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2-??????

2-??????
2-?????? ??? ???
?? ??:
1003-09-4
???:
2-??????
???(??):
2-??????
???:
2-Bromothiophene
???(??):
2-Bromthiophen;S0502;DKIIR;NSC 4456;INDIP-020;forTipepidine;Thienyl bromide;2-bromo-thiophen;2-BROMOTHIOPHENE;2-Bromothiaphene
CBNumber:
CB3335815
???:
C4H3BrS
??? ??:
163.04
MOL ??:
1003-09-4.mol
MSDS ??:
SDS

2-?????? ??

???
-10 °C
?? ?
149-151 °C (lit.)
??
1.684 g/mL at 25 °C (lit.)
???
n20/D 1.586(lit.)
???
140 °F
?? ??
2-8°C
??? ??
??
??
??? ??~?? ??? ??.
Specific Gravity
1.684
???
?? ? ??
??
Light Sensitive
BRN
104663
InChI
1S/C4H3BrS/c5-4-2-1-3-6-4/h1-3H
InChIKey
TUCRZHGAIRVWTI-UHFFFAOYSA-N
SMILES
Brc1cccs1
CAS ??????
1003-09-4(CAS DataBase Reference)
NIST
Thiophene, 2-bromo-(1003-09-4)
EPA
Thiophene, 2-bromo- (1003-09-4)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? T,N,Xn
?? ???? ?? 10-25-41-51/53-36/37/38-23/24-22-20/21/22
????? 26-36/37/39-45-61-16-36
????(UN No.) UN 2929 6.1/PG 2
WGK ?? 3
F ?????? 8
?? ?? ?? Irritant
TSCA TSCA listed
?? ?? 6.1
???? II
HS ?? 29349990
???? ??? 3 - Flammable liquids
Hazard Classifications Acute Tox. 2 Oral
Eye Dam. 1
Flam. Liq. 3
???? ?? KE-03715
????(GHS): Flame (GHS02)Corrosion (GHS05)Skull and Crossbones (GHS06)
?? ?: Danger
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H226 ??? ?? ? ?? ??? ?? ?? 3 ??
H300 ??? ???? ?? ?? ?? - ?? ?? 1,2 ?? P264, P270, P301+P310, P321, P330,P405, P501
H318 ?? ?? ??? ??? ?? ? ?? ?? ??? ?? ?? 1 ?? P280, P305+P351+P338, P310
??????:
P210 ?·???·??·????? ????? - ?? ???.
P233 ??? ??? ?????. ??? ??? ? ?? ?? ??? ???? ?????.
P240 ??? ????? ?? ? ??????.
P280 ????/???/???/?????? ?????.
P301+P310 ???? ?? ????(??)? ??? ????.
P305+P351+P338 ?? ??? ? ?? ?? ???? ????. ???? ?????? ?????. ?? ????.
NFPA 704
2
4 0

2-?????? MSDS


2-Bromothiophene

2-?????? C??? ??, ??, ??

??? ??

colorless to light yellow liquid. Soluble in ether and acetone, insoluble in water.

??

2-Bromothiophene has been used in electrochemical reduction of a number of mono- and dihalothiophenes at carbon cathodes in dimethylformamide containing tetramethylammonium per chlorate by cyclic voltammetry and controlled-potential electrolysis.

?? ??

2-Bromothiophene is synthesized by bromination of thiophene, which is achieved through the following steps: dissolve thiophene in acetic acid, and add bromine in glacial acetic acid solution below 10°C. Water was added to the reaction mixture to precipitate an oily liquid. Extract with ether. Add potassium carbonate to the extract to remove acetic acid, dry it, distill off the ether, and then conduct vacuum distillation to collect fractions at 42-46°C (1.73kPa) to obtain 2-bromothiophene with a yield of 55%.

?? ??

2-Bromothiophene undergoes metalation-alkylation reaction with various electrophiles to form various 5-alkylated 2-bromo products. It undergoes coupling with 4-bromo allyl phenyl ether to form allyl phenyl thiophene ether, which is a novel potential dielectric material for organic thin film transistors.

2-?????? ?? ?? ? ???

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2-?????? ?? ??:

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