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t-Butyl 4-carboxybenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

215118-68-6

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215118-68-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 215118-68-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,1,1 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 215118-68:
(8*2)+(7*1)+(6*5)+(5*1)+(4*1)+(3*8)+(2*6)+(1*8)=106
106 % 10 = 6
So 215118-68-6 is a valid CAS Registry Number.

215118-68-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(tert-butylcarbamoyl)benzoic acid

1.2 Other means of identification

Product number -
Other names N-tert-butylterephthalamic acid

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:215118-68-6 SDS

215118-68-6Downstream Products

215118-68-6Relevant academic research and scientific papers

High-efficiency aminocarbonylation by introducing CO to a pressurized continuous flow reactor

Csajgi, Csaba,Borcsek, Bernadett,Niesz, Krisztin,Kovcs, Ildik,Szkelyhidi, Zsolt,Bajk, Zoltn,Rge, Lszl,Darvas, Ferenc

supporting information; experimental part, p. 1589 - 1592 (2009/04/07)

Halogenated aryl carboxylic acids were efficiently converted to the corresponding dicarboxylic acid monoamides by a one-step Pd-catalyzed aminocarbonylation in a micro/meso fluidic continuous flow reactor (X-Cube) operated at high pressure and high temperature with CO gas introduction. Reaction parameters (solvent, base, catalyst, pressure, temperature) were rapidly optimized in the reactions, which required less than 2 min. The method gave improved results over comparable batch techniques and is also suited to automated parallel syntheses of compound libraries.

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