4-Fluoro-1-naphthaldehyde

Base Information

Chemical Name:4-Fluoro-1-naphthaldehyde
CAS No.:172033-73-7
Molecular Formula:C11H7FO
Molecular Weight:174.174
Hs Code.:2913000090
European Community (EC) Number:622-655-7
DSSTox Substance ID:DTXSID90427449
Nikkaji Number:J688.752J
Wikidata:Q72475069
ChEMBL ID:CHEMBL4449111
Mol file:172033-73-7.mol

Synonyms:4-fluoro-1-naphthaldehyde;172033-73-7;4-fluoronaphthalene-1-carbaldehyde;1-Naphthalenecarboxaldehyde, 4-fluoro-;4-FLUORO-1-NAPHTHALENECARBOXALDEHYDE;MFCD02261765;4-fluoro-naphthalene-1-carbaldehyde;4-Fluoronaphthalene-1-carboxaldehyde;SCHEMBL485577;CHEMBL4449111;AMY7798;DTXSID90427449;LZUCGZVKZDBILP-UHFFFAOYSA-N;4-Fluoro-1-naphthaldehyde, 97%;4-fluoro-1-naphthalenecarbaldehyde;STK894027;AKOS005638663;CS-W017508;AC-33889;AS-11118;SY046821;FT-0668688;EN300-126056;J-010789;Z1162445938

Suppliers and Price of 4-Fluoro-1-naphthaldehyde

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

AK Scientific
4-Fluoro-1-naphthaldehyde
1g
$ 93.00

Alichem
4-Fluoro-1-naphthaldehyde
1g
$ 159.39

Alichem
4-Fluoro-1-naphthaldehyde
5g
$ 527.56

American Custom Chemicals Corporation
4-FLUORO-1-NAPHTHALENECARBOXALDEHYDE 95.00%
500MG
$ 750.75

American Custom Chemicals Corporation
4-FLUORO-1-NAPHTHALENECARBOXALDEHYDE 95.00%
5G
$ 2136.75

AOBChem
4-Fluoro-1-naphthaldehyde 97%
500mg
$ 59.00

Apolloscientific
4-Fluoro-1-naphthaldehyde 95+%
1g
$ 209.00

Apolloscientific
4-Fluoro-1-naphthaldehyde 95+%
5g
$ 517.00

TRC
4-Fluoro-1-naphthaldehyde
1g
$ 110.00

SynQuest Laboratories
4-Fluoro-1-naphthaldehyde
25 g
$ 1480.00

Total 39 raw suppliers

Chemical Property of 4-Fluoro-1-naphthaldehyde

Chemical Property:

Vapor Pressure:0.000706mmHg at 25°C
Melting Point:79-81oC
Boiling Point:307.9oC at 760 mmHg
Flash Point:198.7oC
PSA：17.07000
Density:1.249g/cm3
LogP:2.79140
Storage Temp.:under inert gas (nitrogen or Argon) at 2-8°C
Solubility.:DMSO (Slightly), Methanol (Slightly)
XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:174.048093005
Heavy Atom Count:13
Complexity:193

Purity/Quality:

97% ^*data from raw suppliers

4-Fluoro-1-naphthaldehyde ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Statements: 52/53
Safety Statements: 61

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C(=CC=C2F)C=O
Uses 4-Fluoro-1-naphthaldehyde (cas# 172033-73-7) is a compound useful in organic synthesis.

Technology Process of 4-Fluoro-1-naphthaldehyde

There total 4 articles about 4-Fluoro-1-naphthaldehyde 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: 93.0%

: 4885-02-3
Dichloromethyl methyl ether

: 321-38-0
1-Fluoronaphthalene

: 172033-73-7
4-fluoro-1-naphthalenecarbaldehyde

Guidance literature:: With tin(IV) chloride; In dichloromethane; 0 deg C to room temperature;
DOI:10.1021/jo00125a055

Reference yield: 52.0%

: 341-41-3
1-bromo-4-fluoronaphthalene

: 68-12-2,33513-42-7
N,N-dimethyl-formamide

: 172033-73-7
4-fluoro-1-naphthalenecarbaldehyde

Guidance literature:: 1-bromo-4-fluoronaphthalene; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 2h; Inert atmosphere;

N,N-dimethyl-formamide; In tetrahydrofuran; at -78 ℃; Inert atmosphere;
DOI:10.1055/s-0039-1690718

Reference yield: 50.0%

: 42758-54-3
4-nitro-1-naphthaldehyde

: 172033-73-7
4-fluoro-1-naphthalenecarbaldehyde

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; for 0.166667h; Inert atmosphere; Microwave irradiation;
DOI:10.1016/j.tetlet.2010.02.042