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1036959-27-9

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1036959-27-9 Usage

Description

(2R)-1-[2-[(3-Hydroxytricyclo[3.3.1.1(3,7)]dec-1-yl)amino]acetyl]-2-pyrrolidinecarbonitrile is a complex organic compound with a unique molecular structure. It is characterized by its tricyclic core, hydroxyl and amino functional groups, and a pyrrolidinecarbonitrile moiety. (2R)-1-[2-[(3-Hydroxytricyclo[3.3.1.1(3,7)]dec-1-yl)amino]acetyl]-2-pyrrolidinecarbonitrile has potential applications in various fields due to its structural diversity and functional groups.

Uses

Used in Pharmaceutical Industry:
(2R)-1-[2-[(3-Hydroxytricyclo[3.3.1.1(3,7)]dec-1-yl)amino]acetyl]-2-pyrrolidinecarbonitrile is used as a pharmaceutical compound for its potential therapeutic properties. The compound's unique structure and functional groups may allow it to interact with specific biological targets, making it a candidate for the development of new drugs.
Used in Antidiabetic Applications:
In the field of antidiabetic research, (2R)-1-[2-[(3-Hydroxytricyclo[3.3.1.1(3,7)]dec-1-yl)amino]acetyl]-2-pyrrolidinecarbonitrile may be utilized as an oral anti-hyperglycemic agent. It could potentially inhibit dipeptidyl peptidase 4 (DPP-4), a serine exopeptidase, which plays a role in the regulation of glucose levels in the body. By targeting DPP-4, this compound may help manage blood sugar levels and provide additional cardiovascular and anti-inflammatory benefits for patients with type 2 diabetes.
Used in Drug Delivery Systems:
(2R)-1-[2-[(3-Hydroxytricyclo[3.3.1.1(3,7)]dec-1-yl)amino]acetyl]-2-pyrrolidinecarbonitrile may also be employed in the development of novel drug delivery systems. Its structural features could be exploited to enhance the delivery, bioavailability, and therapeutic outcomes of various drugs, particularly in the context of cancer treatment. By incorporating this compound into drug delivery platforms, researchers may be able to improve the efficacy and safety of existing treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 1036959-27-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,9,5 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1036959-27:
(9*1)+(8*0)+(7*3)+(6*6)+(5*9)+(4*5)+(3*9)+(2*2)+(1*7)=169
169 % 10 = 9
So 1036959-27-9 is a valid CAS Registry Number.

1036959-27-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name vildagliptin

1.2 Other means of identification

Product number -
Other names (2R)-Vildagliptin

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:1036959-27-9 SDS

1036959-27-9Downstream Products

1036959-27-9Relevant articles and documents

Tubular reaction continuous preparation of vergeliptin method and device

-

Paragraph 0032-0041, (2017/08/04)

The invention relates to a method and a device for continuous preparation of Vildagliptin by tubular reaction; 3-amino-1-adamantanol and 1-chloracetyl-2-cyano pyrrolidine are dissolved in a mixed solution of solvents, then dissolved with an alkali and a catalyst in a suspension of the solvents, mixed, and preheated by a preheater, the preheated mixed solution enters into a tubular reactor at 20-100 DEG C, the residence time of a material in the tubular reactor is 30min-180min, and the reaction solution discharged from the tubular reactor is collected, filtered washed and purified to obtain the product. The method greatly improves the response speed, shortens the production cycle, increases the amount of processing, and can effectively improve the production capacity. In addition, by controlling the reaction temperature, material movement speed, dosage ratio, catalyst amount and alkali dosage, the formation of by-products disubstituted compounds can be effectively avoided.

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