74205-51-9 Usage
Uses
Used in Pharmaceutical Industry:
2-Ethoxyphenylacetonitrile is used as a building block in the synthesis of various drugs. Its role in the production of pharmaceuticals is crucial due to its ability to contribute to the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Ethoxyphenylacetonitrile serves as an intermediate in the creation of pesticides, playing a significant part in agricultural chemical production to protect crops and enhance yields.
Used in Perfume and Flavoring Industry:
2-Ethoxyphenylacetonitrile is also utilized as an intermediate in the manufacturing of perfumes and flavorings, adding to the complexity and variety of scents and tastes in consumer products.
It is important to handle 2-Ethoxyphenylacetonitrile with care, as it may pose health risks if ingested, inhaled, or comes into contact with the skin.
Check Digit Verification of cas no
The CAS Registry Mumber 74205-51-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,0 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74205-51:
(7*7)+(6*4)+(5*2)+(4*0)+(3*5)+(2*5)+(1*1)=109
109 % 10 = 9
So 74205-51-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO/c1-2-12-10-6-4-3-5-9(10)7-8-11/h3-6H,2,7H2,1H3
74205-51-9Relevant articles and documents
High diastereoselectivity in the yang photocyclization via remote hydrogen abstraction reaction
Jang, Mi,Park, Bong Ser
, p. 1509 - 1514 (2016/10/09)
1-Benzoyl-1-(o-alkoxyphenyl)cyclopropanes undergo Yang photocyclization to form dihydrobenzopyranols in a stereospecific manner. The cyclopropyl group at alpha position to carbonyls gives not only a bias in the most stable geometries of the starting ketones but also conformational restriction on geometries of biradical intermediates. More importantly, intramolecular hydrogen bonds seem to give an additional effect on conformational control of the biradical reactivity.
