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2,6-BIS(4-AZIDOBENZYLIDENE)CYCLOHEXANONE is a chemical compound characterized by its molecular formula C24H20N6O. It is a yellow crystalline solid known for its photoinitiating properties in polymerization processes. 2,6-BIS(4-AZIDOBENZYLIDENE)CYCLOHEXANONE features two azide functional groups and a cyclohexanone backbone, which contribute to its utility in crosslinking and photopatterning applications. Its photochemical properties and crosslinking capabilities render it an asset in the creation of advanced materials, such as photoresists, microelectronics, and three-dimensional (3D) printing. As a photoinitiator, it can trigger polymerization reactions upon exposure to ultraviolet light, positioning it as a key component in the development of photopolymer-based systems.

20237-98-3

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20237-98-3 Usage

Uses

Used in Photopolymerization Applications:
2,6-BIS(4-AZIDOBENZYLIDENE)CYCLOHEXANONE is used as a photoinitiator for initiating polymerization reactions upon exposure to ultraviolet light. This application is crucial in the development of photopolymer-based systems, where its ability to induce rapid curing of monomers and oligomers is highly valued.
Used in Advanced Material Development:
In the field of material science, 2,6-BIS(4-AZIDOBENZYLIDENE)CYCLOHEXANONE is used as a component in the creation of advanced materials such as photoresists, which are essential in the microelectronics industry for patterning processes. Its crosslinking properties are beneficial in enhancing the performance and stability of these materials.
Used in 3D Printing Industry:
2,6-BIS(4-AZIDOBENZYLIDENE)CYCLOHEXANONE is utilized as a photoinitiator in the 3D printing process, particularly in techniques that rely on photopolymerization. Its role in this industry is to facilitate the rapid solidification of polymers, enabling the precise and detailed construction of three-dimensional objects.
Used in Crosslinking and Photopatterning Applications:
2,6-BIS(4-AZIDOBENZYLIDENE)CYCLOHEXANONE is employed in crosslinking and photopatterning applications across various industries, where its ability to form covalent bonds upon exposure to light is leveraged to create complex and intricate patterns or structures with enhanced mechanical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 20237-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,3 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20237-98:
(7*2)+(6*0)+(5*2)+(4*3)+(3*7)+(2*9)+(1*8)=83
83 % 10 = 3
So 20237-98-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H16N6O/c21-25-23-18-8-4-14(5-9-18)12-16-2-1-3-17(20(16)27)13-15-6-10-19(11-7-15)24-26-22/h4-13H,1-3H2/b16-12+,17-13+

20237-98-3 Well-known Company Product Price

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  • TCI America

  • (B1110)  2,6-Bis(4-azidobenzylidene)cyclohexanone (wetted with ca. 30% Water) (unit weight on dry weight basis) [Research for Photosensitive Material]  >85.0%(HPLC)

  • 20237-98-3

  • 5g

  • 690.00CNY

  • Detail
  • TCI America

  • (B1110)  2,6-Bis(4-azidobenzylidene)cyclohexanone (wetted with ca. 30% Water) (unit weight on dry weight basis) [Research for Photosensitive Material]  >85.0%(HPLC)

  • 20237-98-3

  • 25g

  • 2,190.00CNY

  • Detail

20237-98-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-bis[(4-azidophenyl)methylidene]cyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 2,4-PENTANEDIOL DIACETATE---CLEAR LIQUID

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:20237-98-3 SDS

20237-98-3Downstream Products

20237-98-3Relevant academic research and scientific papers

Process for the preparation of azidobenzal compounds

-

, (2008/06/13)

A process for preparing a 2,6-bis-[(4-azidophenyl)methylene]-cyclohexanone of the formula STR1 wherein R is hydrogen or alkyl of 1-6 C atoms, comprises condensing a cyclohexanone of the formula STR2 wherein R is as defined above, with 4-aminobenzaldehyde,

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