All Photos(1)
About This Item
Linear Formula:
F2C6H3CHO
CAS Number:
Molecular Weight:
142.10
Beilstein:
1935273
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.
Recommended Products
Assay
98%
form
liquid
refractive index
n20/D 1.502 (lit.)
bp
82-84 °C/15 mmHg (lit.)
mp
15-17 °C (lit.)
density
1.317 g/mL at 25 °C (lit.)
functional group
aldehyde
fluoro
storage temp.
2-8°C
SMILES string
Fc1cccc(F)c1C=O
InChI
1S/C7H4F2O/c8-6-2-1-3-7(9)5(6)4-10/h1-4H
InChI key
SOWRUJSGHKNOKN-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Application
2,6-Difluorobenzaldehyde can be used as a reactant to synthesize:
- 5-Cyano-6-(2,6-difluorophenyl)-5,6-dihydro-2-thiouracil via one-pot cyclocondensation reaction with ethyl cyanoacetate and thiourea.[1]
- 1-(2,6-Difluorobenzyl)-2-(2,6-difluorophenyl)-benzimidazole by reacting with 1,2-phenylenediamine in the presence of a catalytic amount of p-toluenesulfonic acid.[2]
- (3E)-4-(2,6-Difluorophenyl)-3-buten-2-one by Wittig olefination reaction with acetylmethylidenetriphenyl phosphorane.[3]
- Methyl 4-fluorobenzo[b]thiophene-2-carboxylate by treating with methyl thioglycolate in the presence of K2CO3.[4]
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1C
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 2
Flash Point(F)
180.5 °F - closed cup
Flash Point(C)
82.5 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
4-Substituted (benzo [b] thiophene-2-carbonyl) guanidines as novel Na+/H+ exchanger isoform-1 (NHE-1) inhibitors
Lee Sunkyung, et al.
Bioorganic & Medicinal Chemistry Letters, 15(12), 2998-3001 (2005)
C Cabrera et al.
AIDS research and human retroviruses, 15(17), 1535-1543 (1999-12-02)
Negatively charged albumins (NCAs) have been identified as potent inhibitors of HIV-1 replication in vitro. Time of addition studies suggest that succinylated and aconitylated human serum albumin (Suc-HSA and Aco-HSA) act at an early stage of the virus life cycle
A systematic method of promoting an aryl fluoride to coordinate to ruthenium (11).
Inorgorganica Chimica Acta, 228(2), 127-131 (1995)
Some observations on the base-catalyzed cyclocondensation of 2, 6-dihalobenzaldehydes, ethyl cyanoacetate, and thiourea
Al-Omar Mohamed A, et al.
Synthetic Communications, 40(10), 1530-1538 (2010)
Microwave-assisted synthesis of benzimidazole and thiazolidinone derivatives as HIV-1 RT inhibitors
Rao Angela, et al.
ARKIVOC (Gainesville, FL, United States), 5, 147-155 (2004)
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
