816-74-0 Usage
Uses
Used in Adhesives Industry:
Methallyl methacrylate is used as a monomer in the production of adhesives for its excellent adhesion properties, providing strong bonds between various materials.
Used in Coatings Industry:
Methallyl methacrylate is used as a component in the formulation of coatings due to its heat and chemical resistance, enhancing the durability and performance of the coatings in various applications.
Used in Textile Industry:
Methallyl methacrylate is used in the manufacturing of textiles to improve their resistance to heat and chemicals, making them suitable for industrial and commercial applications.
Safety Precautions:
It is important to handle methallyl methacrylate with care, as it can be irritating to the skin, eyes, and respiratory system, and may cause allergic reactions in some people. Proper safety protocols should be followed when working with this chemical to minimize potential health hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 816-74-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 816-74:
(5*8)+(4*1)+(3*6)+(2*7)+(1*4)=80
80 % 10 = 0
So 816-74-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O2/c1-6(2)5-10-8(9)7(3)4/h1,3,5H2,2,4H3
816-74-0Relevant articles and documents
METHOD FOR PRODUCING A HOMOGENEOUS CATALYST FOR THE TISHCHENKO REACTION
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Paragraph 0057; 0058; 0060-0062, (2020/06/07)
The invention relates to a process for preparing a carboxylic ester by reacting an aldehyde in the presence of an aluminum alkoxide, wherein the aluminum alkoxide is obtained either by reacting an aluminum hydride with an aldehyde or by reacting a different aluminum alkoxide with a carboxylic ester.
Method for preparing carboxylic esters from aldehydes
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Paragraph 0065-0066, (2018/12/04)
A method can prepare a carboxylic ester. The method includes reacting an aldehyde in the presence of an aluminium alkoxide applied to a support material.
Selective enzymatic epoxidation of dienes: Generation of functional enantiomerically enriched diene monoepoxy monomers
Hu, Shanghui,Gupta, Pankaj,Prasad, Ashok K,Gross, Richard A,Parmar, Virinder S
, p. 6763 - 6766 (2007/10/03)
Enantiomerically enriched diene monoepoxides were selectively synthesized using oxidases from Pseudomonas sp. and chloroperoxidase from Caldariomyces fumago. These monoepoxides are useful monomers for generating functional chiral polymeric materials.
