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1092578-48-7

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1092578-48-7 Usage

Description

3-((3S,4R)-4-Methyl-3-(Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidin-1-yl)-3-oxopropanenitrile is a complex organic compound with a unique molecular structure. It is characterized by its stereochemistry, with the 3S,4R configuration, and its functional groups, including a piperidine ring, a pyrimidine ring, and a cyano group. 3-((3S,4R)-4-Methyl-3-(Methyl(7H-pyrrolo[2,3-d]pyriMidin-4-yl)aMino)piperidin-1-yl)-3-oxopropanenitrile has potential applications in various fields due to its structural features and biological activities.

Uses

Used in Pharmaceutical Industry:
3-((3S,4R)-4-Methyl-3-(Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidin-1-yl)-3-oxopropanenitrile is used as a pharmaceutical compound for its potential therapeutic effects. The compound's unique structure and functional groups may allow it to interact with specific biological targets, such as enzymes or receptors, which could lead to the development of new drugs for various diseases.
Used in Research and Development:
In the field of research and development, 3-((3S,4R)-4-Methyl-3-(Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidin-1-yl)-3-oxopropanenitrile can be used as a starting material or a building block for the synthesis of more complex molecules with potential applications in various industries, such as pharmaceuticals, agrochemicals, and materials science.
Used in Enzyme Inhibition:
3-((3S,4R)-4-Methyl-3-(Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidin-1-yl)-3-oxopropanenitrile may be used as an enzyme inhibitor, particularly for Janus kinase 3 (Jak3), as it is structurally similar to the drug tofacitinib, which is a known Jak3 inhibitor. By inhibiting specific kinases, this compound could potentially be used to treat conditions related to the dysregulation of these enzymes, such as autoimmune diseases or cancer.
Used in Drug Delivery Systems:
Similar to gallotannin, 3-((3S,4R)-4-Methyl-3-(Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidin-1-yl)-3-oxopropanenitrile could be incorporated into drug delivery systems to improve its bioavailability, delivery, and therapeutic outcomes. By using various organic and metallic nanoparticles as carriers, the compound's efficacy against specific targets could be enhanced, leading to improved treatment options for various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 1092578-48-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,5,7 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1092578-48:
(9*1)+(8*0)+(7*9)+(6*2)+(5*5)+(4*7)+(3*8)+(2*4)+(1*8)=177
177 % 10 = 7
So 1092578-48-7 is a valid CAS Registry Number.

1092578-48-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(3S,4R)-4-methyl-3-[methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]piperidin-1-yl]-3-oxopropanenitrile

1.2 Other means of identification

Product number -
Other names (3S,4R)-Tofacitinib

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:1092578-48-7 SDS

1092578-48-7Downstream Products

1092578-48-7Relevant articles and documents

Preparation method and application of chiral amine B

-

, (2019/06/05)

The invention discloses a preparation method of chiral amine B. The preparation method comprises the following steps: (1) carrying out nucleophilic substitution reaction on N-tert-butoxycarbonyl-3-pyridine and halogenated benzyl to obtain an intermediate

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