1037294-96-4 Usage
Uses
Used in Pharmaceutical Industry:
1-((4-Methoxyphenoxy)methyl)naphthalene is used as a reagent in the pharmaceutical industry for the synthesis of various drugs. Its unique chemical structure allows it to be a valuable component in the development of new medications.
Used in Agrochemical Industry:
In the agrochemical industry, 1-((4-Methoxyphenoxy)methyl)naphthalene is utilized as a reagent in the production of different agrochemicals, contributing to the development of more effective and safer products for agricultural use.
Used in Fragrance Industry:
1-((4-Methoxyphenoxy)methyl)naphthalene is used as a fragrance ingredient due to its aromatic and musky odor. It is incorporated into the formulation of various perfumes and scented products to enhance their overall fragrance profile.
Used in Organic Synthesis:
As a reagent in organic synthesis, 1-((4-Methoxyphenoxy)methyl)naphthalene is employed in the manufacture of other fine chemicals. Its versatility in chemical reactions makes it a valuable compound for creating a wide range of specialty chemicals used in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1037294-96-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,7,2,9 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1037294-96:
(9*1)+(8*0)+(7*3)+(6*7)+(5*2)+(4*9)+(3*4)+(2*9)+(1*6)=154
154 % 10 = 4
So 1037294-96-4 is a valid CAS Registry Number.
1037294-96-4Relevant academic research and scientific papers
Benzylic C-H activation and C-O bond formation via aryl to benzylic 1,4-palladium migrations
Kesharwani, Tanay,Larock, Richard C.
, p. 6090 - 6102 (2008/09/21)
A procedure for benzylic C-H activation has been developed using a palladium 1,4-aryl to benzylic migration as a key step. Carboxylates and phenoxides readily trap the resulting benzylic palladium intermediates obtained from palladium 'through space' migration. Aryl bromides and iodides have been successfully employed in this reaction, furnishing moderate to good yields. The mechanism of this reaction has been studied by deuterium-labeling experiments, which suggest that the migration of palladium from an aryl to a benzylic position occurs reversibly. The reaction conditions developed for the migration process also oxidize the neighboring benzylic alcohols to the corresponding aldehydes and ketones.
