2,6-Difluorobenzoyl chloride

2,6-Difluorobenzoyl chloride Basic information
Product Name:2,6-Difluorobenzoyl chloride
Synonyms:Benzoyl chloride, 2,6-difluoro-;PYROMUCIC ACID;RARECHEM AL BO 0190;TIMTEC-BB SBB004324;TIMTEC-BB SBB006739;LABOTEST-BB LTBB000722;FUROIC ACID;FAC
CAS:18063-02-0
MF:C7H3ClF2O
MW:176.55
EINECS:241-971-2
Product Categories:Miscellaneous;Acid Halides;Carbonyl Compounds;Organic Building Blocks
Mol File:18063-02-0.mol
2,6-Difluorobenzoyl chloride Structure
2,6-Difluorobenzoyl chloride Chemical Properties
Melting point 128-132 °C(lit.)
Boiling point 72-77 °C/13 mmHg (lit.)
density 1.404 g/mL at 25 °C (lit.)
refractive index n20/D 1.501(lit.)
Fp 121 °F
storage temp. Inert atmosphere,Room Temperature
form clear liquid
color Colorless to Light orange to Yellow
Specific Gravity1.404
Water Solubility REACTS
Sensitive Moisture Sensitive
BRN 639438
CAS DataBase Reference18063-02-0(CAS DataBase Reference)
NIST Chemistry Reference2,6-Difluorobenzoyl chloride(18063-02-0)
Safety Information
Hazard Codes C
Risk Statements 36/37/38-34-10
Safety Statements 26-36/37/39-45-28A-16
RIDADR UN 2920 8/PG 2
WGK Germany 3
RTECS LV1763000
21
Hazard Note Corrosive
HazardClass 8
PackingGroup II
HS Code 29163990
MSDS Information
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2,6-Difluorobenzoyl chloride Usage And Synthesis
Chemical PropertiesCLEAR COLOURLESS TO LIGHT YELLOW LIQUID
Uses2,6-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
UsesPreservative, bactericide, furoates for perfume and flavoring, fumigant, textile processing, chemical intermediate.
2,6-Difluorobenzoyl chloride Preparation Products And Raw materials
Preparation Products2,6-Difluorobenzoyl isocyanate-->BenzaMide, 2,6-difluoro-N-(4-iodophenyl)-->2,6-Difluoro-N-phenylbenzamide, 97%-->2,6-Difluoro-N-methyl-N-phenylbenzamide, 97%-->2,6-Difluoro-N-(3-chloro-4-methylphenyl)benzamide, 97%-->2,6-Difluoro-N-methoxy-N-methylbenzamide-->Methanone, (2,6-difluorophenyl)(4-fluorophenyl)--->2,6-Difluoro-N-(4-Methoxyphenyl)benzaMide, 97%-->2-ACETOXY-2',6'-DIFLUOROBENZOPHENONE
3,5-Dichloro-2,4-difluorobenzoyl chloride 5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-2-FUROIC ACID 5-[(4-CHLOROPHENOXY)METHYL]-2-FUROIC ACID 5-[3-(TRIFLUOROMETHOXY)PHENYL]-2-FUROIC ACID 5-(4-CHLORO-3-FLUOROPHENYL)-2-FUROIC ACID 5-[(4-FLUOROPHENOXY)METHYL]-2-FUROIC ACID 5-(4-ACETYLPHENYL)-2-FUROIC ACID 5-[(4-ETHYLPHENOXY)METHYL]-2-FUROIC ACID 5-[(3-TERT-BUTYLPHENOXY)METHYL]-2-FUROIC ACID 2,6-DIFLUORO-3-NITROBENZOYL CHLORIDE 5-[4-(BENZYLOXY)PHENYL]-2-FUROIC ACID 4-CHLORO-2,6-DIFLUOROBENZOYL CHLORIDE 5-[(4-CHLORO-1H-PYRAZOL-1-YL)METHYL]-2-FUROIC ACID 5-(4-BROMOPHENYL)-2-(TRIFLUOROMETHYL)-3-FUROIC ACID 5-[3-(TRIFLUOROMETHYL)PHENYL]-2-FUROIC ACID 5-[(4-CHLORO-2-METHYLPHENOXY)METHYL]-2-FUROIC ACID 5-[4-(ETHOXYCARBONYL)PHENYL]-2-FUROIC ACID 5-([4-[(E)-2-CARBOXYVINYL]-2-METHOXYPHENOXY]METHYL)-2-FUROIC ACID

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