion mobility mass spectrometry analysis of hexacadmium macrocycles

Chan, Yi-Tsu,Li, Xiaopeng,Soler, Monica,Wang, Jin-Liang,Wesdemiotis, Chrys,Newkome, George R.

supporting information; experimental part, p. 16395 - 16397 (2010/02/15)

(Graph Presented) Self-assembly of 1,3-di(4′-terpyridinyl)arenes by using the labile tpy-Cd(II)-tpy (where tpy = 2,2′:6′,2″- terpyridine) connectivity afforded access to hexacadmium macrocycles in high yield. These supramolecular assemblies were character

Formylation and dichloromethylation as alternative directions of rieche reaction. A novel to the synthesis of sterically hindered aromatic dialdhydes

Yakubov, Alexander P.,Tsyganov, Dmitry V.,Belen'kii, Leonid I.,Krayushkin, Mikhail M.

, p. 3397 - 3404 (2007/10/02)

A previously unknown direction of Rieche reaction has been found: formylation of mesitylene, m-xylene, and durene with dichloromethyl methyl ether in the presence of aluminium trichloride and, to lesser extent, of titanium tetrachloride give the respective benzylidene dichlorides besides aldehydes. A novel approach to the synthesis of sterically hindered aromatic dialdehydes has been offered which involves the transformation of a monoaldehyde into the corresponding benzylidene dichloride, Rieche formylation of the latter, and hydrolysis of dichloromethyl aldehyde formed.

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.

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