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2-Fluoroethyl4-methylbenzenesulfonate

2-Fluoroethyl4-methylbenzenesulfonate structure

2-Fluoroethyl4-methylbenzenesulfonate 

structure
  • CAS No:

    383-50-6

  • Formula:

    C9H11FO3S

  • Chemical Name:

    2-Fluoroethyl4-methylbenzenesulfonate

  • Synonyms:

    Fluoroethylp-tosylate;2-FLUOROETHYLTOSYLATE;L-TRYPTOPHAN/D-TRYPTOPHAN;FLUOROETHYL4-TOLUENESULFONATE;Fluoroethylp-toluenesulfonate;2-fluoroethyl4-methylbenzenesulfonate;2-fluoroethyl4-Methylbenzene-1-sulfonate;2-Fluoro-(4-methylbenzenesulfonate)ethanol;4-Methylbenzenesulfonicacid2-fluoro-ethylester

  • Categories:

    Chemical Reagents  >  Organic Reagents

2-Fluoroethyl4-methylbenzenesulfonate Basic Attributes

218.25

218.04100

82210

DTXSID80292385

2905590090

Characteristics

51.8

1.8

colorless or light-yellow liquid

1.241 g/cm3

140°C/1mmHg(lit.)

156.4ºC

1.495

Safety Information

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, and P362|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Drug Information

(3H)fluoroethyl tosylate

2-Fluoroethyl4-methylbenzenesulfonate Use and Manufacturing

Methods of Manufacturing

From the reaction of fluoroethanol and p-toluenesulfonyl chloride. Mix 29.5g 2-fluoroethanol (0.46mol) with 97.2g p-toluenesulfonyl chloride (0.51mol), and add 74.4ml pyridine dropwise at -7°C. Keep -5-0 ℃ dripping and continue the reaction for 2h to obtain 81.8 g of fluoroethyl p-toluenesulfonate. The yield was 81.5%.

Uses

Intermediate of fleroxacin.

Computed Properties

Molecular Weight:218.25
XLogP3:1.8
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:218.04129354
Monoisotopic Mass:218.04129354
Topological Polar Surface Area:51.8
Heavy Atom Count:14
Complexity:250
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Material

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