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2,6-BIS(1-METHYLETHYL)PHENOXYSULFONYLISOCYANATE, also known as bis(isocyanatomethyl)benzene, is a chemical compound characterized by its molecular formula C15H19NO4S. It is a sulfonate aromatic isocyanate, recognized for its capacity to form rigid and durable polymers. This property makes it a valuable component in the manufacturing of various products, including polyurethane foam, coatings, adhesives, and sealants, and it is widely utilized across different industries for its performance-enhancing characteristics.

73748-46-6

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73748-46-6 Usage

Uses

Used in the Polyurethane Industry:
2,6-BIS(1-METHYLETHYL)PHENOXYSULFONYLISOCYANATE is used as a key ingredient in the production of polyurethane foam for its ability to create a rigid structure that offers excellent support and durability. This makes it suitable for applications such as furniture cushioning, insulation materials, and automotive components.
Used in the Coatings Industry:
In the coatings industry, 2,6-BIS(1-METHYLETHYL)PHENOXYSULFONYLISOCYANATE is used as a component in formulating coatings that require high durability and resistance to wear. Its contribution to the formation of strong polymers enhances the protective qualities of the coatings, making them ideal for use in industrial settings where surfaces need to withstand harsh conditions.
Used in the Adhesives Industry:
As a component in adhesive formulations, 2,6-BIS(1-METHYLETHYL)PHENOXYSULFONYLISOCYANATE is used for its capacity to create strong bonds between various substrates. The resulting adhesives are known for their high strength and resistance to environmental factors, making them suitable for applications in construction, automotive, and manufacturing sectors.
Used in the Sealants Industry:
In sealant production, 2,6-BIS(1-METHYLETHYL)PHENOXYSULFONYLISOCYANATE is utilized to enhance the sealing properties of the products. The sealants made with 2,6-BIS(1-METHYLETHYL)PHENOXYSULFONYLISOCYANATE are effective in preventing the passage of air, water, and other substances through joints and seams, providing a reliable solution for sealing in construction and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 73748-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,4 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73748-46:
(7*7)+(6*3)+(5*7)+(4*4)+(3*8)+(2*4)+(1*6)=156
156 % 10 = 6
So 73748-46-6 is a valid CAS Registry Number.

73748-46-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [2,6-di(propan-2-yl)phenyl] N-(oxomethylidene)sulfamate

1.2 Other means of identification

Product number -
Other names (2,6-bis(1-methylethyl)phenoxy)sulfonyl isocyanate

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:73748-46-6 SDS

73748-46-6Relevant academic research and scientific papers

Inhibitors of acyl-CoA:Cholesterol O-acyltransferase. 17. Structure-activity relationships of several series of compounds derived from N-chlorosulfonyl isocyanate

Picard, Joseph A.,O'Brien, Patrick M.,Sliskovic, Drago R.,Anderson, Maureen K.,Bousley, Richard F.,Hamelehle, Katherine L.,Krause, Brian R.,Stanfield, Richard L.

, p. 1243 - 1252 (2007/10/03)

Several series of acyl-CoA:cholesterol O-acyltransferase inhibitors were prepared by the stepwise addition of nitrogen, oxygen, and sulfur nucleophiles to N-chlorosulfonyl isocyanate. The (aminosulfonyl)ureas 3-44 were the most potent inhibitors in vitro,

SYNTHESES A L'AIDE D'HETEROCUMULENES. 4. Action L'Isocyanate De Chlorosulfonyle Sur les Phenols Encombres

Hedayatullah, Mir,Hugueny, Jean Claude

, p. 167 - 172 (2007/10/02)

The synthesis of the N-chlorosulfonylcarbamates derived from seven hindered phenols is described, as well as their hydrolysis giving a high yield of the corresponding simple carbamates, the selective substitution of their chlorine atom by the anilino radi

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