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4,4'-(1,2-Diphenylethene-1,2-diyl)dianiline, commonly referred to as stilbene diamine, is a chemical compound characterized by its distinctive structure that features two benzene rings linked by a vinylene (ethylene) bridge, with amino (NH2) groups attached to each benzene ring. This versatile compound is recognized for its high thermal stability, excellent compatibility with a range of materials, and its capacity to enhance the color properties of various products. Its molecular structure also positions it as a valuable intermediate in the synthesis of more complex organic compounds.

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  • 99094-20-9 Structure
  • Basic information

    1. Product Name: NA
    2. Synonyms: DK7555;4,4'-(1,2-Diphenylethene-1,2-diyl)dianiline;4-[2-(4-aminophenyl)-1,2-diphenylethenyl]aniline;4,4'-(1,2-diphenyl-1,2-ethenediyl)bis-benzenamine
    3. CAS NO:99094-20-9
    4. Molecular Formula: C26H22N2
    5. Molecular Weight: 362.46628
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 99094-20-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 525.8±50.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.168±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 4.71±0.10(Predicted)
    10. CAS DataBase Reference: NA(CAS DataBase Reference)
    11. NIST Chemistry Reference: NA(99094-20-9)
    12. EPA Substance Registry System: NA(99094-20-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 99094-20-9(Hazardous Substances Data)

99094-20-9 Usage

Uses

Used in Dye and Pigment Production:
4,4'-(1,2-Diphenylethene-1,2-diyl)dianiline is utilized as a building block in the creation of dyes and pigments, leveraging its ability to impart vibrant and stable color characteristics to these products.
Used in Optical Brighteners and Fluorescent Dyes:
In the field of optical brighteners and fluorescent dyes, 4,4'-(1,2-Diphenylethene-1,2-diyl)dianiline serves as a key component, contributing to the development of products with enhanced luminescence and visibility.
Used in Polymeric Materials:
4,4'-(1,2-Diphenylethene-1,2-diyl)dianiline is employed as a component in polymeric materials, where its thermal stability and compatibility enhance the performance and durability of the final products.
Used in Chemical Synthesis:
As an intermediate in chemical synthesis, 4,4'-(1,2-Diphenylethene-1,2-diyl)dianiline is used for the production of other complex organic compounds, showcasing its versatility in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 99094-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,0,9 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 99094-20:
(7*9)+(6*9)+(5*0)+(4*9)+(3*4)+(2*2)+(1*0)=169
169 % 10 = 9
So 99094-20-9 is a valid CAS Registry Number.

99094-20-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(4-aminophenyl)-1,2-diphenylethenyl]aniline

1.2 Other means of identification

Product number -
Other names Benzenamine,4,4'-(1,2-diphenyl-1,2-ethenediyl)bis

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:99094-20-9 SDS

99094-20-9Downstream Products

99094-20-9Relevant articles and documents

Dramatic Differences in Aggregation-Induced Emission and Supramolecular Polymerizability of Tetraphenylethene-Based Stereoisomers

Peng, Hui-Qing,Zheng, Xiaoyan,Han, Ting,Kwok, Ryan T. K.,Lam, Jacky W. Y.,Huang, Xuhui,Tang, Ben Zhong

, p. 10150 - 10156 (2017)

Geometric (Z)- and (E)-isomers play important but different roles in life and material science. The design of new (Z)-/(E)- isomers and study of their properties, behaviors, and interactions are crucially important in molecular engineering. However, diffi

Stepwise enhancement of fluorescence induced by anion coordination and non-covalent interactions

Zhang, Dan,Zhao, Jie,Cao, Liping,Yang, Dong,Chen, Bozhong,Yu, Le,Yang, Xiao-Juan,Wu, Biao

, p. 76 - 80 (2021)

A multi-level regulation of fluorescence enhancement upon anion coordination and subsequent binding of a guest (methyl viologen) was presented by a bis-bis(urea)-decorated tetraphenylethene (TPE) ligand with an assembly-enhanced emission characteristic.

Oxidative evolution of Z / e -diaminotetraphenylethylene

Li, Xin,Liu, Xiangyang,Ran, Qichao,Zhuang, Yongbing

, p. 1960 - 1964 (2022/02/07)

We report that Z/E-diaminotetraphenylethylene (Z/E-2NH2-TPE) molecules suffer primarily from oxidative evolution rather than recognized isomerization. The oxide is separated and its structure is deciphered by single crystal X-ray diffraction. The oxidativ

Diels–Alder Polymer Networks with Temperature-Reversible Cross-Linking-Induced Emission

Hadjichristidis, Nikos,Jiang, Yu

supporting information, p. 331 - 337 (2020/12/01)

A novel synthetic strategy gives reversible cross-linked polymeric materials with tunable fluorescence properties. Dimaleimide-substituted tetraphenylethene (TPE-2MI), which is non-emissive owing to the photo-induced electron transfer (PET) between maleimide (MI) and tetraphenylethene (TPE) groups, was used to cross-link random copolymers of methyl (MM), decyl (DM) or lauryl (LM) methacrylate with furfuryl methacrylate (FM). The mixture of copolymer and TPE-2MI in DMF showed reversible fluorescence with “on/off” behavior depending on the Diels–Alder (DA)/retro-DA process, which is easily adjusted by temperature. At high temperatures, the retro-DA reaction is dominant, and the fluorescence is quenched by the photo-induced electron transfer (PET) mechanism. In contrast, at low temperatures, the emission recovers as the DA reaction takes over. A transparent PMFM/TPE-2MI polymer film was prepared which shows an accurate response to the external temperature and exhibited tunable fluorescent “turn on/off” behavior. These results suggest the possible application in areas including information security and transmission. An example of invisible/visible writing is given.

Tetraphenyl ethylene isomer having aggregation-induced emission and supramolecular polymerization properties and preparation method and application thereof

-

Paragraph 0051-0054, (2019/01/24)

The invention discloses a tetraphenyl ethylene isomer having aggregation-induced emission and supramolecular polymerization properties, and preparation method and application thereof, a chemical reaction for generating a tetraphenyl ethylene isomer is per

Room Temperature One-Step Conversion from Elemental Sulfur to Functional Polythioureas through Catalyst-Free Multicomponent Polymerizations

Tian, Tian,Hu, Rongrong,Tang, Ben Zhong

supporting information, p. 6156 - 6163 (2018/05/14)

The utilization of sulfur is a global concern, considering the abundant and cheap source of sulfur from nature and petroleum industry, its limited consumption, and the safety/environmental problems caused during storage. The economic and efficient transformation of sulfur remains to be a great challenge for both academia and industry. Herein, a room temperature conversion from sulfur to functional polythioureas was reported through a catalyst-free multicomponent polymerization of sulfur, aliphatic diamines, and diisocyanides in air with 100% atom economy. The polymerization enjoys quick reaction and wide monomer scope, which affords 16 polythioureas with well-defined structures, high molecular weights (Mws up to 242 500 g/mol), and excellent yields (up to 95%). The polythioureas can be utilized to detect mercury pollution with high sensitivity (Ksv = 224 900 L/mol) and high selectivity, clean Hg2+ with high removal efficiency (>99.99%) to achieve drinking water standard, and monitor the real-time removal process by fluorescence.

Aggregation-induced CPL response from chiral binaphthyl-based AIE-active polymers via supramolecular self-assembled helical nanowires

Ma, Jing,Wang, Yuxiang,Li, Xiaojing,Yang, Lan,Quan, Yiwu,Cheng, Yixiang

, p. 184 - 189 (2018/04/14)

In this paper chiral polymer R-P could be synthesized by click polymerization reaction of (R)-3,3′-diethynyl-2,2′-bis(octyloxy)-1,1′-binaphthalene (R-M-1) and 1,2-bis(4-azidophenyl)-1,2-diphenylethene (M-2), and S-P was obtained by click polymerization re

Insights into the general and efficient cross McMurry reactions between ketones

Duan, Xin-Fang,Zeng, Jing,Lue, Jia-Wei,Zhang, Zhan-Bin

, p. 9873 - 9876 (2007/10/03)

The selective cross McMurry couplings of diaryl or aryl ketones with various substituted ketones were achieved in 53-94% isolated yields. It is believed that the strong affinity of the substituents to the low-valent titanium surface plays an important role in regards to moderating selectivity. Through the introduction of such substituents followed by their removal post McMurry coupling, structurally similar ketones can be effectively cross-coupled.

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