4-O-Feruloylquinic acid

Base Information

Chemical Name:4-O-Feruloylquinic acid
CAS No.:2613-86-7
Molecular Formula:C₁₇H₂₀O₉
Molecular Weight:368.34
Hs Code.:

Synonyms:4-O-feroluoylquinic acid

Suppliers and Price of 4-O-Feruloylquinic acid

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

Arctom
4-O-Feruloylquinicacid ≥98%
5mg
$ 448.00

Total 22 raw suppliers

Chemical Property of 4-O-Feruloylquinic acid

Chemical Property:

Melting Point:195-196 °C(Solv: water (7732-18-5))
Boiling Point:656.1±55.0 °C(Predicted)
PKA:4.07±0.50(Predicted)
Density:1.53±0.1 g/cm3(Predicted)

Purity/Quality:

≥98% ^*data from raw suppliers

4-O-Feruloylquinicacid ≥98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 4-O-Feruloylquinic Acid is a methanolic extract of Murraya Paniculata leaves that exhibits antioxidant and antimicrobial properties against fungi, gram positive and gram negative bacteria.

Technology Process of 4-O-Feruloylquinic acid

There total 5 articles about 4-O-Feruloylquinic acid 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:

: (1R,3R,4S,5R)-4-[3-(4-acetoxy-3-methoxyphenyl)acryloyloxy]-5-tert-butyldimethylsiloxy-1-hydroxycyclohexane-1,3-carbolactone

: 2613-86-7
4-O-feroluoylquinic acid

Guidance literature:: (1R,3R,4S,5R)-4-[3-(4-acetoxy-3-methoxyphenyl)acryloyloxy]-5-tert-butyldimethylsiloxy-1-hydroxycyclohexane-1,3-carbolactone; With hydrogenchloride; In tetrahydrofuran; water; at 20 ℃; for 120h; Inert atmosphere;

In tetrahydrofuran; methanol; water; Inert atmosphere; Heating;
DOI:10.1016/j.tetasy.2013.06.002

Reference yield:

: 77-95-2
D-(-)-quinic acid

: 2613-86-7
4-O-feroluoylquinic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: toluene-4-sulfonic acid / toluene; N,N-dimethyl-formamide / 18 h / Inert atmosphere; Dean-Stark; Reflux

2.1: dmap; tetra-(n-butyl)ammonium iodide; triethylamine / N,N-dimethyl-formamide / 6 h / -10 - 20 °C / Inert atmosphere

3.1: dmap; pyridine / 20 °C / Inert atmosphere

4.1: hydrogenchloride / tetrahydrofuran; water / 120 h / 20 °C / Inert atmosphere

4.2: Inert atmosphere; Heating

With pyridine; hydrogenchloride; dmap; tetra-(n-butyl)ammonium iodide; toluene-4-sulfonic acid; triethylamine; In tetrahydrofuran; water; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.tetasy.2013.06.002

Reference yield:

: 34749-55-8,147677-05-2,2596-47-6
3-(4-acetoxy-3-methoxyphenyl)prop-2-enoic acid

: 2613-86-7
4-O-feroluoylquinic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: oxalyl dichloride; N,N-dimethyl-formamide / toluene / 3 h / -5 - 10 °C / Inert atmosphere

2.1: dmap; pyridine / 20 °C / Inert atmosphere

3.1: hydrogenchloride / tetrahydrofuran; water / 120 h / 20 °C / Inert atmosphere

3.2: Inert atmosphere; Heating

With pyridine; hydrogenchloride; dmap; oxalyl dichloride; N,N-dimethyl-formamide; In tetrahydrofuran; water; toluene;
DOI:10.1016/j.tetasy.2013.06.002