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5-Bromothiophenesulfonyl chloride

CAS No.
55854-46-1
Chemical Name:
5-Bromothiophenesulfonyl chloride
Synonyms
5-BROMOTHIOPHENE-2-SULFONYL CHLORIDE;SBB003086;AKOS B019399;636223_ALDRICH;AKOS BBS-00004606;BUTTPARK 21\07-09;5-bromothiophene-2;TIMTEC-BB SBB003086;ART-CHEM-BB B019399;5-Bromothiophenesulf
CBNumber:
CB3266418
Molecular Formula:
C4H2BrClO2S2
Molecular Weight:
261.54
MDL Number:
MFCD00084909
MOL File:
55854-46-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-08-27 08:49:46

5-Bromothiophenesulfonyl chloride Properties

Melting point 40-44 °C (lit.)
Boiling point 100-102 °C/0.5 mmHg (lit.)
Density 1.985±0.06 g/cm3(Predicted)
Flash point >230 °F
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
form crystalline powder
color Off-white/ faint lemon
Sensitive Moisture Sensitive
InChI 1S/C4H2BrClO2S2/c5-3-1-2-4(9-3)10(6,7)8/h1-2H
InChIKey WGYBIEOLAFYDEC-UHFFFAOYSA-N
SMILES ClS(=O)(=O)c1ccc(Br)s1
CAS DataBase Reference 55854-46-1(CAS DataBase Reference)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
Signal word  Danger
Hazard statements  H314-H317
Precautionary statements  P260-P272-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  C,Xi,Xn
Risk Statements  34-43-36/37/38-20/21/22
Safety Statements  26-36/37/39-45-28A-25-36
RIDADR  UN 3261 8/PG 2
WGK Germany  3
Hazard Note  Harmful/Corrosive
HazardClass  8
PackingGroup  II
HS Code  29349990
Storage Class 8A - Combustible corrosive hazardous materials
Hazard Classifications Skin Corr. 1B
Skin Sens. 1
Limited Quantities 5.0 kg (11 lbs) (solid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (1Kg or 1L)
NFPA 704
0
3 0

5-Bromothiophenesulfonyl chloride price More Price(71)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 636223 5-Bromothiophene-2-sulfonyl chloride 97% 55854-46-1 5g $134 2026-04-30 Buy
Sigma-Aldrich 636223 5-Bromothiophene-2-sulfonyl chloride 97% 55854-46-1 25g $676 2023-06-20 Buy
TCI Chemical B2878 5-Bromo-2-thiophenesulfonyl Chloride >98.0%(GC)(T) 55854-46-1 1g $39 2021-12-16 Buy
TCI Chemical B2878 5-Bromo-2-thiophenesulfonyl Chloride >98.0%(GC)(T) 55854-46-1 5g $77 2021-12-16 Buy
AstaTech 56142 5-BROMO-THIOPHENE-2-SULFONYL CHLORIDE 95% 55854-46-1 25G $45 2026-04-30 Buy
Product number Packaging Price Buy
636223 5g $134 Buy
636223 25g $676 Buy
B2878 1g $39 Buy
B2878 5g $77 Buy
56142 25G $45 Buy

5-Bromothiophenesulfonyl chloride Chemical Properties,Uses,Production

Chemical Properties

light yellow crystalline low melting solid

Uses

5-Bromothiophene-2-sulfonyl chloride serves as a starting material for the synthesis of sulfonamide compounds[1]. The reagent reacts with 4-chloroanisole to yield the corresponding sulfone product, and couples with 2-aminobenzoic acid in acetone at room temperature using DMAP[1][3]. It functionalizes m-THPP via sulfonate linkers in dry THF with K2CO3, where base selection and temperature control the distribution of mono- and tetrasubstituted derivatives[2]. The compound acts as a sulfonylating agent in dichloromethane with triethylamine, and reacts with glycine tert-butyl ester hydrochloride in a dioxane/water mixture containing Et3N[4][5].

References

[1] Liu, J.-P., Zheng, Y.-B. (2007). 5-Bromothiophene-2-sulfonic acid. Acta Crystallographica Section E Structure Reports Online, 63(9), o3697–o3697. https://doi.org/10.1107/s1600536807037208
[2] Shaker, Y. M., Omar, M. A., Grover, N., Senge, M. O. (2022). Facile synthesis of porphyrin-conjugates as amphiphilic modified photosensitizer structures of m-THPP bearing carbamate, carboxylate and sulfonate linkers. Journal of Porphyrins and Phthalocyanines, 26(10), 638–647. https://doi.org/10.1142/s1088424622500468
[3] Garzya, V., Forbes, I. T., Lauru, S., Maragni, P. (2004). Indium(III)-catalysed aryl sulfonylation reactions. Tetrahedron Letters, 45(7), 1499–1501. https://doi.org/10.1016/j.tetlet.2003.12.028
[4] Dai, Z., Yang, X., Li, Y., Bai, C., Wang, K., Huang, J., Wen, X., Wu, X., Ding, J., Peng, T., He, Y. (2026). Discovery and synthesis of phenylthiophene sulfonamide derivatives with promising anti-inflammatory activity. RSC Advances, 16(37), 40019–40034. https://doi.org/10.1039/d6ra03406c
[5] Nuti, E., Casalini, F., Santamaria, S., Gabelloni, P., Bendinelli, S., Pozzo, E. D., Costa, B., Marinelli, L., Pietra, V. L., Novellino, E., Bernardo, M. M., Fridman, R., Settimo, F. D., Martini, C., Rossello, A. (2011). Synthesis and biological evaluation in U87MG glioma cells of (ethynylthiophene)sulfonamido-based hydroxamates as matrix metalloproteinase inhibitors. European Journal of Medicinal Chemistry, 46(7), 2617–2629. https://doi.org/10.1016/j.ejmech.2011.03.033

1003-09-4
55854-46-1
Synthesis of 5-Bromothiophenesulfonyl chloride from 2-Bromothiophene

5-Bromothiophenesulfonyl chloride Preparation Products And Raw materials

Global( 282)Suppliers
Supplier Tel Email Country ProdList Advantage
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
INTATRADE GmbH +49 3493/605464 sales@intatrade.de Germany 3563 66
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30103 84
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Wuhan Chemwish Technology Co., Ltd 86-027-67849912 sales@chemwish.com China 35884 56
Capot Chemical Co., Ltd +86 (0) 571 85 58 67 18 China 18187 66
JinYan Chemicals(ShangHai) Co.,Ltd. 13817811078 sales@jingyan-chemical.com China 9963 60
Shanghai Sinch Parmaceuticals Tech. Co. Ltd. +86-21-54098501 sales@sinch.com.cn China 11592 64

View Lastest Price from 5-Bromothiophenesulfonyl chloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
5-Bromothiophenesulfonyl chloride  pictures 2026-08-20 5-Bromothiophenesulfonyl chloride
55854-46-1
$1.10 1g 99.00% 100 Tons Dideu Industries Group Limited
5-Bromothiophenesulfonyl chloride pictures 2025-04-04 5-Bromothiophenesulfonyl chloride
55854-46-1
1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
5-Bromo-thiophene-2-sulfonyl chloride pictures 2024-02-19 5-Bromo-thiophene-2-sulfonyl chloride
55854-46-1
$890.00 1g 96 500 Kg R&D Scientific Inc.

5-Bromothiophenesulfonyl chloride Spectrum

5-Bromothiophene-2-Sulfonyl 5-Bromothiophenesulfonyl 5-BROMOTHIOPHENESULFONYLCHLORIDE,96% 5-BROMOTHIOPHENE-2-SUPHONYLCHLORIDE 5-Bromo-2-thiophenensulfonyl Chloride 5-Bromothiophenesulf 5-bromothiophene-2-sulfonyl chloride(SALTDATA: FREE) 5-Bromothiophene-2-sulphonyl chloride 98% 5-Bromo-2-(chlorosulphonyl)thiophene 5-Bromothiophen-2-sulfonyl chloride 5-BroMothiophenesulfonyl chloride, 96% 1GR 5-Bromothiophene-2-sulfonylchloride,98% 5-Bromothiophene-2-sulfonyl chloride 97% 636223_ALDRICH SBB003086 TIMTEC-BB SBB003086 5-BROMOTHIOPHENE-2-SULPHONYL CHLORIDE 5-BROMOTHIOPHENESULFONYL CHLORIDE 5-BROMOTHIOPHENESULPHONYL CHLORIDE 5-BROMO-2-THIOPHENESULFONYL CHLORIDE AKOS B019399 AKOS BBS-00004606 ART-CHEM-BB B019399 BUTTPARK 21\07-09 2-BROMOTHIOPHENE-5-SULFONYL CHLORIDE 5-bromothiophene-2 5-Bromo-2-thiophenesulfonyl Chloride > 5-Bromothiophene-2-suL 2-Thiophenesulfonyl chloride, 5-bromo- 5-Bromothiophenesulfonyl chloride ISO 9001:2015 REACH 5-BROMOTHIOPHENE-2-SULFONYL CHLORIDE 55854-46-1 55854-43-1 C4H2BrClO2S2 C4H2BrClS2O2 SULFONYL CHLORIDE Halogenated Heterocycles Heterocyclic Building Blocks Thiophenes Building Blocks Sulphonyl Chlorides Thiophenes & Benzothiophenes Heterocycles Halogenated Heterocycles Heterocyclic Building Blocks Thiophenes ThiophenesBuilding Blocks Fluorobenzene Sulphonyl Chlorides Thiophenes & Benzothiophenes Thiophene&Benzothiophene Thiophene intermediates