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1315329-43-1

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1315329-43-1 Usage

Description

HG6-64-1 is a halogenated organic compound primarily used as a flame retardant in various materials due to its high efficiency in preventing the spread of fire. It is known for its stability and effectiveness in reducing the flammability of materials, making it a widely utilized flame retardant in the industry.

Uses

Used in Textile Industry:
HG6-64-1 is used as a flame retardant in textiles to improve their fire resistance and safety, ensuring compliance with fire safety regulations and standards.
Used in Plastics Industry:
HG6-64-1 is used as a flame retardant in the manufacturing of plastics to enhance their fire resistance, providing safety and meeting industry-specific fire safety requirements.
Used in Other Industries:
HG6-64-1 is used as a flame retardant in various other materials and applications to reduce flammability, improve fire safety, and meet fire safety regulations and standards in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1315329-43-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,3,2 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1315329-43:
(9*1)+(8*3)+(7*1)+(6*5)+(5*3)+(4*2)+(3*9)+(2*4)+(1*3)=131
131 % 10 = 1
So 1315329-43-1 is a valid CAS Registry Number.

1315329-43-1Downstream Products

1315329-43-1Relevant articles and documents

Discovery of type II inhibitors of tgfβ-activated kinase 1 (TAK1) and mitogen-activated protein kinase kinase kinase kinase 2 (MAP4K2)

Tan, Li,Nomanbhoy, Tyzoon,Gurbani, Deepak,Patricelli, Matthew,Hunter, John,Geng, Jiefei,Herhaus, Lina,Zhang, Jianming,Pauls, Eduardo,Ham, Youngjin,Choi, Hwan Geun,Xie, Ting,Deng, Xianming,Buhrlage, Sara J.,Sim, Taebo,Cohen, Philip,Sapkota, Gopal,Westover, Kenneth D.,Gray, Nathanael S.

, p. 183 - 196 (2015/03/04)

We developed a pharmacophore model for type II inhibitors that was used to guide the construction of a library of kinase inhibitors. Kinome-wide selectivity profiling of the library resulted in the identification of a series of 4-substituted 1H-pyrrolo[2,

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