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1155-51-7

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1155-51-7 Usage

Description

4,4'-Dithiobisbenzoic Acid, Technical Grade (CAS# 1155-51-7) is a pale yellow crystalline powder that serves as a versatile compound in the realm of organic synthesis. Its unique chemical structure allows for a wide range of applications across different industries, making it a valuable asset in the field of chemistry.

Uses

Used in Organic Synthesis:
4,4'-Dithiobisbenzoic Acid, Technical Grade is used as a synthetic building block for the creation of various organic compounds. Its chemical properties enable it to be a key component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4,4'-Dithiobisbenzoic Acid, Technical Grade is used as an intermediate in the development of new drugs. Its unique structure allows for the creation of novel therapeutic agents that can target specific biological pathways, potentially leading to more effective treatments for various diseases.
Used in Analytical Chemistry:
4,4'-Dithiobisbenzoic Acid, Technical Grade is utilized as a reagent in analytical chemistry for the detection and quantification of various substances. Its ability to form complexes with certain compounds makes it a valuable tool in the identification and measurement of specific analytes.
Used in Material Science:
In the field of material science, 4,4'-Dithiobisbenzoic Acid, Technical Grade is employed in the development of new materials with unique properties. Its incorporation into polymers and other materials can lead to enhanced performance characteristics, such as improved stability, strength, or conductivity.
Used in Research and Development:
4,4'-Dithiobisbenzoic Acid, Technical Grade is also used as a research compound in academic and industrial laboratories. Its diverse applications make it an essential tool for scientists and researchers working on the development of new technologies and products.

Check Digit Verification of cas no

The CAS Registry Mumber 1155-51-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,5 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1155-51:
(6*1)+(5*1)+(4*5)+(3*5)+(2*5)+(1*1)=57
57 % 10 = 7
So 1155-51-7 is a valid CAS Registry Number.

1155-51-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 4,4'-Dithiobenzoic 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:1155-51-7 SDS

1155-51-7Relevant articles and documents

Practical and efficient recyclable oxidative system for the preparation of symmetrical disulfides under aerobic conditions

Ling, Ong Chiu,Heidelberg, Thorsten,Ching, Juan Joon,Khaligh, Nader Ghaffari

, p. 281 - 294 (2021)

An efficient and practical oxidative coupling of thiols to symmetrical disulfides is developed at room temperature under aerobic conditions. The commercially available sodium methoxide solution 30 wt. % in methanol together with the air was used as a retrievable promoter system and green oxidant, respectively, for the preparation of symmetrical disulfides. The desired products were obtained in good to high yields by an economical procedure. No overoxidation of the symmetrical disulfides was observed, and various functional groups were well tolerated in the current protocol. Moreover, the new reagent reduces the generation of hazardous waste due to its high reusability. The reaction proceeded in the absence of light, and it was not inhibited by TEMPO. Also, the low yield of TEMPO-benzyl thiol adduct was detected under these conditions. Based on our experiments, a possible mechanism was proposed in the absence and presence of TEMPO.

Bifunctional Chalcogen Linkers for the Stepwise Generation of Multimetallic Assemblies and Functionalized Nanoparticles

Robson, Jonathan A.,Gonzàlez De Rivera, Ferran,Jantan, Khairil A.,Wenzel, Margot N.,White, Andrew J. P.,Rossell, Oriol,Wilton-Ely, James D. E. T.

, p. 12982 - 12996 (2016)

The disulfide ligand (SC6H4CO2H-4)2 acts as a simple but versatile linker for a range of group 8 transition metals through reaction of the oxygen donors. This leads to a range of homobimetallic ruthenium and osm

Enzymatic thiol Michael addition using laccases: Multiple C-S bond formation between p-hydroquinones and aromatic thiols

Schlippert, Max,Mikolasch, Annett,Hahn, Veronika,Schauer, Frieder

, p. 106 - 114 (2016)

Laccases create C-C, C-O or C-N bonds and have been investigated intensively as catalysts for green chemistry and white biotechnology. However, little is known about C-S bond formation in laccase-catalyzed reactions. We have used the laccases from Pycnopo

Highly sensitive SERS quantification of the oncogenic protein c-Jun in cellular extracts

Guerrini, Luca,Pazos, Elena,Penas, Cristina,Vazquez, M. Eugenio,Mascarenas, Jose Luis,Alvarez-Puebla, Ramon A.

, p. 10314 - 10317 (2013)

A surface-enhanced Raman scattering (SERS)-based sensor was developed for the detection of the oncoprotein c-Jun at nanomolar levels. c-Jun is a member of the bZIP (basic zipper) family of dimeric transcriptional activators, and its overexpression has bee

Solid phase synthesis of bicyclic pyrrolidines

Quadrelli, Paolo

, (2021/11/17)

The preparation of bicyclic pyrrolidines, stable and easy to isolate, is performed through both classical solution chemistry and on solid support. A new linker strategy is presented based on the concept of REM resin approach. Starting from a suitably derivatized Wang's resin, the linker can be REgenerated after cleavage of the product and functionalized to start a new synthetic cycle via a Michael reaction. In the present work a vinyl sulfone supported on a Wang's resin is able to undergo a Michael reaction with an amino acid derivative; the obtained adduct serves as a precursor for azomethine ylide generation, which is conveniently trapped with N-methyl-maleimide. The results are presented and discussed in the light of the experimental conditions applied as well as the method chosen for the cleavage of the product and resin regeneration.

Silane, rubber mixture containing the silane and vehicle tyre having the rubber mixture in at least one component

-

Page/Page column 15-16, (2020/12/21)

The invention relates to a silane, to a rubber mixture comprising the silane and to a vehicle tire comprising the rubber mixture in at least one component. The inventive silane has the following formula I) [in-line-formulae](R1)oSi—R2—X-A-Y-[A-Y-]m-A-Sk-A-[-Y-A]mY-A-X—R2—Si(R1)o,[/in-line-formulae] wherein, according to the invention, the silane has spacer groups between the respective silyl groups and the Sk moiety which have at least two aromatic groups A and the linking units X and Y, wherein the groups X within a molecule may be identical or different from each other and are selected from the groups —HNC(═O)—, —C(═O)NH—, —C(═O)O—, —OC(═O)—, —OC(═O)NH—, —HNC(═O)O—, —R3NC(═O)NR3—, —R3NC(═NR3)NR3—, —R3NC(═S)NR3—, wherein at least one R3 within each group X is a hydrogen atom; and wherein the groups Y within a molecule may be identical or different from each other and are selected from the groups —HNC(═O)—, —C(═O)NH—, —C(═O)O—, —OC(═O)—, —OC(═O)NH—,—HNC(═O)O—, —R4NC(═O)NR4—, —R4NC(═NR4)NR4—, —R4NC(═S)NR4—, wherein at least one R4 within each group Y is a hydrogen atom. The inventive rubber mixture comprises at least one inventive silane.

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