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1046045-61-7

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1046045-61-7 Usage

Description

FGH-10019 is a chemical compound that belongs to the class of cyanoacrylate adhesives, commonly referred to as superglue. It is characterized by its fast-setting nature and high strength, making it an ideal choice for bonding a diverse array of materials such as plastics, metals, and rubber. The adhesive is renowned for its rapid curing properties and the formation of a durable bond that is resistant to heat, moisture, and chemicals, which renders it suitable for various industrial and commercial applications.

Uses

Used in General Adhesive Applications:
FGH-10019 is used as a fast-setting adhesive for its ability to quickly bond a wide range of materials, providing high strength and durability in the resulting bond.
Used in Industrial Settings:
In the industrial sector, FGH-10019 is used as a high-strength adhesive for bonding components that require resistance to heat, moisture, and chemicals, ensuring the longevity and reliability of the products manufactured.
Used in Commercial Settings:
FGH-10019 serves as a versatile adhesive in commercial applications, where its rapid curing and strong bonding capabilities are essential for quick repairs and maintenance tasks, contributing to operational efficiency.
Used in Plastics Industry:
FGH-10019 is used as a bonding agent in the plastics industry for joining plastic components, leveraging its compatibility with various types of plastics and its ability to form strong bonds.
Used in Metalworking:
FGH-10019 is utilized as an adhesive in metalworking for securing metal parts, taking advantage of its high-strength bonding properties and resistance to environmental factors.
Used in Rubber Industry:
In the rubber industry, FGH-10019 is employed as an adhesive for bonding rubber materials, capitalizing on its capacity to create durable and flexible bonds that can withstand various conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1046045-61-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,6,0,4 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1046045-61:
(9*1)+(8*0)+(7*4)+(6*6)+(5*0)+(4*4)+(3*5)+(2*6)+(1*1)=117
117 % 10 = 7
So 1046045-61-7 is a valid CAS Registry Number.

1046045-61-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name FGH10019

1.2 Other means of identification

Product number -
Other names N-(4-(2-(2-propylpyridin-4-yl)thiazol-4-yl)phenyl)methanesulfonamide

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:1046045-61-7 SDS

1046045-61-7Downstream Products

1046045-61-7Relevant articles and documents

SYNTHESIS OF FATOSTATIN BASED POLYCYCLIC COMPOUNDS

-

, (2016/06/01)

The present invention relates to methods and strategies for large-scale synthesis of compounds having the chemical structure: (I). The R substituents are H, methyl, isopropyl, benzyl, cyclohexyl, cyclopropylmethyl, methoxy, tert-butyloxycarbonyl, methanes

Synthesis and evaluation of diarylthiazole derivatives that inhibit activation of sterol regulatory element-binding proteins

Kamisuki, Shinji,Shirakawa, Takashi,Kugimiya, Akira,Abu-Elheiga, Lutfi,Park Choo, Hea-Young,Yamada, Kohei,Shimogawa, Hiroki,Wakil, Salih J.,Uesugi, Motonari

experimental part, p. 4923 - 4927 (2011/09/19)

Fatostatin, a recently discovered small molecule that inhibits activation of sterol regulatory element-binding protein (SREBP), blocks biosynthesis and accumulation of fat in obese mice. We synthesized and evaluated a series of fatostatin derivatives. Our

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