161768-66-7 Usage
Uses
Used in Pharmaceutical Industry:
4-Bromo-N-isobutylbenzamide is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs and medicinal compounds.
Used in Organic Chemistry Research:
In the field of organic chemistry, 4-Bromo-N-isobutylbenzamide is utilized as a research compound to study its properties, reactions, and potential applications. It aids chemists in understanding the behavior of benzamides and their derivatives, contributing to the advancement of organic chemistry knowledge.
Used in Laboratory Settings:
4-Bromo-N-isobutylbenzamide is employed in laboratories for various experimental purposes, such as testing its reactivity, stability, and potential interactions with other compounds. This helps researchers to explore its potential uses and develop new methods for its synthesis and application.
Used in Chemical Synthesis:
As a chemical intermediate, 4-Bromo-N-isobutylbenzamide is used in the synthesis of other organic compounds. Its unique structure allows it to participate in various chemical reactions, enabling the creation of new molecules with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 161768-66-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,7,6 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 161768-66:
(8*1)+(7*6)+(6*1)+(5*7)+(4*6)+(3*8)+(2*6)+(1*6)=157
157 % 10 = 7
So 161768-66-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H14BrNO/c1-8(2)7-13-11(14)9-3-5-10(12)6-4-9/h3-6,8H,7H2,1-2H3,(H,13,14)
161768-66-7Relevant articles and documents
Amidation and esterification of carboxylic acids with amines and phenols by N,N′-diisopropylcarbodiimide: A new approach for amide and ester bond formation in water
Fattahi, Nadia,Ayubi, Morteza,Ramazani, Ali
, p. 4351 - 4356 (2018/07/13)
The present study reports the successful synthesis of two important and abundant functional groups “ester and amide” by N,N′-diisopropylcarbodiimide (DIC) in water as a green solvent. A wide range of substrates could be employed with high functional group tolerance. The products were obtained in high yields after short reaction times. This method provides an efficient, economic, simple and very mild protocol for ester and amide bond formation in aqueous media. In addition, this work not only may lead to environmentally benign systems but also will provide a new aspect of organic chemistry in water.
In Situ Oxidation-Imine Formation-Reduction Routes from Alcohols to Amines
Blackburn, Leonie,Taylor, Richard J. K.
, p. 1637 - 1639 (2007/10/03)
(matrix presented) Manganese dioxide is employed as an in situ oxidant for the one-pot conversion of alcohols into imines. In combination with polymer-supported cyanoborohydride (PSCBH), a one-pot oxidation-imine formation-reduction sequence is reported. This procedure enables alcohols to be converted directly into both secondary and tertiary amines.
