63010-11-7 Usage
Structure
Substituted cyclopentylamine derivative with a methylphenyl group attached to the cyclopentyl ring
Synonyms
4-Methylcyclopentyl(methylphenyl)methylamine
Applications
a. Organic synthesis
b. Medicinal chemistry
c. Pharmaceutical intermediate
d. Development of new drugs
Potential uses
Varies depending on the specific context in which it is employed
Chemical properties
a. Basicity due to the presence of the amine group
b. Reactivity with electrophiles due to the presence of the cyclopentyl and methylphenyl groups
c. Solubility in organic solvents
Appearance
Likely a liquid or solid, depending on the temperature
Boiling point
Not provided, but can be estimated based on molecular size and structure
Melting point
Not provided, but can be estimated based on molecular size and structure
Density
Not provided, but can be estimated based on molecular size and structure
Polarity
Likely polar due to the presence of the amine group and the aromatic ring
Safety and handling
a. May be sensitive to moisture or air
b. Should be stored in a sealed container, away from light and heat
c. Proper personal protective equipment (PPE) should be used when handling 1-[1-(4-methylphenyl)cyclopentyl]methylamine
d. Specific safety information should be obtained from the material safety data sheet (MSDS) or supplier
Environmental impact
Not provided, but should be considered when handling and disposing of 1-[1-(4-methylphenyl)cyclopentyl]methylamine
Regulatory status
Not provided, but may be subject to specific regulations depending on its intended use and location
Check Digit Verification of cas no
The CAS Registry Mumber 63010-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,1 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63010-11:
(7*6)+(6*3)+(5*0)+(4*1)+(3*0)+(2*1)+(1*1)=67
67 % 10 = 7
So 63010-11-7 is a valid CAS Registry Number.
63010-11-7Relevant articles and documents
Synthesis and biologic activity of aryloxyaminopropanoles based on substituted p-tolylalkylamines
Aghekyan,Mkryan,Tsatinyan,Noravyan,Gasparyan
, p. 209 - 213 (2016/04/19)
Reaction of 2,2-dimethyl-2-(p-tolyl)ethyl-, 1-p-tolylcyclopenthylmethyl- and 4-(p-tolyl)tetrahydro-2H-pyran-4-ylmethylamines with phenoxymethyloxiranes substituted in the aromatic ring afforded new aryloxypropanolamines, some of which show moderate adrenoblocking activity.
