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13698-87-8

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13698-87-8 Usage

General Description

N,N'-tetraethylisophthalamide is a chemical compound commonly used as a corrosion inhibitor and an additive in various industrial processes. It is a colorless to pale yellow liquid with a faint odor, and it is soluble in organic solvents. NNN'N'-TETRAETHYLISOPHTHALAMIDE is often added to metalworking fluids to protect machinery and parts from corrosion, as well as to improve the lubricating and cooling properties of the fluid. N,N'-tetraethylisophthalamide is also used as an intermediate in the production of pharmaceuticals, dyes, and polymers. It is known to be relatively stable and non-reactive under normal conditions, making it a versatile and valuable chemical in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 13698-87-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,9 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13698-87:
(7*1)+(6*3)+(5*6)+(4*9)+(3*8)+(2*8)+(1*7)=138
138 % 10 = 8
So 13698-87-8 is a valid CAS Registry Number.

13698-87-8SDS

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 1-N,1-N,3-N,3-N-tetraethylbenzene-1,3-dicarboxamide

1.2 Other means of identification

Product number -
Other names 1,3-Benzenedicarboxamide, N,N,N‘,N‘-tetraethyl-

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:13698-87-8 SDS

13698-87-8Relevant articles and documents

One-Pot Synthesis of Tertiary Amides from Organic Trichlorides through Oxygen Atom Incorporation from Air by Convergent Paired Electrolysis

Luo, Zhongli,Imamura, Kenji,Shiota, Yoshihito,Yoshizawa, Kazunari,Hisaeda, Yoshio,Shimakoshi, Hisashi

, p. 5983 - 5990 (2021/05/04)

A convergent paired electrolysis catalyzed by a B12 complex for the one-pot synthesis of a tertiary amide from organic trichlorides (R-CCl3) has been developed. Various readily available organic trichlorides, such as benzotrichloride and its derivatives, chloroform, dichlorodiphenyltrichloroethane (DDT), trichloro-2,2,2-trifluoroethane (CFC-113a), and trichloroacetonitrile (CNCCl3), were converted to amides in the presence of tertiary amines through oxygen incorporation from air at room temperature. The amide formation mechanism in the paired electrolysis, which was mediated by a cobalt complex, was proposed.

Visible Light-Driven, One-pot Amide Synthesis Catalyzed by the B12 Model Complex under Aerobic Conditions

Tian, Hui,Shimakoshi, Hisashi,Ono, Toshikazu,Hisaeda, Yoshio

, p. 237 - 240 (2018/12/13)

A visible light responsive catalytic system with the B12 complex as the catalyst and [Ir(dtbbpy)(ppy)2]PF6 as the photosensitizer was developed. It provides a convenient and efficient way to synthesize amides. Based on this method, trichlorinated organic compounds were converted into amides in the presence of an amine under aerobic conditions at room temperature in a one-pot procedure. Various trichlorinated organic compounds and an amine source, such as primary, secondary, and cyclic amines, have been evaluated for this transformation, providing the expected products in moderate to excellent yields. Notably, product formation depended on the reaction atmosphere where the amide was obtained under aerobic conditions while partially dechlorinated products were obtained under anaerobic conditions. As this protocol is free from hazardous reagents, extra additives, noble metals, and dangerous gas, the present method provides a novel and efficient approach for amide synthesis under mild and easily controlled conditions.

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