4-(Naphthalen-1-yl)benzoic acid

Base Information

Chemical Name:4-(Naphthalen-1-yl)benzoic acid
CAS No.:106359-69-7
Molecular Formula:C17H12 O2
Molecular Weight:248.281
Hs Code.:2916399090
European Community (EC) Number:673-788-2
DSSTox Substance ID:DTXSID40375042
Nikkaji Number:J344.150D
Wikidata:Q82163585
Mol file:106359-69-7.mol

Synonyms:4-(Naphthalen-1-yl)benzoic acid;106359-69-7;4-naphthalen-1-ylbenzoic Acid;4-Naphthalen-1-yl-benzoic acid;4-(1-Naphthyl)benzoic acid;4-(2-HYDROXYNAPHTHALEN-1-YL)BENZOIC ACID;4-(Naphthalen-1-yl)benzoicacid;SCHEMBL5788498;DTXSID40375042;MFCD04117438;AKOS005816552;FS-6477;4-(4-AMINONAPHTHALEN-1-YL)BENZOIC ACID

Suppliers and Price of 4-(Naphthalen-1-yl)benzoic 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

TRC
4-Naphthalen-1-yl-benzoicAcid
100mg
$ 130.00

Crysdot
4-(Naphthalen-1-yl)benzoicacid 95+%
5g
$ 847.00

Chemenu
4-(naphthalen-1-yl)benzoicacid 95%
5g
$ 800.00

American Custom Chemicals Corporation
4-NAPHTHALEN-1-YL-BENZOIC ACID 98.00%
0.5G
$ 1334.30

Alichem
4-(Naphthalen-1-yl)benzoicacid
250mg
$ 494.40

AK Scientific
4-(Naphthalen-1-yl)benzoicacid
5g
$ 1251.00

Total 10 raw suppliers

Chemical Property of 4-(Naphthalen-1-yl)benzoic acid

Chemical Property:

PSA：37.30000
LogP:4.20500
Storage Temp.:2-8°C
XLogP3:4.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:248.083729621
Heavy Atom Count:19
Complexity:317

Purity/Quality:

97% ^*data from raw suppliers

4-Naphthalen-1-yl-benzoicAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=CC=C2C3=CC=C(C=C3)C(=O)O

Technology Process of 4-(Naphthalen-1-yl)benzoic acid

There total 13 articles about 4-(Naphthalen-1-yl)benzoic 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: 97.0%

: 586-76-5
4-Bromobenzoic acid

: 7029-32-5
dinaphthalen-1-ylzinc

: 106359-69-7
4-(naphthalen-1-yl)benzoic acid

Guidance literature:: With dichloro{bis[1-(dicyclohexylphosphanyl)piperidine]}palladium(II); In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; at 100 ℃; for 0.0833333h; In air;
DOI:10.1002/chem.201001201

Reference yield: 88.0%

: 619-58-9
4-iodobenzoic acid

: 13922-41-3
1-Naphthylboronic acid

: 106359-69-7
4-(naphthalen-1-yl)benzoic acid

Guidance literature:: With potassium phosphate tribasic trihydrate; In tetrahydrofuran; water; for 6h; Reflux;
DOI:10.1002/ejoc.201101749

Reference yield: 84.0%

: 586-76-5
4-Bromobenzoic acid

: 703-55-9
1-naphthylmagnesiumbromide

: 106359-69-7
4-(naphthalen-1-yl)benzoic acid

Guidance literature:: 1-naphthylmagnesiumbromide; With titanium(IV) tetraethanolate; In tetrahydrofuran; at 20 ℃; for 0.5h; Inert atmosphere;

4-Bromobenzoic acid; With tributylphosphine; cobalt(II) chloride; In tetrahydrofuran; at 20 ℃; chemoselective reaction; Inert atmosphere;
DOI:10.1021/ol402599f