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802559-15-5

2-Phenyl-3-piperidin-1-yl-propan-1-ol is a chemical compound belonging to the class of organic compounds known as benzenoids. It is characterized by a molecular formula of C14H21NO and a molecular weight of 221.322 g/mol. 2-PHENYL-3-PIPERIDIN-1-YL-PROPAN-1-OL's structure includes a phenyl group, which is a ring of six carbon atoms, as well as a piperidine ring and a propanol group. However, there is currently limited information available on its properties, uses, or effects. As a result, it is essential to exercise appropriate handling and safety measures when working with this compound, and further research may be necessary to fully understand its characteristics and potential applications.

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  • 802559-15-5 Structure

  • Basic information

    1. Product Name: 2-PHENYL-3-PIPERIDIN-1-YL-PROPAN-1-OL
    2. Synonyms: 1-Piperidinepropanol, .beta.-phenyl-
    3. CAS NO:802559-15-5
    4. Molecular Formula: C14H21NO
    5. Molecular Weight: 219.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 802559-15-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 347.8°C at 760 mmHg
    3. Flash Point: 163°C
    4. Appearance: /
    5. Density: 1.041g/cm3
    6. Vapor Pressure: 1.98E-05mmHg at 25°C
    7. Refractive Index: 1.545
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 14.72±0.10(Predicted)
    11. CAS DataBase Reference: 2-PHENYL-3-PIPERIDIN-1-YL-PROPAN-1-OL(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-PHENYL-3-PIPERIDIN-1-YL-PROPAN-1-OL(802559-15-5)
    13. EPA Substance Registry System: 2-PHENYL-3-PIPERIDIN-1-YL-PROPAN-1-OL(802559-15-5)

  • 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: 802559-15-5(Hazardous Substances Data)

802559-15-5 Usage

Uses

Due to the limited information available on 2-Phenyl-3-piperidin-1-yl-propan-1-ol, its specific applications are not well-defined. However, given its classification as a benzenoid compound, it may have potential uses in various industries, such as pharmaceuticals, materials science, or chemical research. Further studies and investigations are required to determine its exact applications and benefits. Until more information is available, it is recommended to handle this compound with caution and adhere to proper safety protocols.

Check Digit Verification of cas no

The CAS Registry Mumber 802559-15-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,2,5,5 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 802559-15:
(8*8)+(7*0)+(6*2)+(5*5)+(4*5)+(3*9)+(2*1)+(1*5)=155
155 % 10 = 5
So 802559-15-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H21NO/c16-12-14(13-7-3-1-4-8-13)11-15-9-5-2-6-10-15/h1,3-4,7-8,14,16H,2,5-6,9-12H2

802559-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-3-piperidin-1-ylpropan-1-ol

1.2 Other means of identification

Product number -
Other names 1-Piperidinepropanol,b-phenyl

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:802559-15-5 SDS

802559-15-5Upstream product

802559-15-5Downstream Products

802559-15-5Relevant articles and documents

Catalytic Asymmetric Synthesis of N-Chiral Amine Oxides

Bhadra, Sukalyan,Yamamoto, Hisashi

supporting information, p. 13043 - 13046 (2016/10/30)

Direct asymmetric synthesis of N-chiral amine oxides was accomplished (up to 91:9 e.r.) by means of a bimetallic titanium catalyst. A hydroxy group situated at the γ-position of the N stereocenter enables the desired N-oxidation through dynamic kinetic resolution of the trivalent amine substrates. The method was further extended to the kinetic resolution of racemic γ-amino alcohols with a preexisting stereocenter, giving an important class of enantioenriched (up to 99.9:0.1 e.r.) building blocks that are otherwise difficult to synthesize.

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