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3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE

CAS No.
23094-96-4
Chemical Name:
3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE
Synonyms
3-broMo-4-Methoxybenzene-1-sulfonyl chloride;3-Bromo-4-methoxybenzenesulfonylchloride,97%;Benzenesulfonyl chloride, 3-bromo-4-methoxy-;3-Bromo-4-methoxybenzenesulfonyl chloride 97%;3-bromo-4-methoxybenzenesulfonyl chloride(SALTDATA: FREE)
CBNumber:
CB01492572
Molecular Formula:
C7H6BrClO3S
Molecular Weight:
285.54
MDL Number:
MFCD03989643
MOL File:
23094-96-4.mol
MSDS File:
SDS
Last updated:2026-06-04 16:00:12
Product description Number Pack Size Price
3-Bromo-4-methoxybenzenesulfonyl chloride 97% 749346 1g $34
3-Bromo-4-methoxy-benzenesulfonyl chloride >96% OR480728 250mg $21
3-Bromo-4-methoxy-benzenesulfonyl chloride >96% OR480728 1g $24
3-Bromo-4-methoxy-benzenesulfonyl chloride >96% OR480728 5g $89
3-Bromo-4-methoxy-benzenesulfonyl chloride >96% OR480728 25g $437

3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE Properties

Melting point 83-88°C
Boiling point 366.0±27.0 °C(Predicted)
Density 1.717±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form solid
Appearance Off-white to pink Solid
Sensitive Moisture Sensitive
InChI 1S/C7H6BrClO3S/c1-12-7-3-2-5(4-6(7)8)13(9,10)11/h2-4H,1H3
InChIKey LTVLATJRJIBHDR-UHFFFAOYSA-N
SMILES COc1ccc(cc1Br)S(Cl)(=O)=O
CAS DataBase Reference 23094-96-4
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  H302-H314
Precautionary statements  P260-P270-P280-P301+P312-P303+P361+P353-P305+P351+P338
Hazard Codes  C
Risk Statements  22-34
Safety Statements  26-36/37/39-45
RIDADR  UN 3261 8 / PGII
WGK Germany  3
HazardClass  8
HazardClass  IRRITANT
HS Code  2930909899
Storage Class 8A - Combustible corrosive hazardous materials
Hazard Classifications Acute Tox. 4 Oral
Skin Corr. 1B
Limited Quantities 1 Kg (2.2 lbs) (solid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
NFPA 704
1
3 0

3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE price More Price(49)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 749346 3-Bromo-4-methoxybenzenesulfonyl chloride 97% 23094-96-4 1g $34 2023-06-20 Buy
Apolloscientific OR480728 3-Bromo-4-methoxy-benzenesulfonyl chloride >96% 23094-96-4 250mg $21 2026-06-04 Buy
Apolloscientific OR480728 3-Bromo-4-methoxy-benzenesulfonyl chloride >96% 23094-96-4 1g $24 2026-06-04 Buy
Apolloscientific OR480728 3-Bromo-4-methoxy-benzenesulfonyl chloride >96% 23094-96-4 5g $89 2026-06-04 Buy
Apolloscientific OR480728 3-Bromo-4-methoxy-benzenesulfonyl chloride >96% 23094-96-4 25g $437 2026-06-04 Buy
Product number Packaging Price Buy
749346 1g $34 Buy
OR480728 250mg $21 Buy
OR480728 1g $24 Buy
OR480728 5g $89 Buy
OR480728 25g $437 Buy

3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE Chemical Properties,Uses,Production

Synthesis

2-Bromoanisole

578-57-4

3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE

23094-96-4

General procedure for the synthesis of 3-bromo-4-methoxybenzene-1-sulfonyl chloride from 2-bromoanisole: 2-bromo-1-methoxybenzene (1.87 g, 10.0 mmol) was dissolved in chloroform (5 mL), and the solution was cooled in an iced salt bath to -5 °C to 0 °C. Chlorosulfonic acid (2.0 mL, 30.0 mmol) was slowly added dropwise over 30 minutes, and after completion of the dropwise addition, the reaction mixture was gradually warmed to room temperature over 1 hour. Subsequently, the reaction mixture was poured onto crushed ice and transferred to a dispensing funnel. The aqueous layer was separated and extracted twice with chloroform. The organic layers were combined, dried and concentrated to give 3-bromo-4-methoxybenzenesulfonyl chloride (2.80 g, 98%). 3-Bromo-4-methoxybenzenesulfonyl chloride (2.80 g, 9.8 mmol) was dissolved in dichloromethane (30 mL), triethylamine (1.76 mL, 12.6 mmol) was added to the solution, followed by slow dropwise addition of tert-butylamine (1.33 mL, 12.6 mmol). The reaction mixture was allowed to stand for 2 hours and then poured into a mixture of 5% citric acid solution and dichloromethane. The organic layer was separated and the aqueous layer was extracted twice with dichloromethane. The organic layers were combined, dried and concentrated. The crude product was recrystallized by ethyl acetate/hexane mixed solvent to give 3-bromo-N-tert-butyl-4-methoxybenzenesulfonamide (2.43 g, 77%).

References

[1] Patent: WO2004/50637, 2004, A2. Location in patent: Page 68-69
[2] Patent: WO2004/62661, 2004, A1. Location in patent: Page/Page column 24-25; 37-38
[3] Patent: US2015/25068, 2015, A1. Location in patent: Paragraph 0794
[4] Journal of the Chemical Society [Section] C: Organic, 1969, p. 1341 - 1345
[5] Bioorganic and Medicinal Chemistry Letters, 1997, vol. 7, # 4, p. 485 - 488

578-57-4
23094-96-4
Synthesis of 3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE from 2-Bromoanisole

3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE Preparation Products And Raw materials

3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE Suppliers

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3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE Spectrum

3-bromo-4-methoxybenzenesulfonyl chloride(SALTDATA: FREE) 3-broMo-4-Methoxybenzene-1-sulfonyl chloride 3-Bromo-4-methoxybenzenesulfonyl chloride 97% Benzenesulfonyl chloride, 3-bromo-4-methoxy- 3-Bromo-4-methoxybenzenesulfonylchloride,97% 23094-96-4