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4-METHOXY-4-PHENYLPIPERIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 201609-38-3 Structure
  • Basic information

    1. Product Name: 4-METHOXY-4-PHENYLPIPERIDINE
    2. Synonyms: 4-METHOXY-4-PHENYLPIPERIDINE
    3. CAS NO:201609-38-3
    4. Molecular Formula: C12H17NO
    5. Molecular Weight: 191.26948
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 201609-38-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-METHOXY-4-PHENYLPIPERIDINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-METHOXY-4-PHENYLPIPERIDINE(201609-38-3)
    11. EPA Substance Registry System: 4-METHOXY-4-PHENYLPIPERIDINE(201609-38-3)
  • 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: 201609-38-3(Hazardous Substances Data)

201609-38-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201609-38-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,6,0 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 201609-38:
(8*2)+(7*0)+(6*1)+(5*6)+(4*0)+(3*9)+(2*3)+(1*8)=93
93 % 10 = 3
So 201609-38-3 is a valid CAS Registry Number.

201609-38-3Relevant articles and documents

Propafenone analogue with additional H-bond acceptor group shows increased inhibitory activity on P-glycoprotein

Cseke, Anna,Decker, Simon,Ecker, Gerhard F.,Jain, Sankalp,Schwarz, Theresa,Urban, Ernst,Vogl, Kerstin

, (2020/01/21)

P-glycoprotein (P-gp) is an ATP-dependent efflux pump that has a marked impact on the absorption, distribution, and excretion of therapeutic drugs. As P-gp inhibition can result in drug–drug interactions and altered drug bioavailability, identifying molec

(4-PHENYL-PIPERIDIN-1-YL)-[5-1H-PYRAZOL-4YL)-THIOPHEN-3-YL]-METHANONE COMPOUNDS AND THEIR USE

-

, (2011/04/19)

The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain (4-phenyl-piperidin-1-yl)- [5-(1 H-pyrazol-4-yl)-thiophen-3-yl]-methanone compounds that, inter alia, inhibit 11 β-hydroxysteroid dehydrogenase type 1 (11 β-HSD1 ). The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit 1 1 β-hydroxysteroid dehydrogenase type 1; to treat disorders that are ameliorated by the inhibition of 11 β-hydroxysteroid dehydrogenase type 1; to treat the metabolic syndrome, which includes disorders such as type 2 diabetes and obesity, and associated disorders including insulin resistance, hypertension, lipid disorders and cardiovascular disorders such as ischaemic (coronary) heart disease; to treat CNS disorders such as mild cognitive impairment and early dementia, including Alzheimer's disease; etc.

Cyclic hexapeptides having antibiotic activity

-

, (2008/06/13)

This invention relates to new polypeptide compound represented by general formula (I), wherein R1, R2, R3, R4, R5 and R6 are as defined in the description or a salt thereof which has antimicrobial activities (especially, antifungal activities), inhibitory activity on β-1,3-glucan synthase, to process for preparation thereof, to a pharmaceutical composition comprising the same, and to a method for prophylactic and/or therapeutic treatment of infectious diseases including Pneumocystis carinii infection (e.g. Pneumocystis carinii pneumonia) in a human being or an animal.

Tetrahydrobenzindole compounds

-

, (2010/02/05)

A compound of formula (I) for use in the treatment or prevention of mental diseases A is N, CH, C having a double bond or CR5; each of B and Z is independently N, CH or CR1, with the proviso that A is N when B and/or Z is N; R1, R2, R3, R4and R5and n are as defined in the specification.

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