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1077-56-1

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1077-56-1 Usage

General Description

N-Ethyl-o-toluenesulfonamide is a chemical compound with the molecular formula C9H11NO2S. It is used primarily as a plasticizer and as an additive in various industrial and consumer products, such as adhesives, coatings, and polymers. It is also commonly used as an anti-corrosion agent in metalworking fluids. N-Ethyl-o-toluenesulfonamide is known for its low volatility and excellent thermal stability, making it suitable for use in high-temperature applications. However, it is important to handle this chemical with care as it can be harmful if ingested or inhaled, and can cause irritation to the skin and eyes. Therefore, proper safety precautions and handling procedures should be followed when working with N-Ethyl-o-toluenesulfonamide.

Check Digit Verification of cas no

The CAS Registry Mumber 1077-56-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1077-56:
(6*1)+(5*0)+(4*7)+(3*7)+(2*5)+(1*6)=71
71 % 10 = 1
So 1077-56-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO2S/c1-3-10-13(11,12)9-7-5-4-6-8(9)2/h4-7,10H,3H2,1-2H3

1077-56-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Ethyl-o-toluenesulfonamide

1.2 Other means of identification

Product number -
Other names o-N-Ethyltoluene sulfonamide

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:1077-56-1 SDS

1077-56-1Relevant articles and documents

Copper-catalyzed trifluoromethylation and cyclization of aromatic-sulfonyl-group-tethered alkenes for the construction of 1,2-benzothiazinane dioxide type compounds

Dong, Xiang,Sang, Rui,Wang, Qiang,Tang, Xiang-Ying,Shi, Min

, p. 16910 - 16915 (2013)

A multi-talented system: An efficient copper-catalyzed tandem trifluoromethylation/annulation of an electron-deficient aromatic ring has been developed. This method provides a powerful and straightforward way to synthesize trifluoromethylated 1,2-benzothiazinane dioxides under mild conditions (see scheme). The mechanism was investigated by a series of kinetic experiments and isotopic labeling studies.

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