Benzolsulfonamid

Benzenesulfonamide Struktur
98-10-2
CAS-Nr.
98-10-2
Bezeichnung:
Benzolsulfonamid
Englisch Name:
Benzenesulfonamide
Synonyma:
BSA;BENZENESULPHONAMIDE;CL160;mandb7973;benzsulfamide;Benzosuifqnamide;Benzenesulfomide;Benzosulfonamide;benzolsulfonamide;BENZENESULFONAMIDE
CBNumber:
CB4200738
Summenformel:
C6H7NO2S
Molgewicht:
157.19
MOL-Datei:
98-10-2.mol

Benzolsulfonamid Eigenschaften

Schmelzpunkt:
149-152 °C (lit.)
Siedepunkt:
315.5±25.0 °C(Predicted)
Dichte
1.274 (estimate)
Brechungsindex
1.5500 (estimate)
Flammpunkt:
250°C
storage temp. 
Store below +30°C.
Löslichkeit
methanol: soluble25mg/mL
pka
10.1(at 25℃)
Aggregatzustand
Powder, Crystals and/or Chunks
Farbe
White to off-white
Wasserlöslichkeit
4.3 g/L (16 ºC)
BRN 
1100566
InChIKey
KHBQMWCZKVMBLN-UHFFFAOYSA-N
CAS Datenbank
98-10-2(CAS DataBase Reference)
NIST chemische Informationen
Benzenesulfonamide(98-10-2)
EPA chemische Informationen
Benzenesulfonamide (98-10-2)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xn
R-Sätze: 22
S-Sätze: 36
WGK Germany  3
RTECS-Nr. DA9380000
TSCA  Yes
HS Code  29350090
Toxizität LD50 orally in Rabbit: 991 mg/kg
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
Sicherheit
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P301+P312 BEI VERSCHLUCKEN: Bei Unwohlsein GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P501 Inhalt/Behälter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

Benzolsulfonamid Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R22:Gesundheitsschädlich beim Verschlucken.

S-Sätze Betriebsanweisung:

S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.

Chemische Eigenschaften

white to off-white granular crystalline powder. insoluble in water, soluble in ethanol and ether. soluble in alkali.

Verwenden

Biospecific adsorption of carbonic anhydrase to self-assembled monolayers of alkanethiolates that present benzenesulfonamide groups on gold. Biospecific binding of carbonic anhydrase to mixed sams presenting benzenesulfonamide ligands led to a model system for studying lateral steric effects. Benzenesulfonamide modifications at c-7 of ciprofloxacin change its primary target instreptococcus pneumoniae from topoisomerase iv to gyrase. Polar substitutions in the benzenesulfonamide ring of celecoxib afford a potent 1,5-diarylpyrazole class of COX-2 inhibitors.

synthetische

Benzenesulfonamide is obtained by amination of benzenesulfonyl chloride.

Application

Benzenesulfonamides serve as intermediates in the production of polysulfonamides, which are used as tanning agents and plastics. N- Alkylamides of the benzenesulfonic and tolue-nesulfonic acids can be used as plasticizers. Aminobenzenesulfonamides and diaryldisulfonylamines with amino groups serve as intermediates in the production of azo dyes.

Sicherheitsprofil

Moderately toxic by ingestion andintraperitoneal routes. When heated to decomposition itemits very toxic fumes of SOx and NOx.

Properties and Applications

Benzenesulfonamides are readily crystallizing, colorless compounds with defined melting points and poor solubility in water. They are therefore suitable for the characterization of sulfonic acids (via the sulfonyl chlorides) and of primary and secondary amines and for the separation of amine mixtures (Hinsberg method). Benzenesulfonamides are weak acids and form salts with bases. They are thermally stable and very difficult to hydrolyze with alkali; however, they are more easily hydrolyzed with mineral acids. In concentrated sulfuric acid sodium nitrite splits them into sulfonic acids and nitrogen. The hydrogen atoms bound to the nitrogen can be substituted.

Benzolsulfonamid Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Benzolsulfonamid Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 398)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Shouguang Nuomeng Chemical Co Ltd.
536-5119508 18363669993;
export@nuomengchem.com China 44 58
Hebei Mojin Biotechnology Co., Ltd
+8613288715578
sales@hbmojin.com China 12456 58
airuikechemical co., ltd.
+undefined86-15315557071
sales02@airuikechemical.com China 994 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21691 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714
fandachem@gmail.com China 9348 55
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418679 +86-18949832763
info@tnjchem.com China 2989 55
career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29914 58
SHANDONG ZHI SHANG CHEMICAL CO.LTD
+86 18953170293
sales@sdzschem.com China 2931 58
Hubei Jusheng Technology Co.,Ltd.
18871490254
linda@hubeijusheng.com CHINA 28180 58
Hebei Guanlang Biotechnology Co., Ltd.
+86-19930503282
alice@crovellbio.com China 8823 58

98-10-2(Benzolsulfonamid)Verwandte Suche:


  • BenzenesulfonaMide, 98+% 500GR
  • Benzenesulfonamide Vetec(TM) reagent grade, 98%
  • Benzenesulfomide
  • BENZENESULFONYLAMIDE
  • BENZENESULFONAMIDE
  • Benzene sulfonamtde
  • Benzosuifqnamide
  • Benaenesulfonicamide
  • benzolsulfonamide
  • Benzosulfonamide
  • mandb7973
  • BENZENESULFONAMIDE, 98+%
  • Benzenesulfonamide (7CI,8CI,9CI)
  • Benzenesulfonamide(BSA)
  • benzenesulfonic amide
  • benzsulfamide
  • BENZENESULPHOAMIDE
  • phenyl sulfonamide
  • Benzene sulfonamide, BSA, Benzenesulfonamide
  • Benzenesulfonamide >
  • BENZENESULFONAMIDE FOR SYNTHESIS
  • Benzenesulfonamide ISO 9001:2015 REACH
  • Benzenesulfonamide (Benzenesulphonamide, Benzosulfonamide)
  • 98-10-2 Benzenesulfonamide
  • 4'-Anhydrovinblastine
  • CL160
  • BENZENESULPHONAMIDE
  • BSA
  • Benzen Sulphanamide
  • Benzene sulphonamide (84%,99.5%)
  • Benzenesulfonamide, ≥ 98.0%
  • 98-10-2
  • 1998-10-2
  • 36-07-0
  • 1998-10-02
  • C6H7N1O2S1
  • C6H6NO2S
  • C6H5SO2NH2
  • C6H7O2NS
  • Organic Building Blocks
  • Sulfur Compounds
  • Sulfonamides/Sulfinamides
  • Building Blocks
  • Urinary System Agents
  • Organic Building Blocks
  • Sulfonamides/Sulfinamides
  • Sulfur Compounds
  • Pharmaceutical Intermediates
  • SULFONAMIDE
  • Benzene derivatives
  • Organics
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