107796-84-9 Usage
Uses
Used in Organic Synthesis:
3-METHYL-3-(1-NAPHTHYL)PHTHALIDE is used as a synthetic building block for the creation of various organic compounds. Its chemical properties make it a versatile and valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-METHYL-3-(1-NAPHTHYL)PHTHALIDE is used as an intermediate in the development of new drugs. Its unique structure allows for the creation of novel molecules with potential therapeutic applications, contributing to the advancement of medical treatments.
Used in Agrochemical Industry:
3-METHYL-3-(1-NAPHTHYL)PHTHALIDE is also utilized in the agrochemical industry as a key component in the synthesis of new pesticides and other agricultural chemicals. Its integration into these products can lead to improved efficacy and reduced environmental impact.
Used in Specialty Chemicals:
3-METHYL-3-(1-NAPHTHYL)PHTHALIDE finds application in the production of specialty chemicals, such as dyes, pigments, and additives. Its distinctive properties enable the development of innovative products with enhanced performance characteristics, catering to the diverse needs of various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 107796-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,7,9 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 107796-84:
(8*1)+(7*0)+(6*7)+(5*7)+(4*9)+(3*6)+(2*8)+(1*4)=159
159 % 10 = 9
So 107796-84-9 is a valid CAS Registry Number.
107796-84-9Relevant academic research and scientific papers
Synthesis and Separation of Diastereomeric Imino Alcohol Derivatives of Chiral Phthalides: A Method for Assignment of Phthalide Absolute Configurations
Pirkle, William H.,Sowin, Thomas J.
, p. 3011 - 3017 (2007/10/02)
Representative members of a series of chiral type 1 phthalides were converted with Lawesson's reagent to the corresponding thionophthalides.On treatment with any of several configurationally known chiral amino alcohols in the presence of mercuric trifluoroacetate, diastereomeric imino alcohols are afforded.These prove to be readily separable by chromatography on either silica or chiral stationary phases derived from the N-3,5-dinitrobenzamides of (R)-phenylglycine or (S)-leucine.Both the elution order of these diastereomers from silica and their 1H NMR chemical shift differences may be related to relative/absolute configurations.Hydrolysis of the separated imino alcohol diastereomers affords configurationally established phthalide enantiomers.On the basis of their CD spectra, it is concluded that the enantiomers of the entire series of phthalides elute from the chiral stationary phases in a uniform order
