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CAS

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163658-33-1

(6-ethylpyridin-2-yl)methanol is a chemical compound with the molecular formula C9H13NO. It is a pyridine derivative featuring an ethyl group attached to the second carbon of the pyridine ring and a hydroxymethyl group attached to the first carbon. (6-ethylpyridin-2-yl)methanol serves as a versatile building block in organic synthesis and pharmaceutical research, enabling the creation of diverse compounds with potential biological activity.

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  • 163658-33-1 Structure

  • Basic information

    1. Product Name: (6-ethylpyridin-2-yl)methanol
    2. Synonyms: (6-ethylpyridin-2-yl)methanol;2-Pyridinemethanol,6-ethyl-(9CI);(2-ethyl-pyridin-6-yl)methanol;2-Pyridinemethanol, 6-ethyl;6-ethyl-2-PyridineMethanol
    3. CAS NO:163658-33-1
    4. Molecular Formula: C8H11NO
    5. Molecular Weight: 137.17904
    6. EINECS: N/A
    7. Product Categories: PYRIDINE
    8. Mol File: 163658-33-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 227.553 °C at 760 mmHg
    3. Flash Point: 91.421 °C
    4. Appearance: /
    5. Density: 1.061 g/cm3
    6. Vapor Pressure: 0.044mmHg at 25°C
    7. Refractive Index: 1.536
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: 13.34±0.10(Predicted)
    11. CAS DataBase Reference: (6-ethylpyridin-2-yl)methanol(CAS DataBase Reference)
    12. NIST Chemistry Reference: (6-ethylpyridin-2-yl)methanol(163658-33-1)
    13. EPA Substance Registry System: (6-ethylpyridin-2-yl)methanol(163658-33-1)

  • 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: 163658-33-1(Hazardous Substances Data)

163658-33-1 Usage

Uses

Used in Organic Synthesis:
(6-ethylpyridin-2-yl)methanol is used as a building block for the synthesis of various organic compounds, leveraging its unique structure to form new chemical entities with potential applications in different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (6-ethylpyridin-2-yl)methanol is utilized as a key intermediate in the development of new drugs, thanks to its ability to be modified to create compounds with potential therapeutic effects.
Used as a Reagent in Chemical Reactions:
(6-ethylpyridin-2-yl)methanol is employed as a reagent, particularly in reactions that involve the formation of carbon-carbon and carbon-heteroatom bonds, facilitating the synthesis of complex molecules.
Used in Agrochemical Development:
(6-ethylpyridin-2-yl)methanol has potential applications in the agrochemical sector, where it may contribute to the development of new pesticides or other agricultural chemicals.
Used as a Flavor and Fragrance Ingredient:
In the flavor and fragrance industry, (6-ethylpyridin-2-yl)methanol may be used to create unique scents or tastes, capitalizing on its chemical properties to enhance or create novel sensory experiences.

Check Digit Verification of cas no

The CAS Registry Mumber 163658-33-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,6,5 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 163658-33:
(8*1)+(7*6)+(6*3)+(5*6)+(4*5)+(3*8)+(2*3)+(1*3)=151
151 % 10 = 1
So 163658-33-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO/c1-2-7-4-3-5-8(6-10)9-7/h3-5,10H,2,6H2,1H3

163658-33-1SDS

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 (6-Ethylpyridin-2-yl)methanol

1.2 Other means of identification

Product number -
Other names (6-ethylpyridin-2-yl)methanol

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:163658-33-1 SDS

163658-33-1Relevant articles and documents

SUBSTITUTED N-(1H-INDAZOL-4-YL)IMIDAZO[1,2-a]PYRIDINE-3-CARBOXAMIDE COMPOUNDS AS TYPE III RECEPTOR TYROSINE KINASE INHIBITORS

-

Page/Page column 89, (2012/06/30)

Compounds of Formula I: and pharmaceutically acceptable salts thereof in which R1, R2, R3, R4, R5 and R6 have the meanings given in the specification, are inhibitors of cFMS and are useful in the treatment of fibrosis, bone-related diseases, cancer, autoimmune disorders, inflammatory diseases, cardiovascular diseases, pain and burns in a mammal

Discovery of ritonavir, a potent inhibitor of HIV protease with high oral bioavailability and clinical efficacy

Kempf, Dale J.,Sham, Hing L.,Marsh, Kennan C.,Flentge, Charles A.,Betebenner, David,Green, Brian E.,McDonald, Edith,Vasavanonda, Sudthida,Saldivar, Ayda,Wideburg, Norman E.,Kati, Warren M.,Ruiz, Lisa,Zhao, Chen,Fino, Lynnmarie,Patterson, Jean,Molla, Akhteruzzaman,Plattner, Jacob J.,Norbeck, Daniel W.

, p. 602 - 617 (2007/10/03)

The structure-activity studies leading to the potent and clinically efficacious HIV protease inhibitor ritonavir are described. Beginning with the moderately potent and orally bioavailable inhibitor A-80987, systematic investigation of peripheral (P3 and P2') heterocyclic groups designed to decrease the rate of hepatic metabolism provided analogues with improved pharmacokinetic properties after oral dosing in rats. Replacement of pyridyl groups with thiazoles provided increased chemical stability toward oxidation while maintaining sufficient aqueous solubility for oral absorption. Optimization of hydrophobic interactions with the HIV protease active site produced ritonavir, with excellent in vitro potency (EC50 = 0.02 μM) and high and sustained plasma concentrations after oral administration in four species. Details of the discovery and preclinical development of ritonavir are described.

RETROVIRAL PROTEASE INHIBITING COMPOUNDS

-

, (2008/06/13)

A retroviral protease inhibiting compound of the formula: STR1 is disclosed wherein R 1, R 2, R 5, R 6, Y m and Y' n are herein defined.

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