(1E)-3-Methoxy-3-oxo-1-phenylprop-1-en-1-yl benzoate

Base Information

Chemical Name:(1E)-3-Methoxy-3-oxo-1-phenylprop-1-en-1-yl benzoate
CAS No.:6334-16-3
Molecular Formula:C₁₇H₁₄O₄
Molecular Weight:282.296
Hs Code.:
NSC Number:15166
DSSTox Substance ID:DTXSID10421343
Wikidata:Q82232805

Synonyms:6334-16-3;DTXSID10421343;NSC15166;NSC-15166;(1E)-3-Methoxy-3-oxo-1-phenylprop-1-en-1-yl benzoate

Suppliers and Price of (1E)-3-Methoxy-3-oxo-1-phenylprop-1-en-1-yl benzoate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of (1E)-3-Methoxy-3-oxo-1-phenylprop-1-en-1-yl benzoate

Chemical Property:

Vapor Pressure:2.32E-07mmHg at 25°C
Boiling Point:423°Cat760mmHg
Flash Point:212.9°C
Density:1.195g/cm³
XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:282.08920892
Heavy Atom Count:21
Complexity:388

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC(=O)C=C(C1=CC=CC=C1)OC(=O)C2=CC=CC=C2
Isomeric SMILES:COC(=O)/C=C(\C1=CC=CC=C1)/OC(=O)C2=CC=CC=C2

Technology Process of (1E)-3-Methoxy-3-oxo-1-phenylprop-1-en-1-yl benzoate

There total 4 articles about (1E)-3-Methoxy-3-oxo-1-phenylprop-1-en-1-yl benzoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 115144-90-6
3,3-dimethoxy-1-phenyl-propenone

: 6334-16-3
β-benzoyloxy-cinnamic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous HCl

2: pyridine

With pyridine; hydrogenchloride;
DOI:10.1021/ja01604a037

Reference yield:

: 98-88-4
benzoyl chloride

: 6334-16-3
β-benzoyloxy-cinnamic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

2: aqueous HCl

3: pyridine

With pyridine; hydrogenchloride;
DOI:10.1021/ja01604a037