4701-17-1
- Product Name：5-Bromothiophene-2-carbaldehyde
- Molecular Formula：C5H3BrOS
- Purity：99%
- Molecular Weight：191.048
Product Details;
CasNo： 4701-17-1
Molecular Formula： C5H3BrOS
Appearance： clear yellow to brown liquid after melting
factory and supplier 4701-17-1 5-Bromothiophene-2-carbaldehyde in stock
- Molecular Formula:C5H3BrOS
- Molecular Weight:191.048
- Appearance/Colour:clear yellow to brown liquid after melting
- Vapor Pressure:0.065mmHg at 25°C
- Melting Point:104-6ºC
- Refractive Index:n20/D 1.637(lit.)
- Boiling Point:230.687 °C at 760 mmHg
- Flash Point:98.889 °C
- PSA：45.31000
- Density:1.789 g/cm3
- LogP:2.32310
5-Bromothiophene-2-carbaldehyde(Cas 4701-17-1) Usage
|
Synthesis Reference(s) |
Journal of the American Chemical Society, 72, p. 1422, 1950 DOI: 10.1021/ja01159a527 |
InChI:InChI=1/C5H3BrOS/c6-5-2-1-4(3-7)8-5/h1-3H
4701-17-1 Relevant articles
Synthesis and characterization of 5′-hexyl-2,2′-bithiophene based on organic dyes for dye-sensitized solar cell applications
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, p. 157 - 162 (2014)
A series of new organic dyes, 2-(2,6-bis...
Frequency and electric field controllable photodevice: FYTRONIX device
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, p. 53 - 58 (2017)
Al/p-Si/BODIPY/Al diode was fabricated b...
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, p. 11457 - 11464 (2019)
We designed and synthesized four donor-a...
Cerium-photocatalyzed aerobic oxidation of benzylic alcohols to aldehydes and ketones
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supporting information, p. 1727 - 1732 (2021/08/05)
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Direct bromodeboronation of arylboronic acids with CuBr2 in water
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SUBSTITUTED 1H-IMIDAZO[4,5-B]PYRIDIN-2(3H)-ONES AND THEIR USE AS GLUN2B RECEPTOR MODULATORS
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Page/Page column 134; 135, (2018/04/23)
Substituted 1 H-imidazo[4,5-b]pyridin-2(...
4701-17-1 Process route
-
-
98-03-3
thiophene-2-carbaldehyde
-
-
4701-17-1
5-bromo-2-thiophencarboxaldehyde
| Conditions | Yield |
|---|---|
|
With
N-Bromosuccinimide;
In
chloroform;
at 20 ℃;
|
98% |
|
With
bromine; sodium hydrogencarbonate;
In
chloroform;
at 20 ℃;
for 2h;
|
80% |
|
With
pyridinium hydrobromide perbromide; orthoformic acid triethyl ester;
In
1,2-dichloro-ethane;
at 50 ℃;
for 2h;
|
73% |
|
With
acetic acid;
In
chloroform;
at 0 - 20 ℃;
for 13h;
Darkness;
|
35% |
|
With
chloroform; bromine;
|
|
|
With
bromine;
|
|
|
With
bromine; sodium hydrogencarbonate;
In
chloroform;
|
|
|
With
N-Bromosuccinimide;
In
N,N-dimethyl-formamide;
|
|
|
With
bromine; sodium hydrogencarbonate;
In
chloroform;
|
-
-
79387-71-6
(5-bromothien-2-yl)methanol
-
-
4701-17-1
5-bromo-2-thiophencarboxaldehyde
| Conditions | Yield |
|---|---|
|
With
cerium(III) chloride heptahydrate; sodium hydrogencarbonate;
In
acetonitrile;
at 50 ℃;
for 35h;
Irradiation;
Sealed tube;
|
80% |
|
With
Candida parapsilosis ATCC 7330;
In
hexane; water;
at 25 ℃;
for 24h;
Green chemistry;
Enzymatic reaction;
|
77% |
|
With
iron(III) chloride hexahydrate; C17H26N3(1+)*Br(1-); dihydrogen peroxide;
In
water;
at 20 ℃;
for 3h;
chemoselective reaction;
|
77% |
4701-17-1 Upstream products
-
1003-09-4
2-bromothiophene
-
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N,N-dimethyl-formamide
-
93-61-8
N-methyl-N-phenylformamide
-
98-03-3
thiophene-2-carbaldehyde
4701-17-1 Downstream products
-
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-
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-
96463-58-0
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-
81020-73-7
3c-(5-bromo-[2]thienyl)-2-phenyl-acrylonitrile
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