4415-87-6 Usage
Description
Cyclobutane-1,2,3,4-tetracarboxylic dianhydride is an organic compound with the chemical formula C8H2O5. It is a white to light yellow solid and is known for its unique chemical properties and diverse applications across various industries.
Uses
Used in Electronics Industry:
Cyclobutane-1,2,3,4-tetracarboxylic dianhydride is used as a monomer for the preparation of polyimide (PI), which possesses excellent electrical characteristics and optical properties. The PI film made from this material has a higher rate of cast visibility and can withstand high temperatures up to 340 degrees Celsius. Its performance is very good, making it an ideal material for the preparation of liquid crystal display films.
Used in Pharmaceutical and Biotechnology Industry:
Cyclobutane-1,2,3,4-tetracarboxylic dianhydride serves as a reactant for the preparation of biologically and pharmacologically active molecules. Its unique chemical structure allows for the development of new drugs and therapeutic agents with potential applications in various medical fields.
Used in Material Science:
Cyclobutane-1,2,3,4-tetracarboxylic dianhydride is used as a reactant for the preparation of photosensitive polyimide materials, which are essential for high-performance organic thin-film transistors. These materials have significant potential in the development of advanced electronic devices and components.
Used in Photonics:
Cyclobutane-1,2,3,4-tetracarboxylic dianhydride is utilized for selective crosslinking of polyimide in the fabrication of photonic devices. This process enhances the performance and stability of these devices, making them more suitable for various applications in the photonics industry.
Preparation
Preparation of 1,2,3,4- cyclobutanetetracarboxylic acid dianhydride (CBDA)To a 2L quartz glass photoreactor equipped with sixteen UV lamps (300nm) , a stirrer and a cooler were attached and 250ml of ethyl acetate and 100g of maleic anhydride were added thereto followed by stirring for complete mixing. To avoid an excessive temperature increase, an air-cooling type cooler was first run and then UV light was illuminated for a photoreaction for 24h?with stirring so as not to have the reactants adhered to the reactor walls. As a result, 71g of white solid was obtained. After the filtration, the white solid was dried for 24h?in a vacuum dryer at 60°C Thus-obtained solid was then added to acetic anhydride, dissolved therein and slowly heated to 150°C followed by the reaction for 24h . Hot reaction solution was filtered through a filter paper to remove impurities and kept in a freezer at the temperature of 0°C or less for recrystallization for 24h?to obtain a yellow solid. Thus-obtained solid was filtered and washed three times with 1,4-dioxane to remove acetic anhydride, and then dried in a vacuum oven at 60°C?for 48h?to obtain 64g of 1, 2, 3, 4 -cyclobutane tetracarboxylic acid dianhydride (CBDA) .
Check Digit Verification of cas no
The CAS Registry Mumber 4415-87-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,1 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4415-87:
(6*4)+(5*4)+(4*1)+(3*5)+(2*8)+(1*7)=86
86 % 10 = 6
So 4415-87-6 is a valid CAS Registry Number.
4415-87-6Relevant articles and documents
Development and Execution of a Production-Scale Continuous [2 + 2] Photocycloaddition
Beaver, Matthew G.,Zhang, En-Xuan,Liu, Zhi-Qing,Zheng, Song-Yuan,Wang, Bin,Lu, Jiang-Ping,Tao, Jian,Gonzalez, Miguel,Jones, Sian,Tedrow, Jason S.
, p. 2139 - 2146 (2020)
This article details the approach to large-scale production of cyclobutane 2 by the continuous-flow [2 + 2] photocycloaddition of maleic anhydride and ethylene, including (1) focused reaction optimization and development of a robust isolation protocol, (2) the approach to equipment design and process safety, and (3) the results of commissioning tests and production runs delivering the target compound at throughputs exceeding 5 kg/day.
AROMATIC DIAMINES WITH A PHOTOREACTIVE AROMATIC SIDE GROUP, POLYAMIC ACID PHOTO-ALIGNMENT LAYERS WITH THEM AND METHOD FOR PREPARING LIQUID CRYSTAL CELLS
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Page/Page column 27; 28, (2009/01/24)
The present invention relates to photo-alignment layers from polyamic acid with a photoreactive aromatic side group. More specifically, the present invention relates to novel polyamic acid photo-alignment layers prepared by the solution polymerization of acid dianhydrides which comprises alicyclic acid dianhydrides at certain ratio or more and aromatic diamines which comprises aromatic diamines with a photoreactive aromatic side group at certain ratio or more and the preparation method thereof, and the preparation method of aromatic diamines with novel aromatic side group. Said polyamic acid photo-alignment layers provide excellent heat- resistance, surface hardness, transparency and liquid crystal alignment property for polarized UV light.
Compounds, polymers, resin compositions and nonlinear optical devices
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, (2008/06/13)
The present invention provides, as heteroaromatic compounds made functional so as to be used for nonlinear optical materials, compounds represented by the following general formula (1), and also provides polymers obtained from these and nonlinear optical parts comprising such polymers. In the formula, Ar1 and Ar2 each represents a divalent aromatic group; R1, R2 and R3 each represents an atom or a group independently selected from a hydrogen atom or an alkyl group and an aromatic group; X1 represents a monovalent organic group; n represents an integer of 2 to 12; and Z1 and Z2 each represents a group independently selected from electron attractive functional groups.