Endiandric acid A

Base Information

Chemical Name:Endiandric acid A
CAS No.:74591-03-0
Molecular Formula:C21H22O2
Molecular Weight:306.404
Hs Code.:
UNII:84CSS3T9ZC
Nikkaji Number:J859.158J
Wikidata:Q27269519

Synonyms:Endiandric acid A;Endiandric acid A [MI];Endiandric acid A, (+/-)-;UNII-84CSS3T9ZC;84CSS3T9ZC;74591-03-0;1H-Cyclobut(bc)acenaphthylene-1-acetic acid, 1a,2,2a,5,5a,7a,7b,7c-octahydro-5-phenyl-, (1R,1aR,2aR,5S,5aS,7aS,7bR,7cr)-rel-;Rel-(1R,1aR,2aR,5S,5aS,7aS,7bR,7cr)-1a,2,2a,5,5a,7a,7b,7c-octahydro-5-phenyl-1H-cyclobut(bc)acenaphthylene-1-acetic acid;SCHEMBL5881331;Q27269519

Suppliers and Price of Endiandric acid A

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

American Custom Chemicals Corporation
ENDIANDRIC ACID A 95.00%
5MG
$ 495.96

Total 1 raw suppliers

Chemical Property of Endiandric acid A

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Melting Point:147-149°
Boiling Point:476.8°Cat760mmHg
PKA:5.1, 5.0(at 25℃)
Flash Point:373.4°C
PSA：37.30000
Density:1.193g/cm³
LogP:4.11520
XLogP3:4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:306.161979940
Heavy Atom Count:23
Complexity:556

Purity/Quality:

98% ^*data from raw suppliers

ENDIANDRIC ACID A 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C2C=CC(C3C2C4C1C(C4C=C3)CC(=O)O)C5=CC=CC=C5
Isomeric SMILES:C1[C@H]2C=C[C@H]([C@H]3[C@@H]2[C@H]4[C@@H]1[C@@H]([C@H]4C=C3)CC(=O)O)C5=CC=CC=C5

Technology Process of Endiandric acid A

There total 26 articles about Endiandric acid A 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: 95.0%

: 82679-80-9
((1S,1aS,2aS,5R,5aR,7aR,7bS,7cS)-5-Phenyl-1a,2,2a,5,5a,7a,7b,7c-octahydro-1H-cyclobuta[bc]acenaphthylen-1-yl)-acetonitrile

: 74591-03-0
(±)-endiandric acid A

Guidance literature:: With potassium hydroxide; dihydrogen peroxide; In ethanol; water; 25 deg C -> 50 deg C;
DOI:10.1021/ja00384a077

Reference yield: 86.0%

: 2-(6'-phenyltetracyclo<5,4,2,0^3,13,0^10,12>trideca-4',8'-dien-11'-yl)ethanol

: 74591-03-0
(±)-endiandric acid A

Guidance literature:: With tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide; In water; acetonitrile;
DOI:10.1039/c5sc00794a

Reference yield:

: 82679-79-6
(1S,1aR,2aS,5R,5aR,7aS,7bS,7cS)-1-Bromomethyl-5-phenyl-1a,2,2a,5,5a,7a,7b,7c-octahydro-1H-cyclobuta[bc]acenaphthylene

: 74591-03-0
(±)-endiandric acid A

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / hexamethylphosphoric acid triamide / 25 °C

2: 95 percent / KOH, H₂O₂ / H₂O; ethanol / 25 deg C -> 50 deg C

With potassium hydroxide; dihydrogen peroxide; In N,N,N,N,N,N-hexamethylphosphoric triamide; ethanol; water;
DOI:10.1021/ja00384a077