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Para Methoxy Phenyl Anisic Acid

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PHYSICAL AND CHEMICAL PROPERTIES

 

 

 

 

 

 


 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 



 










 

 

                                                                                                                  Chemicals  Para Methoxy Phenyl Anisic Acid
Para Methoxy Phenyl Anisic Acid
CAS NO. 89-41-8

CAS NO. 89-41-8

PRODUCT IDENTIFICATION

CAS NO. 89-41-8
4-METHOXY-3-NITROBENZOIC ACID
EINECS NO. 201-906-0
FORMULA C8H7NO5
MOL WT. 197.15
H.S. CODE 2916.39
TOXICITY DERIVATION

SYNONYMS 3-Nitro-p-anisic acid;
3-Nitro-p-anissäure (German); ácido 3-nitro-p-anísico (Spanish); Acide 3-nitro-p-anisique (French); 5-Carboxy-2-methoxynitrobenzene;

CLASSIFICATION

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE
White to pale yellow crystalline powder
MELTING POINT 192 - 194 C
BOILING POINT
SPECIFIC GRAVITY
SOLUBILITY IN WATER Insoluble
AUTOIGNITION
VAPOR DENSITY
VAPOR DENSITY
NFPA RATINGS Health: 1; Flammability: 0; Reactivity: 0
REFRACTIVE INDEX
FLASH POINT

STABILITY Stable under ordinary conditions

APPLICATIONS

Anisole is one of the simplest ether containing aromatic group. But it is different with aromatic compounds like furan where the oxygen is a part of the ring. Anisole, C6H5OCH3 (methyl phenyl ether), is a clear liquid that is soluble in ether and alcohol; insoluble in water; boiling point 155 C. Anisole and its derivatives are used as solvents and in perfumery.

Anisole can be obtained from anise seed. Anisic acid, p-methoxybenzoic acid, is a part of cresol class antiseptic compounds. It is also used as an insect repellent and ovicide. Anisole, anisic acid, and their deivatives are also widely used in chemical reaction as intermediates to obtain target materials such as dyes, pharmaceuticals, perfumes, photoinitiators and agrochemcials.

Nitro- is the prefix indicating presence of the group -NO2. Historically They are abundant in dyes and explosives. Nitro compounds, organic hydrocarbons having one or more NO2 groups bonded via nitrogen to the carbon framework, are versatile intermediate in organic synthesis of;

* Michael addition
* Reduction
* Henry Reaction (Nitro-aldol reaction)
* Nef reaction
* O-Alkylation
* Cycloaddition
* Substitution, Elimination, Conversion reaction
* Alkylation, Acylation, and Halogenation

APPEARANCE

White to slightly yellow crystalline powder
ASSAY (GLC)

99.0% min
LOSS ON DRYING 0.2% max

MELTING POINT
183 C min
TRANSPORTATION
PACKING 50kgs in Fiber Drum

 

Note /Government Notification: These chemicals are designated as those that are used in the manufacture of the controlled substances and are important to the manufacture of the substances. For any (Control Substance) products Import and Export *** subjected to your country government laws /control substance ACT.
Information: The information on this web page is provided to help you to work safely, but it is intended to be an overview of hazards, not a replacement for a full Material Safety Data Sheet (MSDS). MSDS forms can be downloaded from the web sites of many chemical suppliers. ,also that the information on the PTCL Safety web site, where this page was hosted, has been copied onto many other sites, often without permission. If you have any doubts about the veracity of the information that you are viewing, or have any queries, please check the URL that your web browser displays for this page. If the URL begins "www.tajapi.com/www/Denatonium Benzoate.htm/" the page is maintained by the Safety Officer in Physical Chemistry at Oxford University. If not, this page is a copy made by some other person and we have no responsibility for it.
The Controlled Substances Act (CSA) was enacted into law by the Congress of the United States as Title II of the Comprehensive Drug Abuse Prevention and Control Act of 1970.[1] The CSA is the federal U.S. drug policy under which the manufacture, importation, possession, use and distribution of certain substances is regulated. The Act also served as the national implementing legislation for the Single Convention on Narcotic Drugs

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