79839-66-0 Usage
Description
2-Bromo-N,N-diisopropylbenzamide, commonly referred to as BDI, is a versatile chemical compound characterized by its white to off-white crystalline appearance. It serves as a crucial intermediate in the synthesis of a range of pharmaceuticals and agrochemicals. With a molecular formula of C15H22BrNO and a molecular weight of 312.25 g/mol, BDI is recognized for its role as a building block in the creation of antihypertensive and anti-inflammatory medications, as well as in the development of herbicides and insecticides.
Uses
Used in Pharmaceutical Industry:
2-Bromo-N,N-diisopropylbenzamide is used as a key intermediate for the synthesis of various pharmaceuticals, specifically for the production of antihypertensive and anti-inflammatory drugs. Its chemical structure allows for the development of medications that can effectively manage blood pressure and reduce inflammation.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Bromo-N,N-diisopropylbenzamide is utilized as a precursor in the formulation of herbicides and insecticides. Its incorporation aids in the creation of products that protect crops from pests and unwanted plant species, thereby ensuring increased agricultural productivity.
Safety Precautions:
It is imperative to handle 2-Bromo-N,N-diisopropylbenzamide with care due to its potential to cause skin and eye irritation. To mitigate such risks, it should be used in well-ventilated areas, and individuals working with BDI must employ appropriate protective equipment.
Check Digit Verification of cas no
The CAS Registry Mumber 79839-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,3 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79839-66:
(7*7)+(6*9)+(5*8)+(4*3)+(3*9)+(2*6)+(1*6)=200
200 % 10 = 0
So 79839-66-0 is a valid CAS Registry Number.
79839-66-0Relevant articles and documents
Identification of key functionalization species in the Cp?Ir(iii)-catalyzed-: ortho halogenation of benzamides
Brown, Caleb A.,Guzmán Santiago, Alexis J.,Ison, Elon A.,Sommer, Roger D.
, p. 16166 - 16174 (2020/12/03)
Cp?Ir(iii) complexes have been shown to be effective for the halogenation of N,N-diisopropylbenzamides with N-halosuccinimide as a suitable halogen source. The optimized conditions for the iodination reaction consist of 0.5 mol% [Cp?IrCl2]2 in 1,2-dichlor
Amide Effects in C?H Activation: Noncovalent Interactions with L-Shaped Ligand for meta Borylation of Aromatic Amides
Bisht, Ranjana,Hoque, Md Emdadul,Chattopadhyay, Buddhadeb
, p. 15762 - 15766 (2018/11/10)
A new concept for the meta-selective borylation of aromatic amides is described. It has been demonstrated that while esters gave para borylations, amides lead to meta borylations. For achieving high meta selectivity, an L-shaped bifunctional ligand has been employed and engages in an O???K noncovalent interaction with the oxygen atom of the moderately distorted amide carbonyl group. This interaction provides exceptional control for meta C?H activation/borylation.
Ruthenium-catalyzed ortho-C-H halogenations of benzamides
Wang, Lianhui,Ackermann, Lutz
, p. 1083 - 1085 (2014/01/17)
[Ru3(CO)12] and AgO2C(1-Ad) enabled the first ruthenium-catalyzed intermolecular halogenations of arenes via C-H activation. Thereby, brominations and iodinations of electron-rich and electron-deficient benzamides were ach
