110452-35-2 Usage
Derivative of 1,3,5-benzenetricarboxaldehyde
Yes
Explanation
1,3,5-Benzenetricarboxaldehyde, 2-methylis a derivative of the parent compound 1,3,5-benzenetricarboxaldehyde, which means it has a similar structure but with a modification (in this case, a methyl group at the 2nd position).
Explanation
This compound is utilized in various industries due to its chemical properties, which make it suitable for creating dyes, pigments, and other organic compounds, including pharmaceuticals.
Explanation
Due to its strong odor, 1,3,5-Benzenetricarboxaldehyde, 2-methylis used as a flavoring agent in the food industry to enhance the taste and aroma of certain products.
Explanation
The chemical is known to be toxic, which means it can cause harm to humans and the environment if not handled properly. Precautions should be taken when working with this compound to minimize exposure and potential health risks.
Explanation
Due to its toxicity, it is essential to handle 1,3,5-Benzenetricarboxaldehyde, 2-methylwith care, using appropriate safety measures such as gloves, eye protection, and proper ventilation to minimize the risk of exposure.
Usage
Production of dyes and pigments, synthesis of pharmaceuticals and other organic compounds
Application in the food industry
Flavoring agent
Toxicity
Considered toxic
Handling
Handle with care
Check Digit Verification of cas no
The CAS Registry Mumber 110452-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,4,5 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 110452-35:
(8*1)+(7*1)+(6*0)+(5*4)+(4*5)+(3*2)+(2*3)+(1*5)=72
72 % 10 = 2
So 110452-35-2 is a valid CAS Registry Number.
110452-35-2Relevant articles and documents
Conversion of 1,4-Dihydrobenzoic Acids to Polyformylbenzenes under Vilsmeier Reaction Conditions
Raju, B.,Krishna Rao, G. S.
, p. 197 - 199 (1987)
1,4-Dihydrobenzoic acids 1a-e are converted by a one-pot reaction to benzene- mono-, di- and tricarboxaldehydes under Vilsmeier reaction conditions in yields ranging from 6 to 65percent.The same methodology also serves to give naphthalene-1,3-dicarboxaldehyde (2f) from 1,4-dihydro-1-naphthoic acid (1f) in 91percent yield.
Vilsmeier Reaction Route to 4-Methylisophthalaldehyde
Sreenivasulu, M.,Rao, G. S. Krishna
, p. 581 - 582 (2007/10/02)
The formation of 4-methylisophthalaldehyde (II) from 4-methyl-3-penten-2-ol (IV) on Vilsmeier reaction is described and the mechanism of its formation presented.
