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2-Thiopheneboronic acid

Product Name
2-Thiopheneboronic acid
CAS No.
6165-68-0
Chemical Name
2-Thiopheneboronic acid
Synonyms
THIOPHEN-2-YLBORONIC ACID;THIOPHENE-2-BORONIC ACID;2-THIENYLBORONIC ACID;2-thiophenylboric acid;AKOS BRN-0022;BUTTPARK 98\04-23;2-Boronothiophene;Thienylboronic aci;RARECHEM AH PB 0243;TIMTEC-BB SBB004243
CBNumber
CB6273875
Molecular Formula
C4H5BO2S
Formula Weight
127.96
MOL File
6165-68-0.mol
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2-Thiopheneboronic acid Property

Melting point:
138-140 °C (lit.)
Boiling point:
287.9±32.0 °C(Predicted)
Density 
1.32±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
Soluble in methanol.
pka
8.41±0.53(Predicted)
form 
Powder
color 
Off-white to beige
BRN 
112375
Stability:
store cold
InChI
InChI=1S/C4H5BO2S/c6-5(7)4-2-1-3-8-4/h1-3,6-7H
InChIKey
ARYHTUPFQTUBBG-UHFFFAOYSA-N
SMILES
C1(B(O)O)SC=CC=1
CAS DataBase Reference
6165-68-0(CAS DataBase Reference)
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Safety

Hazard Codes 
Xn,Xi
Risk Statements 
22-36/37/38
Safety Statements 
26-36/37-37/39-36
WGK Germany 
3
Hazard Note 
Harmful/Irritant/Keep Cold
HazardClass 
IRRITANT, IRRITANT-HARMFUL, KEEP COLD
HS Code 
29339900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
436836
Product name
2-Thienylboronic acid
Purity
≥95.0%
Packaging
1g
Price
$50.4
Updated
2025/07/31
Sigma-Aldrich
Product number
436836
Product name
2-Thienylboronic acid
Purity
≥95.0%
Packaging
5g
Price
$82.8
Updated
2025/07/31
TCI Chemical
Product number
T1772
Product name
2-Thiopheneboronic Acid (contains varying amounts of Anhydride)
Packaging
1g
Price
$23
Updated
2025/07/31
TCI Chemical
Product number
T1772
Product name
2-Thiopheneboronic Acid (contains varying amounts of Anhydride)
Packaging
5g
Price
$71
Updated
2025/07/31
Strem Chemicals
Product number
05-1040
Product name
2-Thiopheneboronic acid, min. 97%
Packaging
5g
Price
$85
Updated
2024/03/01
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2-Thiopheneboronic acid Chemical Properties,Usage,Production

Chemical Properties

white to light yellow crystal powder

Uses

suzuki reaction

Uses

2-Thienylboronic Acid is a reagent used for palladium-catalyzed Suzuki-Miyaura cross-couplings. It is also used in preparation of photophysical properties of oxygen-containing polycyclic aromatic triptycenes.

Uses

2-Thiopheneboronic acid can be used as reagent used for Palladium-catalyzed Suzuki-Miyaura cross-couplings; Alkylation, boration, coupling reaction, Suzuki coupling, and halogenation of fluorenyl bromide ;Chain-growth catalyst transfer polycondensation of conjugated alternating copolymer; Ferric perchlorate-promoted reaction of fullerene to give fullerenyl boronic esters.

Synthesis

1003-09-4

6165-68-0

General procedure for the synthesis of 2-thiophene boronic acid from 2-bromothiophene: Triphenylphosphine (0.131 g, 0.5 mmol, 20 mol%), p-iodoanisole (0.585 g, 2.5 mmol), and triethylamine (1.78 mL, 12.5 mmol) were added sequentially to a 50 mL round-bottomed flask (equipped with a side arm, condenser, and stirring bar). The reaction system was degassed three times by alternating vacuum and argon displacement. Palladium dichloride (0.023 g, 0.13 mmol, 5 mol%) was added under positive argon pressure. After stirring at room temperature for 15 minutes, diisopropylaminoborane (5 mL, 1 M THF solution, 5 mmol) was added and again degassed three times by alternating vacuum and argon displacement. The reaction mixture was heated to reflux and kept at reflux for 12 hours. Upon completion of the reaction, the mixture was cooled to 0°C and 6 mL of methanol was slowly added (note: this process is exothermic and accompanied by hydrogen release). After stirring for 15 minutes, all solvent was removed by distillation under reduced pressure to give a black solid. The solid was dissolved with 3M sodium hydroxide solution (8 mL) and subsequently washed with hexane (3 x 10 mL). The aqueous layer was cooled to 0°C (ice bath) and acidified with concentrated hydrochloric acid to pH ≤ 1, at which point 2-thiopheneboronic acid precipitated as a white solid. The aqueous layer was extracted with ether (3 x 10 mL), the organic phases were combined, dried with magnesium sulfate and filtered. Finally, the solvent was removed by distillation under reduced pressure to obtain 2-thiopheneboronic acid as a white solid.

References

[1] Tetrahedron, 2011, vol. 67, # 3, p. 576 - 583
[2] Arkiv foer Kemi, 1957, vol. 11, p. 373,379, 380
[3] New Journal of Chemistry, 2002, vol. 26, # 4, p. 373 - 375
[4] Patent: EP674635, 2001, B1

2-Thiopheneboronic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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2-Thiopheneboronic acid Suppliers

Tianjin Xinshengjiahe Technology Development Co., Ltd.
Tel
022-83719186 13212251377
Fax
086-022-8789 9925
Email
18522618860@163.com
Country
China
ProdList
79
Advantage
55
Zhuhai Aobokai Biomedical Technology Co., Ltd.
Tel
400-0628126 15697567703
Email
sales-team@aobchem.com.cn
Country
China
ProdList
49999
Advantage
58
Suzhou SuKaiLu Chemical Technology Co., Ltd.
Tel
0512-0512-62766020 15995735907
Fax
0512-62766020
Email
zwk@sukailu.com
Country
China
ProdList
956
Advantage
55
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
INTATRADE GmbH
Tel
+49 3493/605464
Fax
+49 3493/605470
Email
sales@intatrade.de
Country
Germany
ProdList
3572
Advantage
66
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Beijing HwrkChemical Technology Co., Ltd
Tel
18515581800 18501085097
Fax
010-89508210
Email
sales.bj@hwrkchemical.com
Country
China
ProdList
9400
Advantage
55
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44801
Advantage
61
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View Lastest Price from 2-Thiopheneboronic acid manufacturers

Henan Aochuang Chemical Co.,Ltd.
Product
2-Thiopheneboronic acid 6165-68-0
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
1ton
Release date
2022-10-09
Henan Fengda Chemical Co., Ltd
Product
2-Thiopheneboronic acid 6165-68-0
Price
US $8.00-6.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
g-kg-tons, free sample is available
Release date
2024-04-23
Career Henan Chemical Co
Product
2-Thiopheneboronic acid 6165-68-0
Price
US $1.00/KG
Min. Order
1G
Purity
98%
Supply Ability
1000KG
Release date
2018-08-10

6165-68-0, 2-Thiopheneboronic acidRelated Search:


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  • 6165-68-0
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  • C4H3SBOH
  • C4H3SBOH2
  • C4H5BO2S
  • Organometallic Reagents
  • Heteroaryl
  • B (Classes of Boron Compounds)
  • Boronic Acids
  • Boronic Acids and Derivatives
  • Substituted Boronic Acids
  • Boronic acids