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870694-34-1

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870694-34-1 Usage

Description

1-(5-BROMO-2-PYRIDINYL)-1,2-ETHANEDIOL, with the molecular formula C7H7BrNO2, is a chemical compound belonging to the pyridine class and specifically a bromopyridine. This halogenated derivative of pyridine is known for its utility in various chemical reactions and synthesis processes, making it a versatile compound in the fields of pharmaceuticals and agrochemicals. The presence of a hydroxyl group in the molecule endows it with potential enzyme and protein inhibitory properties, which are of significant interest in biochemical and pharmacological research. Furthermore, it has been explored as a building block for the synthesis of other organic compounds.

Uses

Used in Pharmaceutical Applications:
1-(5-BROMO-2-PYRIDINYL)-1,2-ETHANEDIOL is used as an intermediate in the synthesis of pharmaceutical compounds due to its unique chemical structure and reactivity. Its ability to participate in various chemical reactions makes it a valuable component in the development of new drugs.
Used in Agrochemical Applications:
In the agrochemical industry, 1-(5-BROMO-2-PYRIDINYL)-1,2-ETHANEDIOL is used as a starting material for the creation of novel agrochemicals. Its properties allow for the development of compounds with potential applications in pest control and crop protection.
Used in Biochemical Research:
1-(5-BROMO-2-PYRIDINYL)-1,2-ETHANEDIOL is used as a research tool in the field of biochemistry. Its potential as an enzyme and protein inhibitor makes it a valuable asset in studying the mechanisms of various biological processes and the development of targeted therapies.
Used in Organic Synthesis:
As a building block for the synthesis of other organic compounds, 1-(5-BROMO-2-PYRIDINYL)-1,2-ETHANEDIOL is utilized in the development of new chemical entities with diverse applications, ranging from materials science to specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 870694-34-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,6,9 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 870694-34:
(8*8)+(7*7)+(6*0)+(5*6)+(4*9)+(3*4)+(2*3)+(1*4)=201
201 % 10 = 1
So 870694-34-1 is a valid CAS Registry Number.

870694-34-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Ethanediol, 1-(5-bromo-2-pyridinyl)-

1.2 Other means of identification

Product number -
Other names 1,2-ETHANEDIOL, 1-(5-BROMO-2-PYRIDINYL)-

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:870694-34-1 SDS

870694-34-1Downstream Products

870694-34-1Relevant articles and documents

Solubility-driven optimization of (pyridin-3-yl) benzoxazinyl- oxazolidinones leading to a promising antibacterial agent

Guo, Bin,Fan, Houxing,Xin, Qisheng,Chu, Wenjing,Wang, Hui,Huang, Yanqin,Chen, Xiaoyan,Yang, Yushe

, p. 2642 - 2650 (2013/05/09)

The solubility-driven structural modification of (pyridin-3-yl) benzoxazinyl-oxazolidinones is described, which resulted in the development of a new series of benzoxazinyl-oxazolidinone analogues with high antibacterial activity against Gram-positive pathogens, including that against linezolid-resistant strains and low hERG inhibition. With regard to structure-activity relationship (SAR) trends among the various substituents on the pyridyl ring, relatively small and nonbasic substituents were preferable to sterically demanding or basic substituents. Oxazolidinone ring substitution on the pyridyl ring generated analogues with antibacterial activity superior to imidazolidinone ring. Solubility was enhanced by the incorporation of polar groups, especially when compounds were converted to their prodrugs. Among the prodrugs, compound 85 exhibited excellent solubility and a good pharmacokinetic profile. In a MRSA systemic infection model, compound 85 displayed an ED 50 = 5.00 mg/kg, a potency that is 2-fold better than that of linezolid.

3- {4- (PYRIDIN-3-YL) PHENYL} -5- (1H-1, 2, 3-TRIAZOL-1-YLMETHYL) -1, 3-OXAZOLIDIN-2-ONES AS ANTIBACTERIAL AGENTS

-

, (2010/02/15)

Compounds of formula (I), as well as pharmaceutically-acceptable salts and pro-drugs thereof, are disclosed wherein R1, R2, R3, and R4 are defined herein. Also disclosed are processes for making compounds of formula (I) as well as methods of using compounds of formula (I) for treating bacterial infections.

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