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1219607-85-8

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1219607-85-8 Usage

Description

(r)-2-methyl-n-[(1e)-2,2,2-trifluoroethylidene]propane-2-sulfinamide is an organic compound characterized by the presence of a sulfinamide functional group. It is defined by its chemical formula C6H12F3NO2S and has a molecular weight of 211.227 g/mol. (r)-2-methyl-n-[(1e)-2,2,2-trifluoroethylidene]propane-2-sulfinamide is currently under investigation for its potential applications in chemical research and pharmaceutical development, with a focus on its possible utility in treating various health conditions. Further research is necessary to ascertain its full spectrum of benefits and risks.

Uses

Used in Chemical Research:
(r)-2-methyl-n-[(1e)-2,2,2-trifluoroethylidene]propane-2-sulfinamide is utilized as a research compound for exploring its chemical properties and potential interactions with other substances. Its unique structure, which includes a trifluoroethylidene group and a sulfinamide functional group, makes it an interesting candidate for studying various chemical reactions and mechanisms.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (r)-2-methyl-n-[(1e)-2,2,2-trifluoroethylidene]propane-2-sulfinamide is used as a starting material or intermediate in the synthesis of new drug candidates. Its specific role in drug development is still under investigation, but its unique structural features may contribute to the creation of novel therapeutic agents.
Used in Treatment of Health Conditions:
While still in the research phase, (r)-2-methyl-n-[(1e)-2,2,2-trifluoroethylidene]propane-2-sulfinamide may have potential applications in the treatment of various health conditions. Its use in this context is contingent upon the outcomes of ongoing research, which aims to determine its efficacy, safety, and optimal dosages for potential therapeutic use.

Check Digit Verification of cas no

The CAS Registry Mumber 1219607-85-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,6,0 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1219607-85:
(9*1)+(8*2)+(7*1)+(6*9)+(5*6)+(4*0)+(3*7)+(2*8)+(1*5)=158
158 % 10 = 8
So 1219607-85-8 is a valid CAS Registry Number.

1219607-85-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-N-tert-butanesulfinyl (3,3,3)-trifluoroacetaldimine

1.2 Other means of identification

Product number -
Other names (R)-2-Methyl-N-(2,2,2-trifluoroethylidene)propane-2-sulfinamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1219607-85-8 SDS

1219607-85-8Downstream Products

1219607-85-8Relevant articles and documents

The Ruthenium-Catalyzed Domino Cross Enyne Metathesis/Ring-Closing Metathesis in the Synthesis of Enantioenriched Nitrogen-Containing Heterocycles

Llobat, Alberto,Escorihuela, Jorge,Sedgwick, Daniel M.,Rodenes, Miriam,Román, Raquel,Soloshonok, Vadim A.,Han, Jianlin,Medio-Simón, Mercedes,Fustero, Santos

, p. 4193 - 4207 (2020)

The tetrahydropyridine structure is present in a wide variety of natural and synthetic compounds with interesting pharmacological properties. Therefore, the search for new chemical routes capable of yielding this valuable nitrogen-containing heterocycle is of utmost interest. Herein, we report the use of the ruthenium-catalyzed ring-closing enyne metathesis (RCEYM) and cross enyne metathesis/ring-closing metathesis (CEYM/RCM) reactions of chiral nitrogen-containing 1,7-enynes as an efficient route to synthesize a variety of enantioenriched tetrahydropyridine-based conjugated 1,3-dienes. The RCEYM presented wide functional group tolerance and took place in moderate to high yields, with no significant differences when carried out on gram scale. These 1,3-dienes were suitable for further transformations, such as the Diels–Alder reaction, effectively yielding more complex enantioenriched bicyclic structures.

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