1985-37-1 Usage
Description
1-Phenyl-2,3-naphthalenedicarboxylic anhydride, also known as a polyaromatic small molecule dye, is a chemical compound derived from naphthalene. It possesses unique optical and electronic properties due to its aromatic structure, making it a versatile molecule for various applications.
Uses
Used in Dye Industry:
1-Phenyl-2,3-naphthalenedicarboxylic anhydride is used as a dye for its ability to impart color to various materials. Its polyaromatic structure allows for strong coloration and stability, making it suitable for use in the dye industry.
Used in Metabolite Research:
In the field of metabolomics, 1-Phenyl-2,3-naphthalenedicarboxylic anhydride serves as a valuable metabolite for studying the metabolic pathways and processes within living organisms. Its unique structure allows for the identification and quantification of specific metabolic markers, contributing to a better understanding of various biological functions and diseases.
Used in Pharmaceutical Industry:
1-Phenyl-2,3-naphthalenedicarboxylic anhydride can be utilized as an intermediate in the synthesis of various pharmaceutical compounds. Its aromatic structure and anhydride functionality make it a versatile building block for the development of new drugs with potential therapeutic applications.
Used in Material Science:
Due to its polyaromatic nature, 1-Phenyl-2,3-naphthalenedicarboxylic anhydride can be employed in the development of advanced materials with specific optical, electronic, or mechanical properties. It can be used as a component in the synthesis of polymers, composites, or other materials with tailored characteristics for various applications in the material science field.
Check Digit Verification of cas no
The CAS Registry Mumber 1985-37-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1985-37:
(6*1)+(5*9)+(4*8)+(3*5)+(2*3)+(1*7)=111
111 % 10 = 1
So 1985-37-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H10O3/c19-17-14-10-12-8-4-5-9-13(12)15(16(14)18(20)21-17)11-6-2-1-3-7-11/h1-10H
1985-37-1Relevant articles and documents
One-pot syntheses of blue-luminescent 4-aryl-1H-benzo[f]isoindole-1, 3(2H)-diones by T3P activation of 3-arylpropiolic acids
Deni?en, Melanie,Kraus, Alexander,Reiss, Guido J.,Müller, Thomas J.J.
supporting information, p. 2340 - 2351 (2017/11/16)
In situ activation of 3-arylpropiolic acids with T3P (n-propylphosphonic acid anhydride) initiates a domino reaction furnishing 4-arylnaphtho[2, 3-c]furan-1, 3-diones in excellent yields. Upon employing these anhydrides as reactive intermediates blue-lumi
1-phenyl -2,3-naphthalene carboxylic acid anhydride, and its process for synthesis of derivatives of
-
Paragraph 0010-0013, (2017/02/24)
The invention discloses a synthesis method of 1-phenyl-2,3-naphthalene dicarboxylic anhydride and derivatives thereof. The synthesis method is used for synthesizing the 1-phenyl-2,3-naphthalene dicarboxylic anhydride compounds under an alkali condition in
Phthalocyanines and related compounds: XXXIX. Synthesis of derivatives of some substituted 1-phenylnaphthalene-2,3-dicarboxylic acids
Donyagina,Luk''yanets
, p. 795 - 799 (2007/10/03)
Derivatives (dinitriles, anhydrides, imides, N-phenylimides) of substituted 1-phenylnaphthalene-2,3-dicarboxylic and 1-phenylphenanthrene-2,3-dicarboxylic acids were prepared by the reactions of 2-bromomethylbenzophenones with various dienophiles. Starting from these derivatives, gallium complexes of substituted tetra-1-phenyl-2,3-naphthalocyanines and tetra(1-phenyl-2,3-phenanthro) porphyrazine were synthesized. 2005 Pleiades Publishing, Inc.
