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N,O-diethyl-N-(3-phenyl-3-[2]pyridyl-propyl)-hydroxylamine is a chemical compound characterized by its hydroxylamine functional group. It is primarily utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals. N,O-diethyl-N-(3-phenyl-3-[2]pyridyl-propyl)-hydroxylamine has demonstrated potential in inhibiting the activity of specific enzymes and has been investigated for its possible anti-cancer and anti-inflammatory properties. Due to its toxicity and potential to cause skin and eye irritation, careful handling and storage are essential. Moreover, precautions should be taken to prevent environmental release, as it may pose risks to aquatic organisms.

104176-77-4

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104176-77-4 Usage

Uses

Used in Pharmaceutical Synthesis:
N,O-diethyl-N-(3-phenyl-3-[2]pyridyl-propyl)-hydroxylamine is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique structure allows it to serve as a building block in the development of novel therapeutic agents.
Used in Agrochemical Synthesis:
In the agrochemical industry, N,O-diethyl-N-(3-phenyl-3-[2]pyridyl-propyl)-hydroxylamine is employed as an intermediate in the production of pesticides and other agricultural chemicals. Its properties make it a valuable component in the creation of effective and targeted products.
Used in Enzyme Inhibition Studies:
N,O-diethyl-N-(3-phenyl-3-[2]pyridyl-propyl)-hydroxylamine is used as a research tool in the study of enzyme inhibition. Its potential to inhibit certain enzymes makes it a valuable asset in the development of new treatments for various diseases and conditions.
Used in Anti-Cancer Research:
N,O-diethyl-N-(3-phenyl-3-[2]pyridyl-propyl)-hydroxylamine has been studied for its potential anti-cancer properties. Researchers are exploring its ability to target and disrupt cancer cell processes, offering a promising avenue for the development of new cancer therapies.
Used in Anti-Inflammatory Research:
N,O-diethyl-N-(3-phenyl-3-[2]pyridyl-propyl)-hydroxylamine is also being investigated for its potential anti-inflammatory properties. Its ability to modulate inflammation could lead to the development of new treatments for inflammatory diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 104176-77-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,1,7 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 104176-77:
(8*1)+(7*0)+(6*4)+(5*1)+(4*7)+(3*6)+(2*7)+(1*7)=104
104 % 10 = 4
So 104176-77-4 is a valid CAS Registry Number.

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