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3-Piperidinemethanol, 4-(4-fluorophenyl)-1-methyl-, (3R,4R)-, commonly known as Lorcaserin, is a chemical compound that was initially developed as a weight loss medication. It functions as a selective serotonin 2C receptor agonist, which was approved by the FDA in 2012 for the treatment of obesity. Lorcaserin operates by stimulating the serotonin receptors in the brain, thereby suppressing appetite and inducing a sense of satiety, which results in decreased food consumption and weight reduction. However, due to emerging safety concerns, particularly regarding an increased risk of cancer, Lorcaserin was removed from the market in 2020.

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  • 100332-12-5 Structure
  • Basic information

    1. Product Name: 3-Piperidinemethanol, 4-(4-fluorophenyl)-1-methyl-, (3R,4R)-
    2. Synonyms:
    3. CAS NO:100332-12-5
    4. Molecular Formula: C13H18FNO
    5. Molecular Weight: 223.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100332-12-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-Piperidinemethanol, 4-(4-fluorophenyl)-1-methyl-, (3R,4R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Piperidinemethanol, 4-(4-fluorophenyl)-1-methyl-, (3R,4R)-(100332-12-5)
    11. EPA Substance Registry System: 3-Piperidinemethanol, 4-(4-fluorophenyl)-1-methyl-, (3R,4R)-(100332-12-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 100332-12-5(Hazardous Substances Data)

100332-12-5 Usage

Uses

Used in Pharmaceutical Industry:
3-Piperidinemethanol, 4-(4-fluorophenyl)-1-methyl-, (3R,4R)was used as a weight loss medication for the treatment of obesity. It was utilized as a selective serotonin 2C receptor agonist for its appetite-suppressing and satiety-inducing effects, which contributed to reduced food intake and weight loss.
However, due to the withdrawal of Lorcaserin from the market in 2020, its applications in the pharmaceutical industry have been discontinued. The safety concerns that led to its withdrawal highlight the importance of ongoing monitoring and evaluation of pharmaceutical products to ensure patient safety and efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 100332-12-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,3 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100332-12:
(8*1)+(7*0)+(6*0)+(5*3)+(4*3)+(3*2)+(2*1)+(1*2)=45
45 % 10 = 5
So 100332-12-5 is a valid CAS Registry Number.

100332-12-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R,4R)-4-(4-Fluorophenyl)-3-hydroxymethyl-1-methylpiperidine

1.2 Other means of identification

Product number -
Other names (+)-cis-4-(4-fluorophenyl)-3-hydroxymethyl-1-methylpiperidine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:100332-12-5 SDS

100332-12-5Upstream product

100332-12-5Downstream Products

100332-12-5Relevant articles and documents

Process for the preparation of optically enriched 4-aryl-3-hydromethyl substituted piperidines to be used as intermediates in the synthesis of paroxetine

-

, (2008/06/13)

The subject invention pertains to optically-enriched compounds of formula (1), wherein Ar is a C6-20 aryl group; and R1 and R2 are independently H, alkyl or aryl. The subject invention also pertains to method of preparing these compounds. The subject compounds can be prepared by reduction of the corresponding 1,4-dihydropyridine-3-aldehyde, e.g., using hydrogen an a catalyst. The aldehyde can be prepared by hydrolytic cleavage of an aminal obtainable by the reaction of 3-pyridinecarboxaldehyde and a chiral C-2 symmetric diamine, an then stereoselective introduction of the Ar and COOCHR1 R2 groups. STR1

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