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249408

Sigma-Aldrich

2,6-Difluorobenzoyl chloride

99%

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About This Item

Linear Formula:
F2C6H3COCl
CAS Number:
18063-02-0
Molecular Weight:
176.55
Beilstein:
639438
EC Number:
241-971-2
MDL number:
MFCD00000659
UNSPSC Code:
12352100
PubChem Substance ID:
24854989

Assay

99%

form

liquid

refractive index

n20/D 1.501 (lit.)

bp

72-77 °C/13 mmHg (lit.)

density

1.404 g/mL at 25 °C (lit.)

SMILES string

Fc1cccc(F)c1C(Cl)=O

InChI

1S/C7H3ClF2O/c8-7(11)6-4(9)2-1-3-5(6)10/h1-3H

InChI key

QRHUZEVERIHEPT-UHFFFAOYSA-N

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Application

2,6-Difluorobenzoyl chloride has been used in:
  • the preparation of series of novel 2-aryl substituted 4H-3,1-benzoxazin-4-ones
  • regioselective synthesis of 3,6-disubstituted-2-aminoimidazo[1,2-a]pyridine
  • Friedel-Crafts acylation reaction of toluene, anisol, thioanisol, 4-phenoxyacetophenone and N,N-diacetyl-4-phenoxyaniline

Pictograms

FlameCorrosion
GHS02,GHS05

Signal Word

Danger

Hazard Statements

H226,H314

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

114.8 °F - closed cup

Flash Point(C)

46 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

249408-5G:
249408-100G:
249408-25G:
249408-BULK:
249408-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCG2082
MKBS6908V
MKBR3930V
MKBM4808V
MKBL6334V

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P Jakobsen et al.
Bioorganic & medicinal chemistry, 8(8), 2095-2103 (2000-09-26)
The synthesis of a series of novel 2-aryl substituted 4H-3,1-benzoxazin-4-ones and their evaluation as specific inhibitors of the Tissue Factor (TF)/Factor VIIa (FVIIa)-induced pathway of coagulation is reported. Inhibitory activities (IC50 values) in the range 0.17 to > 40 microM
New polymer syntheses, 36. Functionalized aromatic polyethers derived from 4'-substituted 2, 6-difluorobenzophenones.
Kricheldorf HR and Delius U.
Makromol. Chem., 190(6), 1277-1288 (1989)
Regioselective synthesis of 3, 6-disubstituted-2-aminoimidazo [1, 2-a] pyridines.
Jaramillo C, et al.
Tetrahedron Letters, 43(50), 9051-9054 (2002)

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