5339-67-3

Basic information

• Product Name: N-ETHYLBENZSULFAMIDE
• Synonyms: n-ethyl-benzenesulfonamid;n-ethylbenzenesulfonamide;N-Ethyl-benzenesulfonamide;N-ETHYLBENZSULFAMIDE;Ai3-01082;Brn 2096148;Nsc 3547
• CAS NO: 5339-67-3
• Molecular Formula: C₈H₁₁NO₂S
• Molecular Weight: 185.24
• Mol File: 5339-67-3.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 297.9°Cat760mmHg
• Flash Point: 134°C
• Appearance: /
• Density: 1.183g/cm³
• Vapor Pressure: 0.00131mmHg at 25°C
• Refractive Index: 1.531
• CAS DataBase Reference: N-ETHYLBENZSULFAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-ETHYLBENZSULFAMIDE(5339-67-3)
• EPA Substance Registry System: N-ETHYLBENZSULFAMIDE(5339-67-3)

Safety Data

• Hazardous Substances Data: 5339-67-3(Hazardous Substances Data)

Usage

Uses

Agricultural chemical.

Hazard

Moderately toxic by ingestion.

InChI:InChI=1/C8H11NO2S/c1-2-9-12(10,11)8-6-4-3-5-7-8/h3-7,9H,2H2,1H3

Upstream product

• 67-56-1 methanol 
• 74805-37-1 N-Benzyl-N-ethyl-benzenesulfonamide 
• 557-66-4 ethanamine hydrochloride 
• 98-09-9 benzenesulfonyl chloride 
• 75-04-7 ethylamine 
• 155164-57-1 2-benzenesulfonyl-4,5-dichloropyridazin-3-one 
• 5661-14-3 N-(phenylsulfonyl)acetamide 
• 98-10-2 benzenesulfonamide 
• 627-48-5 ethyl cyanate 
• 970-88-7 2,4-dinitrophenyl benzenesulfonate 

Downstream Products

• 60989-15-3 C₁₆H₂₀N₂O₄S₂ 
• 1312206-44-2 N-ethyl-2-(pyridin-2-yl)benzenesulfonamide 
• 74805-36-0 N-ethyl-N-methyl benzenesulfonamide 
• 98-10-2 benzenesulfonamide 
• 312-63-0 N-(4-fluorophenyl)benzenesulfonamide 
• 1678-25-7 N-phenylbenzenesulfonamide 
• 96199-50-7 N-Aethyl-N-phenylsulfonyl-formamid-diaethylacetal 
• 66896-75-1 N-(2-Chloro-benzoyl)-N-ethyl-benzenesulfonamide 

Relevant articles and documents

Using Small Molecules to Enhance P450 OleT Enzyme Activity in Situ

Cytochrome P450 OleT is a fatty acid decarboxylase that catalyzes the production of olefins with biofuel and synthetic applications. However, the relatively sluggish catalytic efficiency of the enzyme limits its applications. Here, we report the application of a novel class of benzene containing small molecules to improve the OleT activity. The UV-Vis spectroscopy study and molecular docking results confirmed the high proximity of the small molecules to the heme group of OleT. Up to 6-fold increase of product yield has been achieved in the small molecule-modulated enzymatic reactions. Our work thus sheds the light to the application of small molecules to increase the OleT catalytic efficiency, which could be potentially used for future olefin productions.

Method for preparing chiral amino compound and intermediate thereof

The invention discloses a method for preparing a chiral amino compound and intermediate thereof. The method comprises the step of performing a deprotection reaction as shown in the specification on acompound in a formula D and mercaptide in a solvent, wherein in the compound in the formula D, X is selected from O or NMe; Y is Me when X is O, and Y is H when X is NMe; n is selected from 0, 1, 2, 3, 4 or 5; each R is independently NO2 or CN; the mercaptide is salt formed by thiol and metal, and is shown as RS-M; M is an alkali metal ion, and is especially selected from one or more of Li, Na, K, Ru and Cs; and R is C14-24 alkyl. The preparation method is simple and convenient to operate, has mild reaction conditions, high yield and high product quality, and is applicableto industrial production.

Oxidative debenzylation of N-benzyl amides and O-benzyl ethers using alkali metal bromide

The oxidative debenzylation of N-benzyl amides and O-benzyl ethers was promoted with high efficiency by a bromo radical formed through the oxidation of bromide from alkali metal bromide under mild conditions. This reaction provided the corresponding amides from N-benzyl amides and carbonyl compounds from O-benzyl ethers in high yields.