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2-(2-Methoxyphenoxy)-1-(4-methoxyphenyl)ethanone - ≥95%, high purity , CAS No.19513-80-5

    Grade & Purity:
  • ≥95%
In stock
Item Number
M302672
Grouped product items
SKU Size
Availability
Price Qty
M302672-100mg
100mg
3
$41.90
M302672-250mg
250mg
3
$68.90
M302672-1g
1g
3
$184.90
M302672-5g
5g
4
$453.90

Basic Description

Synonyms 2-(2-methoxyphenoxy)-1-(4-methoxyphenyl)ethanone | 19513-80-5 | MFCD00156673 | 2-(2-Methoxyphenoxy)-4'-methoxyacetophenone | Enamine_001107 | Oprea1_496424 | SCHEMBL5947939 | HMS1397C07 | AKOS001012391 | CS-W001019 | DS-9470 | SY046092 | F14632 | A925136 | SR-01000401456 | 4'-METHOXY-
Specifications & Purity ≥95%
Storage Temp Room temperature
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic oxygen compounds
Class Organooxygen compounds
Subclass Carbonyl compounds
Intermediate Tree Nodes Ketones - Aryl ketones - Phenylketones
Direct Parent Alkyl-phenylketones
Alternative Parents Phenoxy compounds  Methoxybenzenes  Benzoyl derivatives  Aryl alkyl ketones  Anisoles  Alkyl aryl ethers  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Alkyl-phenylketone - Phenoxy compound - Methoxybenzene - Aryl alkyl ketone - Phenol ether - Benzoyl - Anisole - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Ether - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.
External Descriptors Not available

Names and Identifiers

Pubchem Sid 504760110
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504760110
IUPAC Name 2-(2-methoxyphenoxy)-1-(4-methoxyphenyl)ethanone
INCHI InChI=1S/C16H16O4/c1-18-13-9-7-12(8-10-13)14(17)11-20-16-6-4-3-5-15(16)19-2/h3-10H,11H2,1-2H3
InChIKey XZENRLBGEKSCQB-UHFFFAOYSA-N
Smiles COC1=CC=C(C=C1)C(=O)COC2=CC=CC=C2OC
Isomeric SMILES COC1=CC=C(C=C1)C(=O)COC2=CC=CC=C2OC
Molecular Weight 272.3
Reaxy-Rn 2292520
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2292520&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot Number Certificate Type Date Item
I2202031 Certificate of Analysis Jun 10, 2025 M302672
I2202032 Certificate of Analysis Jun 10, 2025 M302672
I2202029 Certificate of Analysis Jun 10, 2025 M302672
I2202030 Certificate of Analysis Jun 10, 2025 M302672

Chemical and Physical Properties

Boil Point(°C) 436.5°C at 760 mmHg
Molecular Weight 272.290 g/mol
XLogP3 3.200
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 6
Exact Mass 272.105 Da
Monoisotopic Mass 272.105 Da
Topological Polar Surface Area 44.800 Ų
Heavy Atom Count 20
Formal Charge 0
Complexity 297.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Ruijin Li, Danlian Huang, Lei Lei, Sha Chen, Yashi Chen, Guangfu Wang, Li Du, Wei Zhou, Jiaxi Tao, Haojie Chen.  (2023)  Lignin and metal–organic frameworks: mutual partners on the road to sustainability.  Journal of Materials Chemistry A,  11  (6): (2595-2617). 
2. Kuiyuan Cao, Fang Yang, He Wan, Xixin Duan, Junyou Shi, Zhong Sun.  (2025)  A selective oxidative depolymerization of larch lignin to ethyl vanillate by multifunctional catalysts combining alkaline ionic liquid and polyoxometalates with hydrogen peroxide.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  295  (139642). 

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