Eugenol-d3

Base Information

Chemical Name:Eugenol-d3
CAS No.:1335401-17-6
Molecular Formula:C₁₀H₁₂O₂
Molecular Weight:167.18
Hs Code.:
Mol file:1335401-17-6.mol

Synonyms:

Suppliers and Price of Eugenol-d3

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

Usbiological
Eugenol-d3
5mg
$ 460.00

TRC
Eugenol-d3
50mg
$ 1455.00

Medical Isotopes, Inc.
Eugenol-d3
50 mg
$ 2200.00

Total 6 raw suppliers

Chemical Property of Eugenol-d3

Chemical Property:

Storage Temp.:Amber Vial, Refrigerator, Under inert atmosphere
Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly)

Purity/Quality:

99%, ^*data from raw suppliers

Eugenol-d3 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses Labelled Eugenol is a dental compound which shows cytotoxicity to human oral squamous cell carcinoma and oral cells. When glucosylated, Eugenol-d3 exhibits anti-inflammatory activity.

Technology Process of Eugenol-d3

There total 4 articles about Eugenol-d3 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: 70.0%

: 4-allyl-2-(methoxy-d₃)-phenyl 4-methylbenzenesulfonate

: 1335401-17-6
4-allyl-2-(methoxy-d₃)-phenol

Guidance literature:: With methanol; potassium hydroxide; at 20 ℃; for 1h;

Reference yield:

: 4-allyl-2-hydroxyphenyl 4-methylbenzenesulfonate

: 1335401-17-6
4-allyl-2-(methoxy-d₃)-phenol

Guidance literature:: Multi-step reaction with 2 steps

1.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0.08 h / 0 °C / Inert atmosphere

1.2: 0.5 h / 0 - 20 °C / Inert atmosphere

2.1: potassium hydroxide; methanol / 1 h / 20 °C

With methanol; di-isopropyl azodicarboxylate; triphenylphosphine; potassium hydroxide; In tetrahydrofuran; 1.2: |Mitsunobu Displacement;

Reference yield:

: 97-53-0
4-allylguaiacol

: 1335401-17-6
4-allyl-2-(methoxy-d₃)-phenol

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / dichloromethane / 0.08 h / 20 °C / Inert atmosphere

1.2: 2 h / 20 °C / Inert atmosphere

2.1: boron tribromide / dichloromethane / 4 h / -70 °C / Inert atmosphere

3.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0.08 h / 0 °C / Inert atmosphere

3.2: 0.5 h / 0 - 20 °C / Inert atmosphere

4.1: potassium hydroxide; methanol / 1 h / 20 °C

With methanol; di-isopropyl azodicarboxylate; boron tribromide; triethylamine; triphenylphosphine; potassium hydroxide; In tetrahydrofuran; dichloromethane; 3.2: |Mitsunobu Displacement;