529-65-7 Usage
Description
ACETYL-N-ETHYLANILIDE is an organic compound that is a white, crystalline solid with a faint odor. It is soluble in most organic solvents but insoluble in water and is combustible in nature.
Uses
1. Used as a substitute for camphor in nitrocellulose for its similar properties and ability to provide a pleasant odor.
2. Used in the chemical industry as a white, crystalline solid that can be easily dissolved in organic solvents, making it suitable for various chemical reactions and processes.
3. Utilized in the pharmaceutical industry due to its solubility in organic solvents, which can be beneficial for the formulation of various drugs and medications.
4. Employed in the fragrance industry for its faint odor, which can be used to create unique and pleasant scents in perfumes and other fragrance products.
5. Applied in the plastics and coatings industry as a component in the formulation of various products, taking advantage of its solubility and combustible properties.
Hazard
Toxic by ingestion, moderate fire risk.
Safety Profile
Moderately toxic by
ingestion. Can react with oxidizing materials.
To fight fire, use foam, CO2, dry chemical.
When heated to decomposition it emits
toxic fumes of NOx.
Check Digit Verification of cas no
The CAS Registry Mumber 529-65-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 529-65:
(5*5)+(4*2)+(3*9)+(2*6)+(1*5)=77
77 % 10 = 7
So 529-65-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO/c1-3-11(9(2)12)10-7-5-4-6-8-10/h4-8H,3H2,1-2H3
529-65-7Relevant articles and documents
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Pictet
, p. 3423 (1887)
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Meta Selective C-H Borylation of Sterically Biased and Unbiased Substrates Directed by Electrostatic Interaction
Chaturvedi, Jagriti,Haldar, Chabush,Bisht, Ranjana,Pandey, Gajanan,Chattopadhyay, Buddhadeb
, p. 7604 - 7611 (2021/05/26)
An electrostatically directed meta borylation of sterically biased and unbiased substrates is described. The borylation follows an electrostatic interaction between the partially positive and negative charges between the ligand and substrate. With this strategy, it has been demonstrated that a wide number of challenging substrates, especially 4-substituted substrates, can selectively be borylated at the meta position. Moreover, unsubstituted substrates also displayed excellent meta selectivity. The reaction employs a bench-stable ligand and proceeds at a milder temperature, precluding the need to synthesize a bulky and sophisticated ligand/template.
N-Alkylation of N-trimethylsilyl derivatives of lactams, amides, and imides with alkyl sulfonates
Baukov, Yu. I.,Kramarova, E. P.,Negrebetsky, Vad. V.,Shagina, A. D.,Shipov, A. G.,Tarasenko, D. V.
, p. 398 - 400 (2020/04/15)
The reaction of N-trimethylsilyl derivatives of amides and imides with alkyl sulfonates on heating affords the corresponding N-alkyl derivatives and trimethylsilyl sulfonates.