N-Acetylsulfanilyl chloride - CAS 121-60-8
Catalog: |
BB005222 |
Product Name: |
N-Acetylsulfanilyl chloride |
CAS: |
121-60-8 |
Synonyms: |
4-acetamidobenzenesulfonyl chloride |
IUPAC Name: | 4-acetamidobenzenesulfonyl chloride |
Description: | A sulfanilamide derivative of Chitosan with antifungal properties. |
Molecular Weight: | 233.67 |
Molecular Formula: | C8H8ClNO3S |
Canonical SMILES: | CC(=O)NC1=CC=C(C=C1)S(=O)(=O)Cl |
InChI: | InChI=1S/C8H8ClNO3S/c1-6(11)10-7-2-4-8(5-3-7)14(9,12)13/h2-5H,1H3,(H,10,11) |
InChI Key: | GRDXCFKBQWDAJH-UHFFFAOYSA-N |
Boiling Point: | 426.8 °C at 760 mmHg |
Melting Point: | 145-148 °C |
Purity: | 95 % |
Density: | 1.468 g/cm3 |
Appearance: | Off-white to slightly grey granular cryst powder |
Storage: | Keep container closed when not in use. Store in a tightly closed container. Store in a dry area. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. |
MDL: | MFCD00007442 |
LogP: | 2.72630 |
GHS Hazard Statement: | H314 (51.61%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation] |
Precautionary Statement: | P260, P261, P264, P271, P273, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P363, P391, P403+P233, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113336680-A | Environment-friendly technological synthesis method of sulfanilamide | 20210604 |
CN-113292476-A | Sulfaindole derivative and preparation method and application thereof | 20210518 |
CN-113321578-A | Green process for industrial sulfanilamide co-production hydroxylamine product and organic acid downstream product recycling economy industrial chain | 20210518 |
CN-113200974-A | Pharmaceutical composition, furaltadone hydrochloride and preparation method and application method thereof | 20210430 |
CN-112851559-A | FtsZ and QseC double-target antibacterial molecule and preparation method and application thereof | 20210123 |
PMID | Publication Date | Title | Journal |
23030435 | 20130101 | Synthesis of hapten and production of a monoclonal antibody against a derivative of L-hydroxyproline, a special amino acid in hydrolyzed animal protein | Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes |
22590212 | 20120501 | 2-{4-[Acet-yl(eth-yl)amino]-benzene-sulfonamido}-benzoic acid | Acta crystallographica. Section E, Structure reports online |
22346929 | 20120201 | N-[4-(Propyl-sulfamo-yl)phen-yl]acetamide | Acta crystallographica. Section E, Structure reports online |
22059023 | 20110901 | N-[4-(Ethyl-sulfamo-yl)phen-yl]acetamide | Acta crystallographica. Section E, Structure reports online |
21836982 | 20110701 | 2-(4-Acetamido-benzene-sulfonamido)-benzoic acid | Acta crystallographica. Section E, Structure reports online |
Complexity: | 301 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 232.991342 |
Formal Charge: | 0 |
Heavy Atom Count: | 14 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 232.991342 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 71.6 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.4 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Sulfur Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS