67567-41-3 Usage
Chemical Structure
1-(4-Methoxy-2-nitrophenyl)methanamine
Explanation
This structure consists of a phenyl ring (C6H5) with a methoxy group (-OCH3) at the 4th position and a nitro group (-NO2) at the 2nd position. An amine group (-NH2) is attached to the 1st position of the phenyl ring.
Explanation
It is classified as an organic compound because it contains carbon and hydrogen atoms, along with other elements like nitrogen and oxygen.
Explanation
The methoxy group (-OCH3) is an ether, while the nitro group (-NO2) is a functional group that contains a nitrogen atom bonded to two oxygen atoms. These groups are attached to the phenyl ring.
Explanation
Due to its unique structure and properties, 1-(4-Methoxy-2-nitrophenyl)methanamine is used in the synthesis of various pharmaceuticals and other organic compounds. It has potential applications in the fields of medicine, research, and chemical synthesis.
Explanation
The presence of the amine, methoxy, and nitro groups in the molecule allows it to participate in a range of chemical reactions, such as substitution, addition, and elimination reactions.
Explanation
As an organic compound, 1-(4-Methoxy-2-nitrophenyl)methanamine is generally soluble in organic solvents like ethanol, methanol, and acetone.
Explanation
The presence of the nitro group in the molecule can make it sensitive to heat, light, and moisture, which may lead to decomposition or other unwanted reactions.
Explanation
Due to its chemical structure, 1-(4-Methoxy-2-nitrophenyl)methanamine may pose health risks, such as irritation or toxicity, if not handled properly. It may also have environmental risks if released into the environment.
Explanation
To maintain the stability and safety of the compound, it should be stored in a cool, dry, and well-ventilated area, away from heat, light, and moisture.
Classification
Organic compound
Functional Groups
Methoxy and nitro groups
Applications
Pharmaceutical synthesis, organic compounds, medicine, research, and chemical synthesis
Reactivity
Can undergo various chemical reactions
Solubility
Soluble in organic solvents
Stability
May be sensitive to heat, light, and moisture
Hazards
Potential health and environmental risks
Storage
Store in a cool, dry, and well-ventilated area
Check Digit Verification of cas no
The CAS Registry Mumber 67567-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,6 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67567-41:
(7*6)+(6*7)+(5*5)+(4*6)+(3*7)+(2*4)+(1*1)=163
163 % 10 = 3
So 67567-41-3 is a valid CAS Registry Number.
67567-41-3Relevant academic research and scientific papers
Synthesis, stability and optimized photolytic cleavage of 4-methoxy-2-nitrobenzyl backbone-protected peptides
Johnson, Erik C. B.,Kent, Stephen B. H.
, p. 1557 - 1559 (2008/03/12)
We demonstrate the potential of 4-methoxy-2-nitrobenzyl as a Boc chemistry-compatible fully reversible backbone modification for synthetic peptides. The Royal Society of Chemistry 2006.
