1,4-Naphthalenedione, 2-ethyl-3-hydroxy-

Base Information

Chemical Name:1,4-Naphthalenedione, 2-ethyl-3-hydroxy-
CAS No.:29366-44-7
Molecular Formula:C12H10 O3
Molecular Weight:202.21
Hs Code.:2914690090
NSC Number:108022
DSSTox Substance ID:DTXSID20951909
Nikkaji Number:J99.679C
ChEMBL ID:CHEMBL3092105
Mol file:29366-44-7.mol

Synonyms:29366-44-7;1,4-Naphthalenedione, 2-ethyl-3-hydroxy-;3-ethyl-4-hydroxynaphthalene-1,2-dione;2-ETHYL-3-HYDROXYNAPHTHALENE-1,4-DIONE;NSC108022;2-Ethyl-3-hydroxy-1,4-naphthoquinone;1,4-Naphthoquinone, 2-ethyl-3-hydroxy-;1, 2-ethyl-3-hydroxy-;Cambridge id 5249318;Oprea1_408438;SCHEMBL8781044;CHEMBL3092105;DTXSID20951909;VVAZSPXIJHYPKY-UHFFFAOYSA-N;2-Ethyl-3-hydroxynaphthoquinone #;2-hydroxy-3-ethyl-1,4-naphthoquinone;NSC 108022;NSC-108022;SR-01000200918;SR-01000200918-1

Suppliers and Price of 1,4-Naphthalenedione, 2-ethyl-3-hydroxy-

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 4 raw suppliers

Chemical Property of 1,4-Naphthalenedione, 2-ethyl-3-hydroxy-

Chemical Property:

Vapor Pressure:6.32E-06mmHg at 25°C
Boiling Point:363.7°Cat760mmHg
Flash Point:187.9°C
PSA：54.37000
Density:1.32g/cm³
LogP:2.28770
XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:202.062994177
Heavy Atom Count:15
Complexity:341

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1=C(C2=CC=CC=C2C(=O)C1=O)O

Technology Process of 1,4-Naphthalenedione, 2-ethyl-3-hydroxy-

There total 28 articles about 1,4-Naphthalenedione, 2-ethyl-3-hydroxy- 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: 90.0%

: (5S,6R,8S)-6-acetyl-8-ethyl-5-hydroxy-7,8-dihydro-5H-5,8-methanobenzo[7]annulene-9,10(6H)-dione

: 29366-44-7
2-ethyl-3-hydroxy-[1,4]naphthoquinone

Guidance literature:: With potassium tert-butylate; at 20 ℃; for 1h; Inert atmosphere;
DOI:10.1002/anie.201706557

Reference yield: 80.0%

: 27699-93-0
2‐hydroxy‐1,4‐naphthoquinone

: 75-07-0,9002-91-9
acetaldehyde

: 29366-44-7
2-ethyl-3-hydroxy-[1,4]naphthoquinone

Guidance literature:: With diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; L-proline; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1002/anie.201706557