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1-(4-fluorophenyl)-4-(morpholin-4-yl)butan-1-one hydrochloride is a chemical compound with the molecular formula C16H20ClFNO2. It is a derivative of 1-(4-fluorophenyl)-4-(morpholin-4-yl)butan-1-one, which is a ketone containing a 4-fluorophenyl group and a morpholin-4-yl group. The hydrochloride salt form is obtained by treating the parent compound with hydrochloric acid, resulting in the addition of a chloride ion and a proton to the molecule. 1-(4-fluorophenyl)-4-(morpholin-4-yl)butan-1-one hydrochloride is often used in pharmaceutical applications, particularly as an intermediate in the synthesis of various drugs. It is known for its potential role in the development of medications targeting central nervous system disorders, due to its ability to modulate certain receptors or enzymes. The hydrochloride salt form enhances the solubility and stability of the compound, which can be crucial for its pharmaceutical utility.

1219-37-0

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1219-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1219-37-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1219-37:
(6*1)+(5*2)+(4*1)+(3*9)+(2*3)+(1*7)=60
60 % 10 = 0
So 1219-37-0 is a valid CAS Registry Number.

1219-37-0Relevant academic research and scientific papers

HETEROAROMATIC COMPOUNDS, METHOD FOR PREPARING THE COMPOUNDS, PHARMACEUTICAL COMPOSITIONS, USES AND METHOD FOR TREATING ACUTE AND CHRONIC PAIN

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Paragraph 0160, (2015/09/22)

The present invention refers to a compound of formula (I) or a pharmaceutically acceptable salt thereof, having analgecic activity. Particularly, the compounds of the instant invention are useful to treat or prevent acute and chronic pain, especially neuropathic pain. Additionally, the present invention provides a procces for preparing the compounds, a pharmaceutical composition that comprises a compound of formula (I), and a method for treatment of acute and chronic pain.

N-substituted alpha-aminoalkylacrylophenones and some related compounds: a new class of spermicidal agents.

Gupta,Nautiyal,Jhingran,Kamboj,Setty,Anand

, p. 303 - 307 (2007/10/02)

The results of a screening program to test the spermicidal effectiveness of several compounds is presented. The program was initiated after N-substituted 3-aminoacrylophenones were found to have unexpected spermicidal activity. The compounds had been synthesized as possible antiinflammatory agents. This result prompted the synthesis and screening of N-substituted alpha-aminomethylacrylophenones, alpha-(2-aminomethyl)acrylophenones and 3-N-substituted-2-methyleneindan-1-ones. The starting materials, substituted acetophenones, for the synthesis of N-substituted alpha-aminomethylacrylophenones were either commercial products or obtained by standard methods. N-substituted amino-butyrophenone was reacted with paraformaldehyde to yield the alpha-(2 aminoethyl)acrylophenones. A series of reactions was undertaken to synthesize 2-methyleneindan-1-ones. The preparation of each is detailed and molecular formulas are provided. Spermicidal activity was assessed by dissolving the compound in physiological saline at different concentrations. 2 drops of rat sperm suspension or human semen were placed on a slide, followed by 2 drops of a compound solution. Control slides of physiological saline were prepared. The contents were mixed for approximately 5 seconds and examined under a phase contrast microscope. The results were considered positive if 100% of the spermatozoa became immotile instantaneously. Several of the compounds showed marked spermicidal activity.

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