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3-Bromothiophene-2-carbaldehyde

CAS No.
930-96-1
Chemical Name:
3-Bromothiophene-2-carbaldehyde
Synonyms
3-BROMOTHIOPHENE-2-CARBOXALDEHYDE;THCHO-Br;BUTTPARK 43\57-52;3-Bromothiophene-2;3-Bromo-2-Formylthophene;3-BROMO-2-FORMYLTHIOPHENE;3-BROMO-2-THIOPHENECARBALDEHYDE;3-BROMOTHIOPHENE-2-CARBALDEHYDE;3-bromothiophene-2-formaldehyde;3-Bromo-2-thiophenecarboxaldehyde
CBNumber:
CB4290245
Molecular Formula:
C5H3BrOS
Molecular Weight:
191.05
MDL Number:
MFCD00126680
MOL File:
930-96-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 01:16:37

3-Bromothiophene-2-carbaldehyde Properties

Melting point 25 °C
Boiling point 77-79°C 0,2mm
Density 1.755 g/mL at 25 °C
refractive index 1.6377
Flash point 110-113°C/10mm
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
form clear liquid
color Light yellow to Amber to Dark green
Water Solubility Not miscible in water.
Sensitive Air Sensitive
BRN 109757
InChI InChI=1S/C5H3BrOS/c6-4-1-2-8-5(4)3-7/h1-3H
InChIKey BCZHCWCOQDRYGS-UHFFFAOYSA-N
SMILES C1(C=O)SC=CC=1Br
CAS DataBase Reference 930-96-1(CAS DataBase Reference)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P280a-P305+P351+P338-P321-P332+P313-P337+P313-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Hazard Codes  Xi,Xn
Risk Statements  36/38-36/37/38-20/21/22
Safety Statements  26-36/37/39-22-37/39
WGK Germany  3
HazardClass  IRRITANT
HS Code  29349990
Storage Class 11 - Combustible Solids
NFPA 704
1
2 0

3-Bromothiophene-2-carbaldehyde price More Price(109)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 716553 3-Bromothiophene-2-carboxaldehyde 96% 930-96-1 1g $41.9 2026-04-30 Buy
TCI Chemical B2934 3-Bromothiophene-2-carboxaldehyde >95.0%(GC) 930-96-1 1g $29 2026-04-30 Buy
TCI Chemical B2934 3-Bromothiophene-2-carboxaldehyde >95.0%(GC) 930-96-1 5g $98 2026-04-30 Buy
Usbiological 261701 3-Bromothiophene-2-carbaldehyde Asreported 930-96-1 1g $315 2026-06-03 Buy
Usbiological 261701 3-Bromothiophene-2-carbaldehyde Asreported 930-96-1 2g $430 2026-06-03 Buy
Product number Packaging Price Buy
716553 1g $41.9 Buy
B2934 1g $29 Buy
B2934 5g $98 Buy
261701 1g $315 Buy
261701 2g $430 Buy

3-Bromothiophene-2-carbaldehyde Chemical Properties,Uses,Production

Chemical Properties

Colorless to yellow liquid

Uses

3-Bromothiophene-2-carboxaldehyde is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

Synthesis Reference(s)

Journal of Medicinal Chemistry, 34, p. 1805, 1991 DOI: 10.1021/jm00110a008

Synthesis

3-Bromothiophene

872-31-1

N,N-Dimethylformamide

68-12-2

3-Bromothiophene-2-carbaldehyde

930-96-1

Diisopropylamine (51.6 kg, 509.9 mol, 1.0 eq.) and anhydrous tetrahydrofuran (THF) (385.0 kg) were added to a 1000 L autoclave under nitrogen protection. After cooling the system to 0-5 °C, n-butyllithium (BuLi) (131.4 kg, 463.8 mol, 1.0 eq.) was slowly added. After addition, stirring was continued at 0-5 °C for 30 min. Subsequently, a solution of 3-bromothiophene (75.0 kg, 460.0 mol, 1.0 eq.) in THF (20.0 kg) was added dropwise. After dropwise addition, stirring was continued at 0-5 °C for 30 min. Next, a solution of N,N-dimethylformamide (DMF) (35.3 kg, 473.3 mol, 1.0 eq.) in THF (10.0 kg) was slowly added dropwise. After completion of dropwise addition, stirring was maintained at 0-5 °C for 3 hours. Upon completion of the reaction, a 14% aqueous ammonium chloride (NH4Cl) solution (700.0 g) was slowly added dropwise at 0-5 °C. After addition, the reaction was stirred at 0-5 °C for 15 min and allowed to stand for 15 min. The organic phase was separated and stored temporarily in a clean PTFE drum. The aqueous phase was re-pumped into the reactor, methyl tertiary butyl ether (MTBE) (150.0 kg) was added, stirred for 15 min, and allowed to stand for 15 min before separating the phase and collecting the upper organic phase. All organic phases were combined and dried with anhydrous sodium sulfate (85.0 kg) for several hours until the moisture content was <1%. Filtration, the filter cake was washed with methyl tert-butyl ether (20 mL x 2), the filtrates were combined and concentrated under reduced pressure to remove the solvent to give 3-bromothiophene-2-carbaldehyde (93.8 kg, 100% yield).

References

[1] Patent: CN103172646, 2016, B. Location in patent: Paragraph 0101-0104
[2] European Journal of Organic Chemistry, 2016, vol. 2016, # 31, p. 5263 - 5273
[3] Macromolecules, 2013, vol. 46, # 6, p. 2078 - 2091
[4] Tetrahedron Letters, 2012, vol. 53, # 2, p. 166 - 169
[5] Journal of the American Chemical Society, 2014, vol. 136, # 19, p. 7132 - 7139

Global( 273)Suppliers
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View Lastest Price from 3-Bromothiophene-2-carbaldehyde manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
3-Bromo-2-thiophenecarbaldehyde pictures 2026-09-02 3-Bromo-2-thiophenecarbaldehyde
930-96-1
$1.00-200.00 1KG 99%, 99.5% Sublimated Henan Fengda Chemical Co., Ltd
3-Bromothiophene-2-carbaldehyde  pictures 2026-08-20 3-Bromothiophene-2-carbaldehyde
930-96-1
$1.10 1g 99.00% 100 Tons Dideu Industries Group Limited
3-Bromothiophene-2-carbaldehyde pictures 2025-04-04 3-Bromothiophene-2-carbaldehyde
930-96-1
1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
BUTTPARK 43\57-52 3-BROMOTHIOPHENE-2-CARBOXALDEHYDE 3-BROMOTHIOPHENE-2-CARBALDEHYDE 3-BROMO-2-FORMYLTHIOPHENE 3-BROMO-2-THIOPHENECARBALDEHYDE 3-Bromothiophene-2-carboxaldehyde, 95%+ 3-Bromo-2-Formylthophene 3-Bromothiophene-2-carboxaldehyde, GC 97% 3-BROMOTHIOPHENE-2-CARBOXALDEHYDE 98% 3-Bromo-2-thiophenecarboxaldehyde 3-bromothiophene-2-formaldehyde 3-Bromo-2-formylthiophene, 3-Bromo-2-thenaldehyde THCHO-Br 3-Bromothiophene-2-carboxaldehyde > 3-Bromothiophene-2-carbaldehyde ISO 9001:2015 REACH 3-bromothiophene-2- 4-carbaldehyde 3-Bromothiophene-2 930-96-1 Aldehydes Building Blocks C1 to C6 C4 to C6 Carbonyl Compounds Chemical Synthesis Heterocyclic Building Blocks Organic Building Blocks Thiophenes Azoles blocks Bromides Thiophene&Benzothiophene Functional Materials Reagents for Conducting Polymer Research Thiophene Derivatives (for Conduting Polymer Research) Thiophen