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3-Thiopheneboronic acid

CAS No.
6165-69-1
Chemical Name:
3-Thiopheneboronic acid
Synonyms
THIOPHEN-3-YLBORONIC ACID;THIOPHENE-3-BORONIC ACID;AKOS BRN-0047;3-thienoborate;3-Boronothiophene;TIMTEC-BB SBB004244;RARECHEM AH PB 0232;3-Thiopheneboronica;3-ThiopheneBoricAcid;3-THIENYLBORONIC ACID
CBNumber:
CB2755805
Molecular Formula:
C4H5BO2S
Molecular Weight:
127.96
MDL Number:
MFCD00151851
MOL File:
6165-69-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 14:58:10
Product description Number Pack Size Price
3-Thienylboronic acid ≥95.0% 436844 1g $40
3-Thienylboronic acid ≥95.0% 436844 5g $81.1
3-Thiopheneboronic Acid (contains varying amounts of Anhydride) T1975 1g $30
3-Thiopheneboronic Acid (contains varying amounts of Anhydride) T1975 5g $85
3-​ThiopheneboronicAcid T344640 1g $85
More product size

3-Thiopheneboronic acid Properties

Melting point 164-169 °C (lit.)
Boiling point 287.9±32.0 °C(Predicted)
Density 1.32±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility soluble in Methanol
form Powder
pka 8.25±0.10(Predicted)
color Almost white to grayish
BRN 113573
InChI InChI=1S/C4H5BO2S/c6-5(7)4-1-2-8-3-4/h1-3,6-7H
InChIKey QNMBSXGYAQZCTN-UHFFFAOYSA-N
SMILES C1SC=CC=1B(O)O
CAS DataBase Reference 6165-69-1(CAS DataBase Reference)
UNSPSC Code 12352103
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P264-P270-P301+P312-P302+P352-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xn,Xi
Risk Statements  22-36/37/38
Safety Statements  26-37/39-36
WGK Germany  3
Hazard Note  Irritant
HazardClass  IRRITANT, IRRITANT-HARMFUL, KEEP COLD
HS Code  29339900
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
0
2 0

3-Thiopheneboronic acid price More Price(37)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 436844 3-Thienylboronic acid ≥95.0% 6165-69-1 1g $40 2026-04-30 Buy
Sigma-Aldrich 436844 3-Thienylboronic acid ≥95.0% 6165-69-1 5g $81.1 2026-04-30 Buy
TCI Chemical T1975 3-Thiopheneboronic Acid (contains varying amounts of Anhydride) 6165-69-1 1g $30 2026-04-30 Buy
TCI Chemical T1975 3-Thiopheneboronic Acid (contains varying amounts of Anhydride) 6165-69-1 5g $85 2026-04-30 Buy
TRC T344640 3-​ThiopheneboronicAcid 6165-69-1 1g $85 2021-12-16 Buy
Product number Packaging Price Buy
436844 1g $40 Buy
436844 5g $81.1 Buy
T1975 1g $30 Buy
T1975 5g $85 Buy
T344640 1g $85 Buy

3-Thiopheneboronic acid Chemical Properties,Uses,Production

Chemical Properties

white to light yellow crystal powder

Uses

3-Thiopheneboronic Acid is used in the synthesis of porphyrins as inhibitiors of telomerase. It is also used to prepare 1,4-disubstituted imidazoles as potential antibacterial agents.

Uses

suzuki reaction

Synthesis

3-Bromothiophene

872-31-1

3-Thiopheneboronic acid

6165-69-1

General procedure for the synthesis of 3-thiophene boronic acid from 3-bromothiophene: Triphenylphosphine (0.131 g, 0.5 mmol, 20 mol%), p-iodoiodobenzene (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, a condenser, and a stir bar). The reaction system was degassed by alternating vacuum and argon filling three times. Palladium dichloride (0.023 g, 0.13 mmol, 5 mol%) was added under positive argon pressure. After stirring for 15 minutes at room temperature, diisopropylaminoborane (5 mL, 1 M THF solution, 5 mmol) was added and the reaction mixture was again degassed by alternating vacuum and argon filling three times. The reaction solution was heated to reflux and kept at reflux for 12 hours. Upon completion of the reaction, the reaction solution was cooled to 0 °C and 6 mL of methanol was slowly added (note: this is an exothermic reaction, which releases hydrogen). After stirring for 15 minutes, all solvent was removed by distillation under reduced pressure to give a black solid. The solid was dissolved in 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 3-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 3-thiopheneboronic acid in white solid form.

References

[1] Journal of Medicinal Chemistry, 2005, vol. 48, # 1, p. 224 - 239
[2] Organic Letters, 2011, vol. 13, # 17, p. 4479 - 4481
[3] Journal of Organic Chemistry, 2013, vol. 78, # 13, p. 6427 - 6439
[4] Patent: US6342610, 2002, B2. Location in patent: Page column 77
[5] Tetrahedron, 2011, vol. 67, # 3, p. 576 - 583

872-31-1
5419-55-6
6165-69-1
Synthesis of 3-Thiopheneboronic acid from 3-Bromothiophene and Triisopropyl borate
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View Lastest Price from 3-Thiopheneboronic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
3-Thiopheneboronic acid pictures 2025-04-04 3-Thiopheneboronic acid
6165-69-1
US $0.00-0.00 / kg 1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
3-Thiopheneboronic acid pictures 2019-07-06 3-Thiopheneboronic acid
6165-69-1
US $1.00 / KG 1G 98% 1000KG Career Henan Chemical Co
TIMTEC-BB SBB004244 (Thiophene-3-yl)boronic acid 3-Thiopheneboronic Acid (contains varyin… THIOPHENE-3-BORONIC ACID; 3-THIENYLBORONIC ACID 3-Boronothiophene 3-Thienylboronic acid >=95.0% RARECHEM AH PB 0232 AKOS BRN-0047 3-THIOPHENEBORONIC ACID 3-THIENYLBORONIC ACID THIOPHENYL-3-BORONIC ACID 3-ThiopheneBoricAcid Thiophene-3-boronicacid,98% 3-THIOPHENEBORONIC ACID ,THIOPHENE-3-BORONIC ACID THIOPHTNE-3-BORONIC ACID 3-Thiopheneboronic Acid (contains varying amounts of Anhydride) 3-Thiopheneboronic acid,97% 3-Thienylboronic acid,Thiophene-3-boronic acid 3-Thiopheneboronica thiophen-3-yl-3-boronic acid 3-Thiophenylboronic acid Thiophen-3-boronic acid Boronic acid, B-3-thienyl- 3-Thiopheneboronicaci THIOPHENE-3-BORONIC ACID THIOPHEN-3-YLBORONIC ACID 3-Thiopheneboronic acid?New 3-Thienylboronic acid > 97 % 3-thienoborate Thiophene-3-boronic acid - [T5200] 6165-69-1 6165-64-1 BORONIC ACID Boronic Acids and Derivatives Boronic Acids B (Classes of Boron Compounds) Heteroaryl Organometallic Reagents Boronic Acids and Derivatives Chemical Synthesis Heteroaryl Boronic Acids Organometallic Reagents Boric Acid| Boric Acid Ester| Potassium Trifluoroborate Boronate Ester Potassium Trifluoroborate B (Classes of Boron Compounds) CHIRAL CHEMICALS Boronic acid series Boronic Acid Organoborons Thiophene Azoles blocks BoronicAcids Organic acids Boronic acids Boron Compounds