4-Piperidinol, 4-(4-fluorophenyl)-1-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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Basic information
1. Product Name: 4-Piperidinol, 4-(4-fluorophenyl)-1-methyl-
2. Synonyms: 4-(4-fluorophenyl)-4-hydroxy-1-methylpiperidine;
3. CAS NO:36882-06-1
4. Molecular Formula: C12H16FNO
5. Molecular Weight: 209.26000
6. EINECS: N/A
7. Product Categories: N/A
8. Mol File: 36882-06-1.mol
Chemical Properties
1. Melting Point: N/A
2. Boiling Point: 322.7±42.0 °C(Predicted)
3. Flash Point: N/A
4. Appearance: N/A
5. Density: 1.154±0.06 g/cm3(Predicted)
6. Refractive Index: N/A
7. Storage Temp.: N/A
8. Solubility: N/A
9. CAS DataBase Reference: 4-Piperidinol, 4-(4-fluorophenyl)-1-methyl-(CAS DataBase Reference)
10. NIST Chemistry Reference: 4-Piperidinol, 4-(4-fluorophenyl)-1-methyl-(36882-06-1)
11. EPA Substance Registry System: 4-Piperidinol, 4-(4-fluorophenyl)-1-methyl-(36882-06-1)
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: 36882-06-1(Hazardous Substances Data)

36882-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36882-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,8 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36882-06:
(7*3)+(6*6)+(5*8)+(4*8)+(3*2)+(2*0)+(1*6)=141
141 % 10 = 1
So 36882-06-1 is a valid CAS Registry Number.

36882-06-1Upstream product

36882-06-1Downstream Products

36882-06-1Relevant articles and documents

SUBSTITUTED DIHYDROPYRAZOLO PYRAZINE CARBOXAMIDE DERIVATIVES

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Page/Page column 166-167, (2020/01/10)

The invention relates to substituted dihydropyrazolo pyrazine carboxamide derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and diabetes, and also urogenital and ophthalmic disorders.

Improved process for paroxetine hydrochloride substantially free from potential impurities

Gangula, Srinivas,Kolla, Naveen Kumar,Elati, Chandrasekar,Dongamanti, Ashok,Bandichhor, Rakeshwar

experimental part, p. 3344 - 3360 (2012/10/08)

An efficient process for production of paroxetine hydrochloride hemihydrate 1, a selective 5-hydroxytryptamine (serotonin) reuptake inhibitor, is described. Identification and control of potential impurities and establishment of efficient downstream workup procedures enabled us to produce paroxetine hydrochloride hemihydrate 1 efficiently.

Vesicular monoamine transporter substrate/inhibitor activity of MPTP/MPP+ derivatives: A structure-activity study

Wimalasena, D. Shyamali,Perera, Rohan P.,Heyen, Bruce J.,Balasooriya, Inoka S.,Wimalasena, Kandatege

, p. 760 - 768 (2008/09/19)

The active metabolite of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), N-methyl-4-phenylpyridinium (MPP+), selectively destroys the dopaminergic neurons and induces the symptoms of Parkinson's disease. Inhibition of mitochondrial complex

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CAS

36882-06-1