98276-91-6 Usage
Description
CHEMBRDG-BB 4009838, also known as 3-(2-aminoethylamino)propylmethyldimethoxysilane, is a versatile chemical compound that serves as a coupling agent and adhesion promoter in various industrial applications. It is particularly effective in enhancing the bonding of organic materials to inorganic surfaces such as glass, metal, and other materials. The presence of amino and methoxy functional groups makes it suitable for use as a surface modifier and treatment agent. Furthermore, CHEMBRDG-BB 4009838 is known for its ability to improve the stability, durability, and performance of composite materials.
Uses
Used in Adhesives and Sealants Industry:
CHEMBRDG-BB 4009838 is used as a coupling agent and adhesion promoter for improving the bonding strength between organic and inorganic materials in the production of adhesives and sealants. Its ability to enhance the interfacial adhesion contributes to the development of high-performance adhesives and sealants with increased durability and stability.
Used in Coatings Industry:
In the coatings industry, CHEMBRDG-BB 4009838 is utilized as a surface modifier and treatment agent to improve the adhesion, durability, and performance of coatings applied on various substrates. Its presence in the coating formulation helps in achieving better adhesion to the substrate, resulting in coatings with enhanced resistance to wear, corrosion, and environmental factors.
Used in Composite Materials Industry:
CHEMBRDG-BB 4009838 is employed as a coupling agent in the production of composite materials to improve the interfacial bonding between the organic and inorganic components. This enhanced bonding contributes to the overall stability, durability, and performance of the composite materials, making them suitable for various applications in industries such as aerospace, automotive, and construction.
Check Digit Verification of cas no
The CAS Registry Mumber 98276-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,2,7 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 98276-91:
(7*9)+(6*8)+(5*2)+(4*7)+(3*6)+(2*9)+(1*1)=186
186 % 10 = 6
So 98276-91-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O3S/c1-4-2-5(10)9-7(8-4)13-3-6(11)12/h2H,3H2,1H3,(H,11,12)(H,8,9,10)
98276-91-6Relevant articles and documents
Novel Aryl-Substituted Pyrimidones as Inhibitors of 3-Mercaptopyruvate Sulfurtransferase with Antiproliferative Efficacy in Colon Cancer
Bantzi, Marina,Augsburger, Fiona,Loup, Jérémie,Berset, Yan,Vasilakaki, Sofia,Myrianthopoulos, Vassilios,Mikros, Emmanuel,Szabo, Csaba,Bochet, Christian G.
, p. 6221 - 6240 (2021/05/06)
The enzyme 3-mercaptopyruvate sulfurtransferase (3-MST) is one of the more recently identified mammalian sources of H2S. A recent study identified several novel 3-MST inhibitors with micromolar potency. Among those, (2-[(4-hydroxy-6-methylpyrimidin-2-yl)sulfanyl]-1-(naphthalen-1-yl)ethan-1-one) or HMPSNE was found to be the most potent and selective. We now took the central core of this compound and modified the pyrimidone and the arylketone sides independently. A 63-compound library was synthesized; compounds were tested for H2S generation from recombinant 3-MST in vitro. Active compounds were subsequently tested to elucidate their potency and selectivity. Computer modeling studies have delineated some of the key structural features necessary for binding to the 3-MST's active site. Six novel 3-MST inhibitors were tested in cell-based assays: they exerted inhibitory effects in murine MC38 and CT26 colon cancer cell proliferation; the antiproliferative effect of the compound with the highest potency and best cell-based activity (1b) was also confirmed on the growth of MC38 tumors in mice.
Formation of Mesoionic Thiazolopyrimidines from 2-Thiouracil Derivatives
Talukdar, P. B.,Sengupta, S. K.,Datta, A. K.
, p. 275 - 278 (2007/10/02)
Carboxymethylthio derivatives (III, R2= H, Ph) from some 2-thiouracil derivatives (I) show considerable variation in their solubility behaviour in water and stability towards various reagents.Cyclodehydration of III (R2 = Ph) and VII
