1008-97-5 Usage
Uses
Used in Pharmaceutical Industry:
p-(1-pyrrolidinyl)phenol is used as an intermediate in the production of pharmaceuticals for its potential inhibitory effect on the enzyme monoamine oxidase A. This enzyme plays a crucial role in the metabolism of neurotransmitters like serotonin and dopamine, and its inhibition can have therapeutic benefits in treating various medical conditions.
Used in Agrochemical Industry:
p-(1-pyrrolidinyl)phenol is used as an intermediate in the production of agrochemicals, where it may contribute to the development of new compounds with potential applications in agriculture, such as pest control or crop protection.
Used in Drug Development:
p-(1-pyrrolidinyl)phenol is used as a promising candidate for the development of new drugs due to its anti-inflammatory and analgesic properties. These properties make it a potential candidate for the treatment of various medical conditions, including pain management and inflammation-related disorders.
Further Research:
p-(1-pyrrolidinyl)phenol is used in research settings to explore its potential uses and safety profile. As a compound with multiple pharmacological properties, it requires extensive investigation to fully understand its therapeutic potential and any associated risks before it can be widely adopted in clinical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1008-97-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1008-97:
(6*1)+(5*0)+(4*0)+(3*8)+(2*9)+(1*7)=55
55 % 10 = 5
So 1008-97-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO/c12-10-5-3-9(4-6-10)11-7-1-2-8-11/h3-6,12H,1-2,7-8H2
1008-97-5Relevant academic research and scientific papers
AMINATION AND HYDROXYLATION OF ARYLMETAL COMPOUNDS
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Paragraph 0098; 0226; 0245, (2018/03/25)
In one aspect, the present disclosure provides methods of preparing a primary or secondary amine and hydroxylated aromatic compounds. In some embodiments, the aromatic compound may be unsubstituted, substituted, or contain one or more heteroatoms within the rings of the aromatic compound. The methods described herein may be carried out without the need for transition metal catalysts or harsh reaction conditions.
