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2,5-DIFLUOROBENZENESULFONYL CHLORIDE

Product Name
2,5-DIFLUOROBENZENESULFONYL CHLORIDE
CAS No.
26120-86-5
Chemical Name
2,5-DIFLUOROBENZENESULFONYL CHLORIDE
Synonyms
AKOS B019395;BUTTPARK 21\07-13;ART-CHEM-BB B019395;2,5-DIAMIONPYRIMIDINE;2,5-Difluorobenzenesulphonylchlori;2,5-DIFLUOROBENZENESULFONYL CHLORIDE;2,3-Difluorobenzenesulfonyl chloride;2,5-DIFLUOROBENZENESULPHONYL CHLORIDE;2,5-Difluorobenzenesulphonylchloride98%;2,5-difluorobenzene-1-sulfonyl chloride
CBNumber
CB7456219
Molecular Formula
C6H3ClF2O2S
Formula Weight
212.6
MOL File
26120-86-5.mol
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2,5-DIFLUOROBENZENESULFONYL CHLORIDE Property

Boiling point:
221 °C (lit.)
Density 
1.58 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.516(lit.)
Flash point:
>230 °F
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
liquid
color 
Clear, yellow/green
Sensitive 
Moisture Sensitive
BRN 
2723886
CAS DataBase Reference
26120-86-5(CAS DataBase Reference)
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Safety

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-36/37/39-45
RIDADR 
UN 3265 8/PG 2
WGK Germany 
3
Hazard Note 
Corrosive
HazardClass 
8
PackingGroup 
II
HS Code 
29049090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H314Causes severe skin burns and eye damage

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

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

P363Wash contaminated clothing before reuse.

P405Store locked up.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
555428
Product name
2,5-Difluorobenzenesulfonyl chloride
Purity
97%
Packaging
5g
Price
$50.8
Updated
2023/06/20
Sigma-Aldrich
Product number
555428
Product name
2,5-Difluorobenzenesulfonyl chloride
Purity
97%
Packaging
1g
Price
$24
Updated
2023/01/07
TRC
Product number
D451393
Product name
2,5-Difluorobenzenesulfonyl chloride
Packaging
2.5g
Price
$65
Updated
2021/12/16
TRC
Product number
D451393
Product name
2,5-Difluorobenzenesulfonyl chloride
Packaging
5g
Price
$75
Updated
2021/12/16
TRC
Product number
D451393
Product name
2,5-Difluorobenzenesulfonyl chloride
Packaging
500mg
Price
$45
Updated
2021/12/16
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2,5-DIFLUOROBENZENESULFONYL CHLORIDE Chemical Properties,Usage,Production

Chemical Properties

Clear colorless to yellow liquid

General Description

2,5-Difluorobenzenesulfonyl chloride participates in the synthesis of aryl sulfonamide-based mineralocorticoid receptor (MR) antagonists.

Synthesis

367-30-6

26120-86-5

The general procedure for the synthesis of 2,5-difluorobenzenesulfonyl chloride from 2,5-difluoroaniline was as follows: 12.9 g (99.9 mmol) of 2,5-difluoroaniline was rapidly added to a mixture prepared from 33 mL of concentrated hydrochloric acid and 10 mL of acetic acid in ethanol cooled to just below -10°C. The solution of 2,5-difluorobenzenesulfonyl chloride in ethanol was then added dropwise. Subsequently, a solution of 7.4 g (107 mmol) of sodium nitrite dissolved in 15 mL of water was added dropwise. After the dropwise addition, stirring was continued for 45 minutes at a temperature range of -10 to -25°C. Maintaining the temperature of the reaction solution at about -25 °C, a mixture consisting of 100 mL of acetic acid saturated with sulfur dioxide and 2.5 g (25.3 mmol) cuprous chloride was added in batches, a process that required cooling to 10 °C in an ice bath. A large amount of nitrogen generation was observed during the reaction. The reaction mixture was brought back to room temperature and kept for 2 h. Subsequently, it was poured into 450 mL of ice-water mixture and extracted with ether. The ether extracts were combined, washed with saturated aqueous sodium bicarbonate, dried over sodium sulfate and concentrated. The resulting oily residue was distilled under reduced pressure to give 14.3 g (87% yield) of a liquid product consisting mainly of 2,5-difluorobenzenesulfonyl chloride with a boiling point of 65-70 °C (0.5 mmHg), which could be used in subsequent steps without further purification.

References

[1] Patent: US6509499, 2003, B1
[2] Journal of Chemical Information and Modeling, 2015, vol. 54, # 12, p. 3404 - 3416

2,5-DIFLUOROBENZENESULFONYL CHLORIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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2,5-DIFLUOROBENZENESULFONYL CHLORIDE Suppliers

J & K SCIENTIFIC LTD.
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18210857532; 18210857532
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86-10-82849933
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jkinfo@jkchemical.com
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China
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Alfa Aesar
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400-6106006
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021-67582001/03/05
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saleschina@alfa-asia.com
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China
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Energy Chemical
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Wuhan Chemwish Technology Co., Ltd
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86-027-67849912
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86-027-87531808
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sales@chemwish.com
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China
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Capot Chemical Co., Ltd
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+86 (0) 571 85 58 67 18
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0086-571-85864795
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Beijing Ouhe Technology Co., Ltd
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010-010-82967028 13522913783
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+86-10-82967029
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2355560935@qq.com
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JinYan Chemicals(ShangHai) Co.,Ltd.
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Shanghai Sinch Parmaceuticals Tech. Co. Ltd.
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+86-21-54096319
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sales@sinch.com.cn
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China
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Shanghai Hanhong Scientific Co.,Ltd.
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021-54306202 13764082696
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info@hanhongsci.com
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China
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China DongFan Chemical Co.,LTD
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86-0571-85151182
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86-0571-85151182
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China
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View Lastest Price from 2,5-DIFLUOROBENZENESULFONYL CHLORIDE manufacturers

Career Henan Chemical Co
Product
2,5-DIFLUOROBENZENESULFONYL CHLORIDE 26120-86-5
Price
US $1.00/KG
Min. Order
1KG
Purity
95-99%
Supply Ability
100kg/week
Release date
2019-08-05

26120-86-5, 2,5-DIFLUOROBENZENESULFONYL CHLORIDERelated Search:


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  • 2,5-DIFLUOROBENZENESULPHONYL CHLORIDE
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  • AKOS B019395
  • ART-CHEM-BB B019395
  • BUTTPARK 21\07-13
  • 2,5-Difluorobenzenesulphonyl chloride 98%
  • 2,5-Difluorobenzenesulphonylchloride98%
  • 2,3-Difluorobenzenesulfonyl chloride
  • 2,5-DIAMIONPYRIMIDINE
  • 2,5-Difluorobenzenesulfonyl chloride 97%
  • 2,5-Difluorobenzenesulphonylchlori
  • Benzenesulfonyl chloride, 2,5-difluoro-
  • 26120-86-5
  • C6H3F2ClO2S
  • SULFONYL CHLORIDE
  • Building Blocks
  • Sulfonyl Halides
  • Sulfur Compounds
  • Organic Building Blocks
  • Fluorine series
  • Aromatic Halides (substituted)
  • Benzenesulfonyl chloride
  • Organic Building Blocks
  • Sulfonyl Halides
  • Sulfur Compounds