2315-86-8 Usage
Description
3-Bromo-4-hydroxybenzonitrile, also known as 3-Bromo-4-cyanophenol, is an organic compound characterized by its brown crystalline or needle-like appearance. It is a derivative of benzonitrile, featuring a bromine atom at the 3rd position and a hydroxyl group at the 4th position of the benzene ring.
Uses
Used in Pharmaceutical Industry:
3-Bromo-4-hydroxybenzonitrile is used as a reactant for the synthesis of various tetrazoles, which are important in the development of pharmaceutical compounds. Tetrazoles have a wide range of applications in the medical field, including their use as anti-inflammatory, antifungal, and antimicrobial agents.
Used in Chemical Synthesis:
3-Bromo-4-hydroxybenzonitrile serves as a key intermediate in the synthesis of various organic compounds, particularly those with potential applications in the chemical, pharmaceutical, and materials science industries. Its unique structure allows for further functionalization and modification, making it a versatile building block for the creation of new molecules with specific properties and functions.
Used in Research and Development:
Due to its unique chemical properties and reactivity, 3-Bromo-4-hydroxybenzonitrile is also utilized in research and development settings. It can be employed in the study of chemical reactions, mechanisms, and the development of new synthetic methods, contributing to the advancement of scientific knowledge and the discovery of novel compounds with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 2315-86-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,1 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2315-86:
(6*2)+(5*3)+(4*1)+(3*5)+(2*8)+(1*6)=68
68 % 10 = 8
So 2315-86-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrNO/c8-6-3-5(4-9)1-2-7(6)10/h1-3,10H
2315-86-8Relevant articles and documents
HCl·DMPU-assisted one-pot and metal-free conversion of aldehydes to nitriles
Hammond, Gerald B.,Mudshinge, Sagar R.,Potnis, Chinmay S.,Xu, Bo
supporting information, p. 4161 - 4164 (2020/07/14)
We report an efficient HCl·DMPU assisted one-pot conversion of aldehydes into nitriles. The use of HCl·DMPU as both an acidic source as well as a non-nucleophilic base constitutes an environmentally mild alternative for the preparation of nitriles. Our protocol proceeds smoothly without the use of toxic reagents and metal catalysts. Diverse functionalized aromatic, aliphatic and allylic aldehydes incorporating various functional groups were successfully converted to nitriles in excellent to quantitative yields. This protocol is characterized by a broad substrate scope, mild reaction conditions, and high scalability. This journal is
Mechanism of bromoxynil phototransformation: Effect of medium and surfactant
Bououden, Zelikha,Halladja, Sabrina,Sleiman, Mohamad,Leremboure, Martin,Richard, Claire
, p. 151 - 156 (2018/08/10)
Bromoxynil (BXN, 3,5-dibromo-4-hydroxybenzonitrile) is a herbicide that is classified as a highly hazardous chemical, toxic for the reproduction. The processes and mechanisms regarding the fate of this compound in the environmental compartments subject to
Intermediates for macrocyclic compounds
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Page/Page column 33; Sheet 8, (2015/11/30)
The present invention is directed to novel macrocyclic compounds of formula (I) and their pharmaceutically acceptable salts, hydrates or solvates: wherein R1, R2, R3, R4, R5, R6, n1, m, p Z1, Z2, and Z3 are as describe in the specification. The invention also relates to compounds of formula (I) which are antagonists of the motilin receptor and are useful in the treatment of disorders associated with this receptor and with or with motility dysfunction.