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Benzoic acid, 4,4'-(dimethylsilylene)bis-, also known as bis(4-hydroxyphenyl)dimethylsilane, is a chemical compound characterized by a benzene ring with a carboxylic acid functional group and two silicon atoms connected to the benzene ring via dimethylsilylene bridges. Benzoic acid,4,4'-(dimethylsilylene)bisexhibits antimicrobial properties and is soluble in organic solvents with low solubility in water.

17003-01-9

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17003-01-9 Usage

Uses

Used in Food and Beverage Industry:
Benzoic acid, 4,4'-(dimethylsilylene)bisis used as a preservative for its antimicrobial properties, helping to extend the shelf life of various food and beverage products by inhibiting the growth of bacteria, yeasts, and molds.
Used in Plastics Industry:
Benzoic acid,4,4'-(dimethylsilylene)bisis utilized in the production of plastics due to its ability to enhance the stability and durability of the materials, making them more resistant to degradation from environmental factors.
Used in Dyes Industry:
Benzoic acid, 4,4'-(dimethylsilylene)bisis employed in the manufacturing of dyes, where it contributes to the color stability and performance of the dyes in various applications, such as textiles, paints, and inks.
Used in Perfumery:
In the perfume industry, Benzoic acid,4,4'-(dimethylsilylene)bis- is used as a fixative agent to help extend the longevity of fragrances, ensuring that the scent remains consistent and long-lasting on various surfaces.
Used in Organic Synthesis:
Benzoic acid, 4,4'-(dimethylsilylene)bisserves as a valuable intermediate in organic synthesis, particularly in the preparation of various pharmaceuticals, agrochemicals, and other specialty chemicals, due to its unique structural features and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 17003-01-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,0 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17003-01:
(7*1)+(6*7)+(5*0)+(4*0)+(3*3)+(2*0)+(1*1)=59
59 % 10 = 9
So 17003-01-9 is a valid CAS Registry Number.

17003-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(4-carboxyphenyl)-dimethylsilyl]benzoic acid

1.2 Other means of identification

Product number -
Other names 4,4'-Dimethylsilandiyl-di-benzoesaeure

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:17003-01-9 SDS

17003-01-9Relevant academic research and scientific papers

Synthesis, photophysical and electrochemical properties of symmetric silicon-linked coumarin-oxadiazole derivatives

Zhang, Lingling,Xia, Yan,Li, Min,Li, Dongfeng,Hou, Ruibin

, p. 7438 - 7442 (2016)

A novel, silicon-linked, symmetric, V-shaped, coumarin derivative (1) with an electron-deficient 1,3,4-oxadiazoles unit and a phenyl moiety was synthesized and characterized. An efficient multifunctional organic light-emitting diode material was obtained

Design, synthesis, and photoelectric properties of v-shaped organic fluorescent compounds with a 1,3,4-oxadiazole moiety

Hou, Rui-Bin,Su, Ji-Ying,Zhang, Ling-Ling,Li, Dong-Feng,Xia, Yan

, p. 3 - 7 (2019/06/03)

A series of symmetric, silicon-linked organic fluorescent compounds with two electron-deficient 1,3,4-oxadiazole units were synthesized and characterized. The compounds possessed a V-shaped structure with a silicon atom, which weakened π–π stacking, promoting aggregation-induced emission. The compounds were fluorescent in both solution and solid-state thin films. The efficient fluorescent behavior of the materials was confirmed through optical and electrochemical measurements. The compounds displayed excellent thermal stability, with decomposition temperatures exceeding 400 °C. Amorphous films of the compounds possessed high morphological stability. These results indicate that the compounds may be promising emissive and electron-transporting materials.

Electronic alteration of end-on phenyl groups of bis-triazolyl-silanes: Electron-transport materials for blue phosphorescent OLEDs

Yi, Seungjun,Bae, Woo-Ri,Kim, Jin-Hyoung,Lee, Ah-Rang,Kim, Woo-Young,Han, Won-Sik,Son, Ho-Jin,Kang, Sang Ook

, p. 4978 - 4987 (2016/06/15)

A series of modified bis(4-(4,5-diphenyl-4H-1,2,4-triazol-3-yl)phenyl)dimethylsilane (ST), ST-CF3, ST-Me, ST-tBu, and ST-OMe, were designed and prepared by introducing electron-withdrawing groups or electron-donating groups at the 4-

Silicon-containing aromatic poly(esters) derived from bis(4-carboxyphenyl) methyl-r-silane and bis(4-(hydroxymethyl) phenyl)methyl-r-silane. synthesis, characterization and thermal studies

Tagle, Luis H.,Terraza, Claudio A.,Pino, Leonardo I.

, p. 1166 - 1169,4 (2020/08/24)

This work describes the synthesis, characterization and thermal studies of poly(esters) (PEs) containing two Si atoms in the main chain, derived from aromatic diacids and aliphatic dialcohols in which the Si atom is bonded to methyl and/or ethyl groups. P

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