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1071435-61-4

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1071435-61-4 Usage

Description

(1R)-1-[6-(TRIFLUOROMETHYL)(3-PYRIDYL)]ETHYLAMINE, also known as (R)-6-(trifluoromethyl)nicotine, is a chiral amine with the molecular formula C8H10F3N. It is a derivative of nicotine that has been modified to contain a trifluoromethyl group. (1R)-1-[6-(TRIFLUOROMETHYL)(3-PYRIDYL)]ETHYLAMINE is commonly used in organic synthesis and pharmaceutical research, and is often utilized as a building block in the synthesis of various pharmaceuticals and agrochemicals.
Used in Pharmaceutical Research:
(1R)-1-[6-(TRIFLUOROMETHYL)(3-PYRIDYL)]ETHYLAMINE is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and properties make it a valuable component in the development of new synthetic methods and compounds.
Used in Organic Synthesis:
(1R)-1-[6-(TRIFLUOROMETHYL)(3-PYRIDYL)]ETHYLAMINE is used as a key intermediate in organic synthesis, allowing for the creation of a wide range of chemical compounds.
Used in Drug Development:
(1R)-1-[6-(TRIFLUOROMETHYL)(3-PYRIDYL)]ETHYLAMINE is used as a potential drug lead compound for the treatment of various diseases, due to its nicotine-like properties and potential biological activity.
Used in the Development of New Synthetic Methods:
(1R)-1-[6-(TRIFLUOROMETHYL)(3-PYRIDYL)]ETHYLAMINE is used in the development of new synthetic methods, as its unique structure and properties allow for innovative approaches in chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 1071435-61-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,1,4,3 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1071435-61:
(9*1)+(8*0)+(7*7)+(6*1)+(5*4)+(4*3)+(3*5)+(2*6)+(1*1)=124
124 % 10 = 4
So 1071435-61-4 is a valid CAS Registry Number.

1071435-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R)-1-[6-(trifluoromethyl)pyridin-3-yl]ethanamine

1.2 Other means of identification

Product number -
Other names -

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:1071435-61-4 SDS

1071435-61-4Relevant articles and documents

CARBAMATE DERIVATIVES AND USES THEREOF

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Paragraph 01340; 01354; 01392-01393, (2020/08/13)

The present disclosure relates to compounds of Formula (I): and to their prodrugs, pharmaceutically acceptable salts, pharmaceutical compositions, methods of use, and methods for their preparation. The compounds disclosed herein are useful for inhibiting the maturation of cytokines of the IL-1 family by inhibiting inflammasomes and may be used in the treatment of disorders in which inflammasome activity is implicated, such as inflammatory, autoinflammatory and autoimmune diseases and cancers.

Asymmetric Biocatalytic Synthesis of Fluorinated Pyridines through Transesterification or Transamination: Computational Insights into the Reactivity of Transaminases

López-Iglesias, María,González-Martínez, Daniel,Rodríguez-Mata, María,Gotor, Vicente,Busto, Eduardo,Kroutil, Wolfgang,Gotor-Fernández, Vicente

, p. 279 - 291 (2017/02/05)

The synthesis of a family of pyridines bearing a fluorinated substituent on the aromatic ring has been carried out through two independent and highly stereoselective chemoenzymatic strategies. Short chemical synthetic routes toward fluorinated racemic amines and prochiral ketones have been developed, which served as substrates to explore the suitability of lipases and transaminases in asymmetric biotransformations. The lipase-catalyzed kinetic resolution via acylation of racemic amines proceeded smoothly giving conversions close to 50% and excellent enantioselectivities. Alternatively, the biotransamination of the corresponding prochiral ketones was investigated giving access to both optically pure amine enantiomers using transaminases with complementary selectivity. High to quantitative conversion values were achieved, which allowed the isolation of the amines in moderate to high yields (40–88%). A deeper understanding of the latter process was enabled by performing theoretical calculations on thermodynamic and mechanistic aspects. Calculations showed that the biotransamination reactions are highly favoured by the presence of fluorine atoms and the pyridine ring. (Figure presented.).

2-Cyanophenyl fused heterocyclic compounds, and compositions and uses thereof

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Page/Page column 26, (2008/12/08)

Fused heterocyclic compounds are provided according to formula 1: where R1, R2, R3, and m are as defined herein. Provided compounds and pharmaceutical compositions thereof are useful for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, pain, inflammation, cognitive disorders, anxiety, depression, and others.

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