86126-32-1 Usage
Uses
Used in Organic Synthesis:
1H-Indene, 2,3-dihydro-1,1,3-trimethyl-5-nitro-3-(4-nitrophenyl)is used as a building block in organic synthesis for the creation of more complex molecules. Its unique structure and functional groups make it a potentially valuable intermediate in the synthesis of various organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1H-Indene, 2,3-dihydro-1,1,3-trimethyl-5-nitro-3-(4-nitrophenyl)is used as a starting material for the development of new drugs. Its molecular structure, which includes nitro and methyl groups, may offer opportunities for medicinal chemists to explore its potential as a therapeutic agent or to modify it for improved pharmacological properties.
Used in Dye and Pigment Development:
Due to its distinct molecular structure and the presence of chromophoric groups, 1H-Indene, 2,3-dihydro-1,1,3-trimethyl-5-nitro-3-(4-nitrophenyl)has potential applications in the development of dyes and pigments. It may be utilized to create new colorants for various industrial applications, including textiles, plastics, and printing inks.
Used in Industrial Product Development:
The unique structure of 1H-Indene, 2,3-dihydro-1,1,3-trimethyl-5-nitro-3-(4-nitrophenyl)also suggests potential uses in the development of other industrial products. Its properties could be harnessed in the creation of new materials with specific characteristics, such as improved stability, reactivity, or other desirable attributes for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 86126-32-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,2 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86126-32:
(7*8)+(6*6)+(5*1)+(4*2)+(3*6)+(2*3)+(1*2)=131
131 % 10 = 1
So 86126-32-1 is a valid CAS Registry Number.
86126-32-1Relevant academic research and scientific papers
Method for synthesizing indane structure-containing compound
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Paragraph 0080-0120, (2020/08/18)
The invention provides a method for synthesizing an indane structure-containing compound, which comprises the following steps: 1) in the presence of a solid acid catalyst, carrying out a nitration reaction on an indane compound of a compound as shown in a general formula (I) to obtain compounds as shown in a general formula (II) and a general formula (III); and 2) in the presence of a reducing agent, performing a reduction reaction on the compounds represented by the general formula (II) and the general formula (III) to obtain compounds represented by the general formula (IV) and the general formula (V); wherein in the general formulas (I), (II), (III), (IV) and (V), R1, R2, R3 and R4 are independently hydrogen, C1-4 alkyl, C1-4 alkoxy, halogen, hydroxyl or carboxyl.
Separation and crystal structure of two isomeric of 1,3,3-trimethyl-5- nitro-3-(4-nitrophenyl)-2,3-dihydro-1H-indene and 1,3,3-trimethyl-5-nitro-1-(4- nitrophenyl)-2,3-dihydro-1H-indene
Wang,Wu,Shao,Men,Gao
, p. 399 - 402 (2014/06/09)
The isomers, 1,3,3-trimethyl-5-nitro-3-(4-nitrophenyl)-2,3-dihydro-1H- indene (1) and 1,3,3-trimethyl-5-nitro-1-(4-nitrophenyl)-2,3-dihydro-1H-indene (2), have been prepared and separated effectively. Their crystal structures can not be confirmed by the r
Phenylindane diamine mixture and epoxy resin therewith
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, (2008/06/13)
A mixture of phenylindane diamines is prepared by a process comprising acid-catalyzed dimerization of α-methylstyrene and subsequent nitration and reduction of the phenylindane reaction product. This phenylindane diamine mixture is useful in polymide polymers and as a curing agent for epoxy resins.
