620627-46-5

Basic information

• Product Name: (R)-N-(2-HYDROXY-2-METHYL-1-PHENYL-PROPYL)-4-METHYL-BENZENESULFONAMIDE
• Synonyms: N-(2-hydroxy-2-methyl-1-phenylpropyl)-4-methylbenzenesulfonamide;(R)-N-(2-Hydroxy-2-methyl-1-phenyl-propyl)-4-methyl-benzenesulfomide;Benzenesulfonamide, N-[(1R)-2-hydroxy-2-methyl-1-phenylpropyl]-4-methyl-
• CAS NO: 620627-46-5
• Molecular Formula: C₁₇H₂₁NO₃S
• Molecular Weight: 319.42
• Mol File: 620627-46-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 484°C at 760 mmHg
• Flash Point: 246.5°C
• Appearance: /
• Density: 1.206g/cm³
• Vapor Pressure: 3.53E-10mmHg at 25°C
• Refractive Index: 1.583
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (R)-N-(2-HYDROXY-2-METHYL-1-PHENYL-PROPYL)-4-METHYL-BENZENESULFONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-N-(2-HYDROXY-2-METHYL-1-PHENYL-PROPYL)-4-METHYL-BENZENESULFONAMIDE(620627-46-5)
• EPA Substance Registry System: (R)-N-(2-HYDROXY-2-METHYL-1-PHENYL-PROPYL)-4-METHYL-BENZENESULFONAMIDE(620627-46-5)

Safety Data

• Hazardous Substances Data: 620627-46-5(Hazardous Substances Data)

Usage

General Description

The chemical (R)-N-(2-HYDROXY-2-METHYL-1-PHENYL-PROPYL)-4-METHYL-BENZENESULFONAMIDE, also known as Nitenpyram, is an insecticide and pesticide commonly used to control and eliminate pests such as fleas and ticks in pets. It belongs to the class of neonicotinoid chemicals, which target the nervous system of insects, leading to paralysis and ultimately death. Nitenpyram is available in various formulations including tablets, sprays, and spot-on treatments, and is widely used in veterinary medicine and agricultural practices. While effective in targeting pests, it is important to carefully follow safety instructions and guidelines for use to minimize potential harm to non-target organisms and the environment.

InChI:InChI=1/C17H21NO3S/c1-13-9-11-15(12-10-13)22(20,21)18-16(17(2,3)19)14-7-5-4-6-8-14/h4-12,16,18-19H,1-3H3/t16-/m1/s1

Upstream product

• 620627-47-6 (2S,4R)-5,5-dimethyl-4-phenyl-N-tosyl-1,2,3-oxathiazolidine 2-oxide 
• 36321-90-1 2-methoxy-1-naphthylmagnesium bromide 
• 2633-66-1 2-mesitylmagnesium bromide 
• 82214-69-5 2-biphenylmagnesium bromide 
• 1310105-98-6 C₂₁H₂₉NO₄S₂ 
• 1310105-60-2 C₃₂H₄₃NO₄S₂ 
• 24461-61-8 (R)-Phenylglycine methyl ester 
• 111047-53-1 (R)-2-phenylglycine methyl ester hydrochloride salt 
• 75-16-1 methylmagnesium bromide 
• 98-59-9 p-toluenesulfonyl chloride 
• 147-71-7 D-tartaric acid 

Downstream Products

• 620627-47-6 (2S,4R)-5,5-dimethyl-4-phenyl-N-tosyl-1,2,3-oxathiazolidine 2-oxide 
• 1310105-98-6 C₂₁H₂₉NO₄S₂ 
• 247089-85-6 (R)-p-toluenesulfinamide 

Relevant articles and documents

Enantioselective synthesis of diverse sulfinamides and sulfinylferrocenes from phenylglycine-derived chiral sulfinyl transfer agent

A new chiral sulfinyl transfer auxiliary derived from readily available phenylglycine was developed. This auxiliary is utilized to synthesize a diverse array of alkyl- and arylsulfinamides and sulfinylferrocenes in high yields and excellent ee's. The desired products are produced in a one-pot sequence from the oxathiazolidine 2-oxide by two sequential nucleophilic additions that proceed in a stereospecific manner.