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5-Chloro-1-methoxy-3-nitrobenzene, also known as 3-Nitro-5-chloroanisole, is an aromatic nitro compound with a molecular formula C7H6ClNO3. It is a pale yellow solid that is soluble in organic solvents and slightly soluble in water, with a melting point of 58-60°C. This chemical compound serves as a versatile building block in the synthesis of various products, including pharmaceuticals, agrochemicals, and dyes.

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  • 55910-07-1 Structure
  • Basic information

    1. Product Name: 5-Chloro-1-methoxy-3-nitrobenzene
    2. Synonyms: 3-Chloro-5-methoxy-1-nitrobenzene;3-Chloro-5-nitroanisole;5-Chloro-1-methoxy-3-nitrobenzene
    3. CAS NO:55910-07-1
    4. Molecular Formula: C7H6ClNO3
    5. Molecular Weight: 187.58044
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 55910-07-1.mol
  • Chemical Properties

    1. Melting Point: 101 °C
    2. Boiling Point: 280.8±20.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.366±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-Chloro-1-methoxy-3-nitrobenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Chloro-1-methoxy-3-nitrobenzene(55910-07-1)
    11. EPA Substance Registry System: 5-Chloro-1-methoxy-3-nitrobenzene(55910-07-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 55910-07-1(Hazardous Substances Data)

55910-07-1 Usage

Uses

Used in Pharmaceutical Industry:
5-Chloro-1-methoxy-3-nitrobenzene is used as an intermediate in the synthesis of drugs for its ability to be chemically modified to create a range of medicinal compounds. Its unique structure allows for the development of new pharmaceuticals with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 5-Chloro-1-methoxy-3-nitrobenzene is used as a precursor in the production of pesticides. Its reactivity and functional groups make it suitable for the creation of compounds that can be used to protect crops from pests and diseases.
Used in Dye Industry:
5-Chloro-1-methoxy-3-nitrobenzene is utilized as a starting material in the manufacture of dyes due to its capacity to be transformed into a variety of colored compounds. This makes it valuable for the production of dyes used in textiles, printing inks, and other applications requiring colorants.
Used in Organic Compounds Synthesis:
Beyond its applications in specific industries, 5-Chloro-1-methoxy-3-nitrobenzene is a key component in the synthesis of other organic compounds. Its versatility in organic chemistry allows it to be a part of numerous chemical reactions, leading to the formation of a wide array of products.
It is important to handle 5-Chloro-1-methoxy-3-nitrobenzene with care due to its potential hazards if not properly managed, emphasizing the need for safety measures in its use and production.

Check Digit Verification of cas no

The CAS Registry Mumber 55910-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,9,1 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55910-07:
(7*5)+(6*5)+(5*9)+(4*1)+(3*0)+(2*0)+(1*7)=121
121 % 10 = 1
So 55910-07-1 is a valid CAS Registry Number.

55910-07-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chlor-3-methoxy-5-nitrobenzol

1.2 Other means of identification

Product number -
Other names 1-chloro-3-methoxy-5-nitro-benzene

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:55910-07-1 SDS

55910-07-1Relevant articles and documents

QUINUCLIDINES FOR MODULATING ALPHA 7 ACTIVITY

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Paragraph 0370; 0372, (2016/02/29)

Provided are substituted quinuclidine compounds, pharmaceutical compositions comprising such compounds, and methods of modulating α7 nicotinic acetylcholine receptors and treating neurological disorders using such compounds.

NEW SUBSTITUTED ARYLSULPHONYLGLYCINES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS

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, (2008/12/07)

The present invention relates to substituted arylsulphonylglycines of general formula (I) wherein R, X, Y and Z are defined as in claim 1, the tautomers, enantiomers, diastereomers, mixtures thereof and salts thereof, which have valuable pharmacological properties, particularly the suppression of the interaction of glycogen phosphorylase a with the GL subunit of glycogen-associated protein phosphatase 1 (PP1 ), and their use as pharmaceutical compositions.

Pyridine, pyrimidine, quinoline, quinazoline, and naphthalene urotensin-II receptor antagonists

-

, (2008/06/13)

The present invention relates to urotensin II receptor antagonists, pharmaceutical compositions containing them and their use.

Synthese von natuerlichen Haloindolen via Hetero-Cope-Umlagerung von Vinyl-N-phenylhydroxamaten

Martin, Pierre

, p. 344 - 347 (2007/10/02)

An efficient method for the synthesis of natural 4-chloro-6-methoxyindole (the promutagen from fava beans) and of the two 4,6-dibromo- and 3,4,6-tribromoindoles (produced by acorn worms, Enteropneusta) is presented.The key step is a hetero-Cope rearrangem

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