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CAS

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21315-20-8

2-(2-Methylpropyloxy)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 21315-20-8 Structure

  • Basic information

    1. Product Name: 2-(2-Methylpropyloxy)phenol
    2. Synonyms: 2-(2-Methylpropyloxy)phenol;2-isobutoxyphenol(SALTDATA: FREE);2-isobutoxyphenol
    3. CAS NO:21315-20-8
    4. Molecular Formula: C10H14O2
    5. Molecular Weight: 166.22
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 21315-20-8.mol

  • Chemical Properties

    1. Melting Point: 50-51 °C
    2. Boiling Point: 248.4°C at 760 mmHg
    3. Flash Point: 95.3°C
    4. Appearance: /
    5. Density: 1.027g/cm3
    6. Vapor Pressure: 0.0154mmHg at 25°C
    7. Refractive Index: 1.513
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 9?+-.0.30(Predicted)
    11. CAS DataBase Reference: 2-(2-Methylpropyloxy)phenol(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-(2-Methylpropyloxy)phenol(21315-20-8)
    13. EPA Substance Registry System: 2-(2-Methylpropyloxy)phenol(21315-20-8)

  • 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: 21315-20-8(Hazardous Substances Data)

21315-20-8 Usage

Appearance

Pale yellow oily liquid

Odor

Smoky, phenolic

Common uses

Production of pharmaceuticals, perfume industry

Building block

Synthesis of various organic compounds

Properties

Antimicrobial, antioxidant, anti-inflammatory

Ingredient in

Medical and cosmetic products formulation

Flavoring agent

Used in food industry

Natural occurrence

Found in some plant oils

Industrial and commercial applications

Wide range due to versatile properties

Check Digit Verification of cas no

The CAS Registry Mumber 21315-20-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,1 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21315-20:
(7*2)+(6*1)+(5*3)+(4*1)+(3*5)+(2*2)+(1*0)=58
58 % 10 = 8
So 21315-20-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O2/c1-8(2)7-12-10-6-4-3-5-9(10)11/h3-6,8,11H,7H2,1-2H3

21315-20-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methylpropoxy)phenol

1.2 Other means of identification

Product number -
Other names ghl.PD_Mitscher_leg0.605

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:21315-20-8 SDS

21315-20-8Relevant articles and documents

Tuning the mesomorphic properties of liquid-crystalline dibenzotetraaza[14]annulenes - Discotic nematic phases of tetraalkoxy- substituted derivatives

Grolik, Jaros?aw,Dudek, ?ukasz,Eilmes, Julita

, p. 5127 - 5130 (2012/09/25)

A homologous series of five tetrasubstituted dibenzotetraaza[14]annulene- based discotic mesogens was prepared and studied using polarizing optical microscopy (POM) and differential scanning calorimetry (DSC). A nematic phase was identified for the product bearing two peripheral isobutoxy and two dodecyloxy substituents.

Synthesis of bulky 1,2-dialkoxy- and 1,2,3-trialkoxy-arenes

Stephan, Michel,Zupancic, Borut,Mohar, Barbara

experimental part, p. 6308 - 6315 (2011/09/19)

A large series of bulky 1,2-dialkoxy- and 1,2,3-trialkoxy-benzenes was efficiently prepared via Williamson etherification. Preparation of their contiguous bromine-containing derivatives was also achieved.

INSECTICIDAL CARBAMATES EXHIBITING SPECIES-SELECTIVE INHIBITION OF ACETYLCHOLINESTERASE (AChE)

-

Page/Page column 11, (2009/04/24)

The present invention includes insecticidal carbamates that are useful, for example, for the control of insects, such as mosquitoes, which can be used in applications where exposure to and/or contact with humans is likely. The insecticides of the present invention include phenyl N-methyl carbamates and compositions comprising them that exhibit species-selective inhibition of acetylcholinesterase (AChE) and are preferably toxic to mosquitoes but not humans. Of particular interest are compounds of Formula (I) and Formula (II): Compounds of Formula (I) and Formula (II) are especially suitable for insecticide treated nets and indoor residual spraying for mosquito control.

The Baeyer-Villiger Oxidation of Aromatic Aldehydes and Ketones with Hydrogen Peroxide Catalyzed by Selenium Compounds

Syper, Ludwik

, p. 167 - 172 (2007/10/02)

A series of organoselenium compounds was investigated as activators of hydrogen peroxide in the Baeyer-Villiger oxidation.As a result, a convenient and cheap method for transformation of aromatic aldehydes, having polycondensed ring systems or electron-donating substituents, and polymethoxy derivatives of acetophenone, into phenols was elaborated.This method utilizes hydrogen peroxide activated by areneseleninic acids, as oxidizing agent.

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