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Boronic acid, B,B'-[(1,2-diphenyl-1,2-ethenediyl)di-4,1-phenylene]bis-4,4'-(1,2-Diphenyl-1,2-ethenylene)diphenylboronic acid, is a complex organic compound characterized by its boronic acid functional groups and multiple aromatic rings. This unique structure endows it with specific reactivity and properties, making it a valuable asset in the fields of chemistry and biochemistry. Its ability to form stable complexes with diols and amines highlights its importance in chemical research and development, particularly in the synthesis of medicinal compounds and the creation of advanced materials.

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  • (1,2-diphenylethene-1,2-diyl)bis(4,4'-phenylene)-1,1'-diboronic acid

    Cas No: 1054451-31-8

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  • 1054451-31-8 Structure
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    1. Product Name: Boronic acid, B,B'-[(1,2-diphenyl-1,2-ethenediyl)di-4,1-phenylene]bis- 4,4'-(1,2-Diphenyl-1,2-ethenylene)diphenylboronic acid
    2. Synonyms: Boronic acid, B,B'-[(1,2-diphenyl-1,2-ethenediyl)di-4,1-phenylene]bis- 4,4'-(1,2-Diphenyl-1,2-ethenylene)diphenylboronic acid;4,4'-(1,2-diphenylethene-1,2-diyl)bis(4,1-phenylene)diboronic acid;[(1,2-Diphenylethene-1,2-diyl)bis(4,1-phenylene)]diboronic acid
    3. CAS NO:1054451-31-8
    4. Molecular Formula:
    5. Molecular Weight: 420.08
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1054451-31-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Boronic acid, B,B'-[(1,2-diphenyl-1,2-ethenediyl)di-4,1-phenylene]bis- 4,4'-(1,2-Diphenyl-1,2-ethenylene)diphenylboronic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: Boronic acid, B,B'-[(1,2-diphenyl-1,2-ethenediyl)di-4,1-phenylene]bis- 4,4'-(1,2-Diphenyl-1,2-ethenylene)diphenylboronic acid(1054451-31-8)
    11. EPA Substance Registry System: Boronic acid, B,B'-[(1,2-diphenyl-1,2-ethenediyl)di-4,1-phenylene]bis- 4,4'-(1,2-Diphenyl-1,2-ethenylene)diphenylboronic acid(1054451-31-8)
  • 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: 1054451-31-8(Hazardous Substances Data)

1054451-31-8 Usage

Uses

Used in Organic Synthesis:
Boronic acid, B,B'-[(1,2-diphenyl-1,2-ethenediyl)di-4,1-phenylene]bis-4,4'-(1,2-Diphenyl-1,2-ethenylene)diphenylboronic acid is used as a building block in organic synthesis for the development of various medicinal compounds. Its unique structure and reactivity allow for the creation of complex organic molecules with potential therapeutic applications.
Used in Advanced Material Development:
In the field of material science, this boronic acid compound is utilized as a component in the development of advanced materials. Its ability to form stable complexes with other molecules contributes to the creation of materials with enhanced properties, such as improved stability, reactivity, or selectivity.
Used in Chemical Research:
Boronic acid, B,B'-[(1,2-diphenyl-1,2-ethenediyl)di-4,1-phenylene]bis-4,4'-(1,2-Diphenyl-1,2-ethenylene)diphenylboronic acid is employed as a valuable tool in chemical research. Its unique structure and reactivity make it an important subject of study for understanding the fundamental principles of chemical reactions and interactions, as well as for exploring new synthetic pathways and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, this boronic acid compound is used as a key intermediate in the synthesis of various drugs and drug candidates. Its ability to form stable complexes with biologically relevant molecules, such as diols and amines, makes it a promising candidate for the development of new therapeutic agents with improved efficacy and selectivity.
Used in Biochemical Research:
Boronic acid, B,B'-[(1,2-diphenyl-1,2-ethenediyl)di-4,1-phenylene]bis-4,4'-(1,2-Diphenyl-1,2-ethenylene)diphenylboronic acid is also utilized in biochemical research for studying enzyme mechanisms, protein-ligand interactions, and other biological processes. Its unique reactivity and ability to form stable complexes with biomolecules make it a valuable tool for probing and modulating biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 1054451-31-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,4,4,5 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1054451-31:
(9*1)+(8*0)+(7*5)+(6*4)+(5*4)+(4*5)+(3*1)+(2*3)+(1*1)=118
118 % 10 = 8
So 1054451-31-8 is a valid CAS Registry Number.

1054451-31-8 Well-known Company Product Price

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  • Aldrich

  • (797367)  [(1,2-Diphenylethene-1,2-diyl)bis(4,1-phenylene)]diboronic acid  

  • 1054451-31-8

  • 797367-25MG

  • 4,801.68CNY

  • Detail

1054451-31-8SDS

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 (1,2-diphenylethene-1,2-diyl)bis(4,4'-phenylene)-1,1'-diboronic acid

1.2 Other means of identification

Product number -
Other names 4,4'-(1,2-diphenylethene-1,2-diyl)bis(1,4-phenylene)diboronic acid

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:1054451-31-8 SDS

1054451-31-8Relevant articles and documents

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Page/Page column 63, (2016/04/20)

Compounds that exhibit aggregation induced emission (AIE), and more particularly to water-soluble conjugated polyene compounds that exhibit aggregation induced emission. The conjugated polyene compounds can be used as bioprobes for DNA detection, G-quadru

Incorporation of an aggregation-induced-emissive tetraphenylethene derivative into cationic gene delivery vehicles manifested the nuclear translocation of uncomplexed DNA

Han, Xiongqi,Chen, Qixian,Lu, Hongguang,Guo, Pan,Li, Wei,Wu, Guolin,Ma, Jianbiao,Gao, Hui

supporting information, p. 3907 - 3910 (2016/03/16)

A fluorophore displaying aggregation-induced emission was introduced at the terminus of branched polyethylenimine (PEI). The formulated polyplex not only demonstrated an improved safety profile and preserved transfection activity but also importantly indi

Daylight-stimulated antibacterial activity for sustainable bacterial detection and inhibition

Wu, Yuanhao,Chen, Qixian,Li, Qiaoying,Lu, Hongguang,Wu, Xinshi,Ma, Jianbiao,Gao, Hui

, p. 6350 - 6357 (2016/10/09)

Owing to the abuse of antibiotics, antibiotic resistance is spreading fast, which poses a potential threat to human beings. However, methods of the detection of bacterial viability, e.g., the plate count method, high-resolution microscopy, etc., require c

Piezochromic luminescent and electroluminescent materials comprised of tetraphenylethene plus spirobifluorene or 9,9-diphenylfluorene

He, Bairong,Chang, Zhengfeng,Jiang, Yibin,Xu, Xiaofei,Lu, Ping,Kwok, Hoi Sing,Zhou, Jian,Qiu, Huayu,Zhao, Zujin,Tang, Ben Zhong

, p. 87 - 93 (2014/04/17)

In this work, a series of luminogens comprised of tetraphenylethene plus spirobifluorene or 9,9-diphenylfluorene are synthesized and characterized. Whereas these luminogens are weakly fluorescent in solutions, they are highly emissive in the aggregated state, with high fluorescence quantum yields up to 99% in solid films, demonstrating aggregation-induced emission characteristics. Reversible piezochromic luminescence is observed from the solids of the luminogens. A notable emission color change from blue (445 nm) to green (503 nm) is readily realized by grinding the pristine powder of the luminogen. The blue emission is recovered by fuming the ground powder with dichloromethane vapor. The undoped electroluminescence devices using the luminogens as light-emitting layers are fabricated, affording high current efficiencies up to 7.2 cd/A.

AGGREGATION-INDUCED EMISSION LUMINOGENS FOR METAL ION DETECTION

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, (2013/03/26)

Pyridine-containing polyenes and their applications as metal ion sensors. These polyenes are practically nonluminescent in the solution state but become highly emissive as nanoparticle suspensions in aqueous solutions or thin films in the solid state, due

Luminogenic materials constructed from tetraphenylethene building blocks: Synthesis, aggregation-induced emission, two-photon absorption, light refraction, and explosive detection

Hu, Rongrong,Maldonado, Jose Luis,Rodriguez, Mario,Deng, Chunmei,Jim, Cathy K. W.,Lam, Jacky W. Y.,Yuen, Matthew M. F.,Ramos-Ortiz, Gabriel,Tang, Ben Zhong

, p. 232 - 240 (2013/01/12)

Luminogenic molecules [(TPE)3 (1), TPE-C = C-TPE-C = C-TPE (2), and TPE-C≡C-TPE-C≡C-TPE (3)] and their polymers P1-P3 are constructed from tetraphenylethene (TPE) building blocks in high yields by Suzuki, Witting, and Sonogashira coupling react

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