79944-62-0

Usage

Uses

Used in Synthetic Chemistry:
(3-Chloro-5-nitrophenyl)methanol is used as a key intermediate in the synthesis of several chemical products. Its unique structure allows it to be a valuable building block for creating a wide range of compounds in the field of synthetic chemistry.
Used in Pharmaceutical Industry:
(3-Chloro-5-nitrophenyl)methanol is used as a starting material for the development of new pharmaceutical compounds. Its reactivity and structural features make it a promising candidate for the synthesis of potential drug molecules, contributing to the advancement of medicinal chemistry.
Used in Chemical Research:
(3-Chloro-5-nitrophenyl)methanol is used as a research tool in various chemical studies. Its properties and reactivity are of interest to scientists who aim to understand the behavior of similar compounds and explore their potential applications in different fields.
Used in Material Science:
(3-Chloro-5-nitrophenyl)methanol is used as a component in the development of new materials with specific properties. Its incorporation into the synthesis process can lead to the creation of materials with unique characteristics, such as improved stability or enhanced reactivity, which can be beneficial in various applications.

InChI:InChI=1/C7H6ClNO3/c8-6-1-5(4-10)2-7(3-6)9(11)12/h1-3,10H,4H2

Upstream product

• 90390-46-8 (3-amino-5-nitrophenyl)methanol 
• 34662-36-7 3-chloro-5-nitrobenzoic acid 
• 71022-43-0 3,5-dinitrobenzyl alcohol 
• 36138-28-0 3-chloro-5-nitro-benzoic acid methyl ester 

Downstream Products

• 284047-89-8 3-chloro-5-N,N-dimethylaminobenzyl alcohol 
• 284047-83-2 3-chloro-5-nitromandelic acid 
• 960083-35-6 4-(3-chloro-5-nitro-phenyl)-1H-pyrrole-3-carbonitrile 
• 960083-34-5 3-(3-chloro-5-nitro-phenyl)-acrylonitrile 
• 90390-41-3 Butyl-(3-chloro-5-nitro-benzyl)-amine 
• 90390-40-2 (3-Chloro-5-nitro-benzyl)-propyl-amine 
• 90390-39-9 (3-Chloro-5-nitro-benzyl)-ethyl-amine 
• 90390-38-8 (3-Chloro-5-nitro-benzyl)-methyl-amine 
• 90390-37-7 Butyl-(3-chloro-5-fluoro-benzyl)-amine 
• 90390-36-6 (3-Chloro-5-fluoro-benzyl)-propyl-amine 
• 90390-35-5 (3-Chloro-5-fluoro-benzyl)-ethyl-amine 
• 90390-34-4 (3-Chloro-5-fluoro-benzyl)-methyl-amine 
• 90390-48-0 3-chloro-5-(hydroxymethyl)benzenediazonium tetrafluoroborate 
• 79944-64-2 (3-chloro-5-fluorophenyl)methanol 

Relevant academic research and scientific papers

4-(ORTHO)-FLUOROPHENYL-5-FLUOROPYRIMIDIN-2-YL AMINES CONTAINING A SULFOXIMINE GROUP

The present invention relates to 4-(ortho)-fluorophenyl-5-fluoropyrimidin-2-yl amine derivatives containing a sulfoximine group of general formula (I) as described and defined herein, and methods for their preparation, their use for the treatment and/or p

DISUBSTITUTED 5-FLUORO PYRIMIDINE DERIVATIVES CONTAINING A SULFOXIMINE GROUP

The present invention relates to disubstituted 5-fluoro pyrimidine derivatives containing a sulfoximine group of general formula (I) as described and defined herein, and methods for their preparation, their use for the treatment and/or prophylaxis of diso

PYRROLE DERIVATIVES WITH CRTH2 RECEPTOR MODULATOR ACTIVITY

There are provided according to the invention compounds of formula (I) in free or salt form, wherein R3, R 4, R5, R6a, R6b, Q and W are as described in the specification, process for preparing them, a

Synthesis and structure-activity relationships of 3-aminobenzophenones as antimitotic agents

A new series of 3-aminobenzophenone compounds as potent inhibitors of tubulin polymerization was discovered based on the mimic of the aminocombretastatin molecular skeleton. Lead compounds 5 and 11, with alkoxy groups at the C-4 position of B-ring, were p

Enzymatic resolution of substituted mandelic acids

A series of substituted mandelic acids were prepared and subjected to enzymatic resolution utilizing Lipase PS 'Amano'.

New amidino derivatives and their use as thormbin inhibitors

There is provided compounds of formula I, wherein Y and R1 have meanings given in the description, and pharmaceutically acceptable derivatives (including prodrugs) thereof, which compounds and derivatives are useful as, or are useful as prodrugs of, competitive inhibitors of trypsin-like proteases, such as thrombin, and thus, in particular, in the treatment of conditions where inhibition of thrombin is required (e.g. thrombosis) or as anticoagulants.

Benzylamines: Synthesis and evaluation of antimycobacterial properties

The synthesis of benzylamines with various N-alkyl chains and substituents in the aromatic system as well as their evaluation on Mycobacterium tuberculosis H 37 Ra are described. The most active compounds in this test, N-methyl-3-chlorobenzylamine (MIC 10.2 μg/mL), N-methyl-3,5-dichlorobenzylamine (93, MIC 10.2 μg/mL), and N-butyl-3,5-difluorobenzylamine (MIC 6.4 μg/mL), also exhibited a marked inhibitory effect on Mycobacterium marinum and Mycobacterium lufu used for the determination of antileprotic properties. The combination of 93 with aminosalicylic acid, streptomycin, or dapsone exert marked supra-additive effects on M. tuberculosis H 37 Ra.