3-(Trifluoromethyl)benzaldehyde

Base Information Edit

Chemical Name:3-(Trifluoromethyl)benzaldehyde
CAS No.:454-89-7
Molecular Formula:C8H5F3O
Molecular Weight:174.122
Hs Code.:29130000
European Community (EC) Number:207-228-1
UNII:AT7H4H5U3E
DSSTox Substance ID:DTXSID8022032
Nikkaji Number:J60.109H
Wikidata:Q27274112
ChEMBL ID:CHEMBL4561632
Mol file:454-89-7.mol

Synonyms:3-(Trifluoromethyl)benzaldehyde;454-89-7;3-Trifluoromethylbenzaldehyde;Benzaldehyde, 3-(trifluoromethyl)-;m-Trifluoromethylbenzaldehyde;alpha,alpha,alpha-Trifluoro-m-tolualdehyde;a,a,a-trifluoro-m-tolualdehyde;m-(trifluoromethyl)benzaldehyde;alpha,alpha,alpha-Trifluoro-3-tolualdehyde;MFCD00003373;3-(trifluoromethyl)-benzaldehyde;EINECS 207-228-1;UNII-AT7H4H5U3E;AT7H4H5U3E;3-(trifluoromethyl) benzaldehyde;m-Tolualdehyde, .alpha.,.alpha.,.alpha.-trifluoro-;alpha, alpha, alpha-Trifluoro-m-tolualdehyde;m-trifluoromethylbezaldehyde;3-trifluormethylbenzaldehyde;3-trifluoromethy-benzaldehyde;SCHEMBL67201;m-trifluoromethyl benzaldehyde;3-trifluoromethyl-benzaldehyde;3-Trifluoromethyl benzaldehyde;meta-trifluoromethylbenzaldehyde;CHEMBL4561632;DTXSID8022032;m-(trifluoromethyl) benzaldehyde;3- (trifluoromethyl)benzaldehyde;CS-M1039;STK505660;3-(trifluoromethyl)benzenecarbaldehyde;3-(Trifluoromethyl)benzaldehyde, 97%;AKOS000321287;AC-3866;PS-8632;HY-76574;LS-184877;A7162;AM20060044;FT-0613919;I+/-,I+/-,I+/--trifluoro-3-tolualdehyde;T1399;3-(TRIFLUOROMETHYL)PHENYLCARBOXALDEHYDE;EN300-21347;D77401;.alpha. .alpha. .alpha.-Trifluoro-m-tolualdehyde;W-106135;Q27274112;F2190-0731;Z104495494

Suppliers and Price of 3-(Trifluoromethyl)benzaldehyde

Supply Marketing:Edit

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
3-(Trifluoromethyl)benzaldehyde
25g
$ 65.00

TCI Chemical
3-(Trifluoromethyl)benzaldehyde >95.0%(GC)
5g
$ 40.00

TCI Chemical
3-(Trifluoromethyl)benzaldehyde >95.0%(GC)
25g
$ 116.00

SynQuest Laboratories
3-(Trifluoromethyl)benzaldehyde 98%
250 g
$ 80.00

SynQuest Laboratories
3-(Trifluoromethyl)benzaldehyde 98%
1 kg
$ 300.00

SynQuest Laboratories
3-(Trifluoromethyl)benzaldehyde 98%
100 g
$ 35.00

SynQuest Laboratories
3-(Trifluoromethyl)benzaldehyde 98%
50 g
$ 20.00

Sigma-Aldrich
3-(Trifluoromethyl)benzaldehyde 97%
25g
$ 76.60

Sigma-Aldrich
3-(Trifluoromethyl)benzaldehyde 97%
5g
$ 52.00

Medical Isotopes, Inc.
3-(Trifluoromethyl)benzaldehyde
50 g
$ 610.00

Total 160 raw suppliers

Chemical Property of 3-(Trifluoromethyl)benzaldehyde Edit

Chemical Property:

Appearance/Colour:clear very slight orange
Vapor Pressure:3.05mmHg at 25°C
Refractive Index:n20/D 1.465(lit.)
Boiling Point:176.3 °C at 760 mmHg
Flash Point:68.3 °C
PSA：17.07000
Density:1.293 g/cm³
LogP:2.51790
Storage Temp.:Keep in dark place,Sealed in dry,Room Temperature
Sensitive.:Air Sensitive
XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:174.02924926
Heavy Atom Count:12
Complexity:164

Purity/Quality:

99% ^*data from raw suppliers

3-(Trifluoromethyl)benzaldehyde ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:C1=CC(=CC(=C1)C(F)(F)F)C=O
Uses 3-(Trifluoromethyl)benzaldehyde is used as a reagent in the synthesis of 2,3-di- and 2,2,3-trisubstituted-3-methoxycarbonyl-γ-butyrolactones as potent antitumor agents. Also used as a reagent in the synthesis of novel chalcone derivatives as hypoxia-inducible factor (HIF)-1 inhibitors.

Technology Process of 3-(Trifluoromethyl)benzaldehyde

There total 48 articles about 3-(Trifluoromethyl)benzaldehyde 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: 100.0%