Cookies disclaimer

I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.

H27724 (R)-(+)-2-Methyl-2-propanesulfinamide, 98%

CAS Number
196929-78-9
Synonyms
(R)-(+)-tert-Butyl sulfinamide

Stock No. Size Price ($) Quantity Availability
H27724-03 1g 66.10
H27724-06 5g 223.00
H27724-14 25g 762.00
Add to Cart Bulk/Specialty Print Quote View Item

(R)-(+)-2-Methyl-2-propanesulfinamide, 98%

MDL
MFCD05861479

Chemical Properties

Formula
C4H11NOS
Formula Weight
121.20
Melting point
ca 100-105°
Storage & Sensitivity
Keep Cold.
Solubility
Soluble in chloroform, methanol, tetrahydrofuran, dichloromethane, dimethyl sulfoxide and most organic solvents.

Applications

(R)-(+)-2-Methyl-2-propanesulfinamide is a chiral ligand, which is used in pharmaceutical compositions. Further, it is used in the preparation of beta-chloro sulfinamides in the synthesis of chiral azridines. It is involved in the preparation of organocatalyst for enantioselective reduction of imines. It serves as a reagent for synthesizing chiral amines. In addition to this, it is converted into P,N-sulfinyl imine ligands through condensation with aldehydes and ketones which undergoes iridium-catalyzed asymmetric hydrogenation of olefins.

Notes

Incompatible with strong oxidizing agents, strong acids and bases. Store in a cool place.

Literature References

Qian, X.; Tang, E.; Fan, J.; Zhu, K.; Zhu, J.; Shabaker, J.; Lo, E.; Malley, M.; Deshpande, R. A stereoselective synthesis of (S)-2-(((3-fluoro-4-methylphenoxy)carbonyl)(1-(4-((5-methyl-2-phenyloxazol-4-yl)methoxy)phenyl)ethyl)amino)acetic acid, a highly potent PPAR alpha/gamma dual agonist. Tetrahedron 2015, 71 (50), 9408-9414.

Bender, A. M.; Griggs, N. W.; Anand, J. P.; Traynor, J. R.; Jutkiewicz, E. M.; Mosberg, H. I. Asymmetric Synthesis and in Vitro and in Vivo Activity of Tetrahydroquinolines Featuring a Diverse Set of Polar Substitutions at the 6 Position as Mixed-Efficacy mu Opioid Receptor/delta Opioid Receptor Ligands. ACS Chem. Neurosci. 2015, 6 (8), 1428-1435.

GHS Hazard and Precautionary Statements

Hazard Statements: H315-H319-H335

Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.

Precautionary Statements: P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P501c

Avoid breathing dust/fume/gas/mist/vapours/spray. Wash face, hands and any exposed skin thoroughly after handling Use only outdoors or in a well-ventilated area. Wear protective gloves/protective clothing/eye protection/face protection. IF ON SKIN: Wash with plenty of soap and water. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Call a POISON CENTER or doctor/physician if you feel unwell. If skin irritation occurs: Get medical advice/attention. If eye irritation persists: Take off contaminated clothing and wash before reuse. Dispose of contents/ container to an approved waste disposal plant

Other References

Harmonized Tariff Code
2930.90
TSCA
No

Recommended

Recently Viewed

Chemicals

Life Science

Metals & Materials

Catalysts

Analytical & Labware