BETA-OXO-3-(PHENYLMETHOXY)-BENZENEPROPANOIC ACID METHYL ESTER

Base Information

Chemical Name:BETA-OXO-3-(PHENYLMETHOXY)-BENZENEPROPANOIC ACID METHYL ESTER
CAS No.:150356-53-9
Molecular Formula:C₁₇H₁₆O₄
Molecular Weight:284.312
Hs Code.:
Mol file:150356-53-9.mol

Synonyms:methyl 3-(3-(benzyloxy)phenyl)-3-oxopropanoate

Suppliers and Price of BETA-OXO-3-(PHENYLMETHOXY)-BENZENEPROPANOIC ACID METHYL ESTER

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

TRC
Methyl3-(3-(Benzyloxy)phenyl)-3-oxopropanoate
10mg
$ 85.00

TRC
Methyl3-(3-(Benzyloxy)phenyl)-3-oxopropanoate
5mg
$ 55.00

AK Scientific
Methyl3-[3-(Benzyloxy)phenyl]-3-oxopropionate
1g
$ 937.00

Total 2 raw suppliers

Chemical Property of BETA-OXO-3-(PHENYLMETHOXY)-BENZENEPROPANOIC ACID METHYL ESTER

Chemical Property:

Boiling Point:404.2±25.0 °C(Predicted)
PKA:10.25±0.46(Predicted)
Density:1.174±0.06 g/cm3(Predicted)

Purity/Quality:

97% ^*data from raw suppliers

Methyl3-(3-(Benzyloxy)phenyl)-3-oxopropanoate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses Methyl 3-(3-(Benzyloxy)phenyl)-3-oxopropanoate is an intermediate in the synthesis of β-(m-Hydroxyphenyl)hydracrylic Acid (H949280). β-(m-Hydroxyphenyl)hydracrylic Acid is a urinary metabolite of phenylalanine from the Clostridium gram-positive bacteria cell line. Urinary metabolite of Rutin (R701800), a capillary protectant in plants.

Technology Process of BETA-OXO-3-(PHENYLMETHOXY)-BENZENEPROPANOIC ACID METHYL ESTER

There total 4 articles about BETA-OXO-3-(PHENYLMETHOXY)-BENZENEPROPANOIC ACID METHYL ESTER 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: 97.0%

: 34068-01-4
1-[3-(phenylmethoxy)phenyl]ethan-1-one

: 150356-53-9
methyl 3-(3-(benzyloxy)phenyl)-3-oxopropanoate

Guidance literature:: In hydrogenchloride; carbonic acid dimethyl ester; mineral oil;

Reference yield: 80.0%

: 34068-01-4
1-[3-(phenylmethoxy)phenyl]ethan-1-one

: 616-38-6
carbonic acid dimethyl ester

: 150356-53-9
methyl 3-(3-(benzyloxy)phenyl)-3-oxopropanoate

Guidance literature:: 1-[3-(phenylmethoxy)phenyl]ethan-1-one; With sodium hydride; In tetrahydrofuran; mineral oil; at 0 ℃; for 0.166667h; Inert atmosphere;

carbonic acid dimethyl ester; In tetrahydrofuran; mineral oil; at 60 - 70 ℃; for 12h; Inert atmosphere;

Reference yield:

: 121-71-1
3-Hydroxyacetophenone

: 150356-53-9
methyl 3-(3-(benzyloxy)phenyl)-3-oxopropanoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium iodide; potassium carbonate / acetone / 20 h / 70 °C

2.1: sodium hydride / tetrahydrofuran; mineral oil / 0.17 h / 0 °C / Inert atmosphere

2.2: 12 h / 60 - 70 °C / Inert atmosphere

With sodium hydride; potassium carbonate; potassium iodide; In tetrahydrofuran; acetone; mineral oil;