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Pyridine, 2-butoxy-5-nitro(7CI,9CI), also known as 2-Butoxy-5-nitro-pyridine, is a chemical compound with the molecular formula C9H12N2O3. It is a nitro-substituted pyridine derivative featuring a butoxy group attached to the second position of the pyridine ring. Known for its strong aromatic odor, Pyridine, 2-butoxy-5-nitro- (7CI,9CI) is classified as a hazardous chemical, necessitating careful handling and storage.

6627-95-8

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6627-95-8 Usage

Uses

Used in Pharmaceutical Industry:
Pyridine, 2-butoxy-5-nitro(7CI,9CI) is utilized as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, Pyridine, 2-butoxy-5-nitro(7CI,9CI) serves as an intermediate in the production of agrochemicals. Its properties make it suitable for the synthesis of compounds used in pest control and crop protection, thereby supporting agricultural productivity.
Used in Organic Compounds Synthesis:
Pyridine, 2-butoxy-5-nitro(7CI,9CI) is employed as a building block for the production of other organic compounds. Its versatile structure enables its use in the creation of a wide range of specialty chemicals, expanding the possibilities in organic synthesis.
Used in Research Applications:
Pyridine, 2-butoxy-5-nitro(7CI,9CI) also finds use in research settings, where it can be employed as a research compound. Its unique properties make it valuable for studying various chemical reactions and exploring new areas of chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 6627-95-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6627-95:
(6*6)+(5*6)+(4*2)+(3*7)+(2*9)+(1*5)=118
118 % 10 = 8
So 6627-95-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O3/c1-2-3-6-14-9-5-4-8(7-10-9)11(12)13/h4-5,7H,2-3,6H2,1H3

6627-95-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butoxy-5-nitropyridine

1.2 Other means of identification

Product number -
Other names 2-Butoxy-5-Nitro-Pyridine

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:6627-95-8 SDS

6627-95-8Relevant academic research and scientific papers

PIPERAZINE AND PIPERIDINE MGLUR5 POTENTIATORS

-

Page/Page column 42, (2008/12/07)

Compounds of Formula I or pharmaceutically acceptable salts or solvates thereof, wherein A, B, D, Ar1, Ar2, R2, R3, R4, a, m and n are defined in the specification, methods for the use thereof, processes for making and pharmaceutical compositions containing the same.

Liquid Crystalline Compounds Bearing Pyridine Ring: 3-(4-Alkoxyphenylazoxy)-6-alkoxypyridines

Kamogawa, Hiroyoshi,Kasai, Tsuneharu

, p. 69 - 78 (2007/10/02)

3-(4-Alkoxyphenylazo)-6-alkoxypyridines (6) with n-alkoxyl (C1-C6) groups were synthesized by the coupling reaction of phenol with 6-alkoxy-3-pyridine diazonium chloride prepared from 2-chloro-5-nitropyridine via 2-alkoxy-5-nitro and 2-alkoxy-5-aminopyridines and subsequent etherification with n-alkyl iodides.Mild oxidation of 6 with hydrogen peroxide in acetic acid provided 3-6-alkoxy-pyridines (7) containing nearly equimolar amounts of ONN (8) and NNO (8') isomers.Centrifugal liquid chromatography satisfactorily separated these two isomers.Mesomorphic behaviors of 8 and 8' are characteristic in that the pyridine ring exerts polar effects and 8 are more balanced in polarity than 8'.Compounds 7 possess rather lower mesomorphic ranges than 8 and 8'.Some of compounds 6 indicate mesomorphic ranges but generally azo compounds are inferior to azoxy ones.

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