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2,3-Difluorotoluene

2,3-Difluorotoluene Suppliers list
Company Name: Shanghai Harvest Chemical Industrial Co., Ltd.  Gold
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Company Name: SHAANXI DIDEU MEDICHEM CO.LTD  Gold
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Company Name: Hubei xingongli Chemical Co., Ltd  Gold
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Company Name: Shijiazhuang Smao Chemical Technology Co., Ltd  Gold
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Company Name: J & K SCIENTIFIC LTD.  
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2,3-Difluorotoluene manufacturers

  • 2,3-Difluorotoluene
  • 2,3-Difluorotoluene pictures
  • $1.00
  • 2024-07-16
  • CAS:3828-49-7
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 20t
2,3-Difluorotoluene Basic information
Product Name:2,3-Difluorotoluene
Synonyms:Difluorotoluene 23-;2, 3 - two fluorine toluene;2,3-DIFLUOROTOLUENE;1,2-DIFLUORO-3-METHYL-BENZENE;Difluorotoluene1;2,3-difluoromethylbenzene;2,3-Difluorotoluene, 97+%;2,3-Difluorotoluene,96%
CAS:3828-49-7
MF:C7H6F2
MW:128.12
EINECS:000-000-0
Product Categories:Fluorin-contained toluene series;Halogen toluene;Miscellaneous;Aryl;C7;Halogenated Hydrocarbons;Fluorobenzene;bc0001
Mol File:3828-49-7.mol
2,3-Difluorotoluene Structure
2,3-Difluorotoluene Chemical Properties
Boiling point 119-121 °C (lit.)
density 1.096 g/mL at 25 °C (lit.)
refractive index n20/D 1.4530(lit.)
Fp 15°C
storage temp. Sealed in dry,Room Temperature
solubility 0.24g/l
form liquid
color Clear, faint lemon/lime
Specific Gravity1.120
BRN 3235341
InChIInChI=1S/C7H6F2/c1-5-3-2-4-6(8)7(5)9/h2-4H,1H3
InChIKeyZNEHIDGAPGVZSA-UHFFFAOYSA-N
SMILESC1(F)=CC=CC(C)=C1F
CAS DataBase Reference3828-49-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,F
Risk Statements 10-22-37/38-41
Safety Statements 16-26-39
RIDADR UN 1993 3/PG 2
WGK Germany 2
Hazard Note Flammable
HazardClass 3
PackingGroup II
HS Code 29039990
Storage Class3 - Flammable liquids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Dam. 1
Flam. Liq. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
1,2-Difluoro-3-methylbenzene English
SigmaAldrich English
ALFA English
2,3-Difluorotoluene Usage And Synthesis
Chemical Propertiescolorless to light yellow liqui
Uses2,3-Difluorotoluene serves as an intermediate for the synthesis of pharmaceuticals, electronics and agrochemical products [1].
References[1] Power, M., Alcock, E., McGlacken*, G. P. (2020). Organolithium Bases in Flow Chemistry: A Review. Organic Process Research Development, 24 10, 1814–1838. https://doi.org/10.1021/acs.oprd.0c00090
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