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CHLOROMETHYL PHENYL SULFIDE

CHLOROMETHYL PHENYL SULFIDE ??? ???
?? ??:
7205-91-6
???:
CHLOROMETHYL PHENYL SULFIDE
???(??):
(chloromethyl)(phenyl)sulfane;(phenylthio)methyl chloride;Chlorothioanisole;α-Chlorothioanisole;ALPHA-CHLOROTHIOANISOLE;α-Chlorothioanisole >chloromethylsulfanylbenzene;[(chloromethyl)thio]benzene;CHLOROMETHYL PHENYL SULFIDE;chloromethylephenyl sulfide
CBNumber:
CB5755381
???:
C7H7ClS
??? ??:
158.65
MOL ??:
7205-91-6.mol

CHLOROMETHYL PHENYL SULFIDE ??

?? ?
66 °C/0.2 mmHg (lit.)
??
1.184 g/mL at 25 °C (lit.)
???
n20/D 1.594(lit.)
???
214 °F
?? ??
2-8°C
???
sol most organic solvents; insol H2O
??? ??
??
??
??~??? ??
??
Stench
BRN
1617369
InChI
1S/C7H7ClS/c8-6-9-7-4-2-1-3-5-7/h1-5H,6H2
InChIKey
LLSMWLJPWFSMCP-UHFFFAOYSA-N
SMILES
ClCSc1ccccc1
CAS ??????
7205-91-6(CAS DataBase Reference)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
????? 23-24/25
????(UN No.) UN 3334
WGK ?? 3
F ?????? 10-13
?? ?? ?? Stench
?? ?? 4.1
???? III
HS ?? 29309099
???? ??? 10 - Combustible liquids
???? ?? KE-05769
????(GHS): Exclamation Mark (GHS07)
?? ?: Warning
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H315 ??? ??? ??? ????? ?? ????? ?? 2 ?? P264, P280, P302+P352, P321,P332+P313, P362
H319 ?? ?? ??? ??? ?? ? ?? ?? ??? ?? ?? 2A ?? P264, P280, P305+P351+P338,P337+P313P
??????:
P264 ?? ??? ?? ??? ????.
P264 ?? ??? ?? ??? ????.
P280 ????/???/???/?????? ?????.
P302+P352 ??? ??? ??? ?? ????.
P305+P351+P338 ?? ??? ? ?? ?? ???? ????. ???? ?????? ?????. ?? ????.
P332+P313 ?? ??? ??? ???? ??· ??? ????.
P337+P313 ?? ?? ??? ???? ???? ??· ??? ????.
NFPA 704
1
0 0

CHLOROMETHYL PHENYL SULFIDE C??? ??, ??, ??

??

Reagent for the high-yield thiomethylation of O-silylated lactone and ester enolates in the synthesis of α-methylene lactones and esters.1

Synthesis

The two most convenient methods of chloromethyl phenyl sulfide are the reaction of Thioanisole with Sulfuryl Chloride and the reaction of Thiophenol with bromochloromethane using 1,8-Diazabicyclo[5.4.0]undec-7-ene or an alkali metal hydroxide as the base.

??

Chloromethyl phenyl sulfideshould be handled in a well-ventilated fume hood and kept cooled. Freshly prepared material can be stored at 0-5 °C without any appreciable decomposition. It is advisable to use freshly prepared or distilled material for reactions.

Purification Methods

Dissolve the sulfide in CH2Cl2 or CCl4 and dry it (CaCl2), or pass it through a tube of CaCl2 and distil it using a fractionating column. Harmful vapours. It gives the sulfone [7205-98-3] (b 130o/1mm and m 53o from EtOH) [Beilstein 6 IV 1507] on oxidation with permonophthalic acid. [B.hme et al. Justus Liebigs Ann Chem 563 54 64 1949.] [Beilstein 6 III 1002.]

CHLOROMETHYL PHENYL SULFIDE ?? ?? ? ???

???

?? ??


CHLOROMETHYL PHENYL SULFIDE ?? ??

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