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71653-43-5

2-phenylethyl nicotinate is an organic compound that is a derivative of niacin, also known as vitamin B3. It is used in the pharmaceutical and cosmetic industries for its anti-inflammatory, antioxidant, and vasodilatory properties.
Used in Pharmaceutical Industry:
2-phenylethyl nicotinate is used as an anti-inflammatory and antioxidant agent for its skin-soothing effects. It helps to reduce redness, inflammation, and other signs of irritation, making it a popular ingredient in products designed for sensitive or reactive skin.
Used in Cosmetic Industry:
2-phenylethyl nicotinate is used as a vasodilator to improve blood circulation when applied to the skin. It is often included in skincare products for its ability to reduce redness and inflammation. Additionally, its aromatic properties make it a popular choice for adding a pleasant fragrance to cosmetic formulations.

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  • 71653-43-5 Structure

  • Basic information

    1. Product Name: 2-phenylethyl nicotinate
    2. Synonyms: 3-Pyridinecarboxylic acid 2-phenylethyl ester;2-phenylethyl pyridine-3-carboxylate;2-phenylethyl nicotinate
    3. CAS NO:71653-43-5
    4. Molecular Formula: C14H13NO2
    5. Molecular Weight: 227.25852
    6. EINECS: 275-772-7
    7. Product Categories: N/A
    8. Mol File: 71653-43-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 363.6 °C at 760 mmHg
    3. Flash Point: 173.7 °C
    4. Appearance: /
    5. Density: 1.149 g/cm3
    6. Vapor Pressure: 1.78E-05mmHg at 25°C
    7. Refractive Index: 1.573
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 3.14±0.10(Predicted)
    11. CAS DataBase Reference: 2-phenylethyl nicotinate(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-phenylethyl nicotinate(71653-43-5)
    13. EPA Substance Registry System: 2-phenylethyl nicotinate(71653-43-5)

  • 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: 71653-43-5(Hazardous Substances Data)

71653-43-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71653-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,5 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71653-43:
(7*7)+(6*1)+(5*6)+(4*5)+(3*3)+(2*4)+(1*3)=125
125 % 10 = 5
So 71653-43-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO2/c16-14(13-7-4-9-15-11-13)17-10-8-12-5-2-1-3-6-12/h1-7,9,11H,8,10H2

71653-43-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylethyl pyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names Nicotinsaeure-phenaethylester

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:71653-43-5 SDS

71653-43-5Relevant articles and documents

Staudinger’s phosphazene as an efficient esterifying reagent

Dinesh, Murugan,Ranganathan, Raja,Archana, Sivasubramaniyan,Sathishkumar, Murugan,Roshan Banu, Mohamed Sulthan,Ponnuswamy, Alagusundaram

supporting information, p. 1454 - 1460 (2016/09/14)

A new application of Staudinger’s phosphazene as an efficient esterifying reagent is reported. Staudinger’s phosphazene formed in situ by the reaction of organic mono-azide with triphenylphosphine, which is trapped by carboxylic acid, to afford amide exclusively. In contrast, interestingly the same phosphazene behaves in a different way as an efficient esterifying reagent, affording ester under a solvent-free microwave-assisted protocol wherein alcohol is added as the another component in addition to the other reactants. This discovery adds yet another new application of Staudinger’s phosphazene to synthetic chemistry.

Recyclable hypervalent iodine(III) reagent iodosodilactone as an efficient coupling reagent for direct esterification, amidation, and peptide coupling

Tian, Jun,Gao, Wen-Chao,Zhou, Dong-Mei,Zhang, Chi

supporting information; experimental part, p. 3020 - 3023 (2012/08/07)

A hypervalent iodine(III) reagent plays a novel role as an efficient coupling reagent to promote the direct condensation between carboxylic acids and alcohols or amines to provide esters, macrocyclic lactones, amides, as well as peptides without racemization. The regeneration of iodosodilactone (1) can also be readily achieved. The intermediate acyloxyphosphonium ion C from the activation of a carboxylic acid is thought to be involved in the present esterification reaction.

The Use of a Nicotinoyl Group as a Protective Group for Hydroxyl and Amino Functions

Ushida, Satoshi

, p. 59 - 60 (2007/10/02)

The effective use of a nicotinoyl group as an easily introducible and cleavable protective group for hydroxyl and amino groups is described.Deprotection by alkaline hydrolysis is performed after activation by quarternization of pyridine moiety with methyl iodide.

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