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1789703-37-2

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1789703-37-2 Usage

Description

2-(3-hydroxyadamantan-1-yl)-1-imino-hexahydropyrrolo[1,2-a]pyrazin-4-one is a complex organic compound with a unique molecular structure. It is characterized by its hexahydropyrrolo[1,2-a]pyrazin-4-one core, which is adorned with a 3-hydroxyadamantan-1-yl group and an imino functional group. 2-(3-hydroxyadamantan-1-yl)-1-imino-hexahydropyrrolo[1,2-a]pyrazin-4-one holds potential for various applications due to its distinct chemical properties and interactions with biological systems.

Uses

Used in Pharmaceutical Industry:
2-(3-hydroxyadamantan-1-yl)-1-imino-hexahydropyrrolo[1,2-a]pyrazin-4-one is used as a pharmaceutical compound for its potential therapeutic effects. The compound's unique structure allows it to interact with specific biological targets, making it a candidate for the development of new drugs to treat various diseases.
Used in Antidiabetic Applications:
In the context of type 2 diabetes, 2-(3-hydroxyadamantan-1-yl)-1-imino-hexahydropyrrolo[1,2-a]pyrazin-4-one is used as an antidiabetic agent. It may function by inhibiting DPP-4, a serine exopeptidase, which plays a role in the regulation of blood glucose levels. By inhibiting this enzyme, the compound could help improve glycemic control and provide additional cardiovascular and anti-inflammatory benefits.
Used in Drug Delivery Systems:
Similar to gallotannin, 2-(3-hydroxyadamantan-1-yl)-1-imino-hexahydropyrrolo[1,2-a]pyrazin-4-one may also be employed in drug delivery systems to enhance its bioavailability and therapeutic outcomes. The compound could be incorporated into various carriers, such as organic and metallic nanoparticles, to improve its delivery to target cells and tissues, ultimately increasing its efficacy in treating specific conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1789703-37-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,8,9,7,0 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1789703-37:
(9*1)+(8*7)+(7*8)+(6*9)+(5*7)+(4*0)+(3*3)+(2*3)+(1*7)=232
232 % 10 = 2
So 1789703-37-2 is a valid CAS Registry Number.

1789703-37-2Upstream product

1789703-37-2Downstream Products

1789703-37-2Relevant articles and documents

Preparation method of vildagliptin cyclic amidine impurity

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Paragraph 0024; 0025; 0026; 0027; 0028; 0029; 0030-0035, (2018/08/28)

The invention discloses a preparation method of a vildagliptin cyclic amidine impurity. The preparation method comprises the following steps: adding a reaction solvent into vildagliptin (I) and addingalkali; raising the temperature to 30 to 180 DEG C, wherein the reaction time is 2 to 8h; purifying a reaction solution to obtain the vildagliptin cyclic amidine impurity (II). The invention providesa synthesis method of the vildagliptin cyclic amidine impurity for the first time; the vildagliptin is used as a raw material and the vildagliptin cyclic amidine impurity is prepared by adopting one-step ring-forming reaction; the preparation method is moderate in reaction conditions, is easy to operate and high in yield. A product, which accords with quality standards, can be obtained through simple purification and the research and development cost is effectively reduced.

Preparation method of degrading impurities by means of vildagliptin

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Paragraph 0032; 0033; 0034; 0035; 0036; 0037-0054; 0064, (2017/07/19)

The invention relates to the technical field of chemical industry, and discloses a preparation method of degrading impurities by means of vildagliptin. The preparation method comprises the steps that vildagliptin, a first compound and a second compound react to generate N-(3-hydroxyl adamantane)-1-imino-hexahydro-pyrrole[1,2-a]pyrazine-4(1H)-one, wherein the first compound is ethyl acetate or methylbenzene, and the second compound is triethylamine or diisopropylethylamine. According to the preparation method of degrading the impurities by means of vildagliptin, vildagliptin serves as the raw material, appropriate reactants are selected for preparing degradation products of vildagliptin, the technology is simple and convenient, the yield and purity are high, and a basis is provided for controlling the quality standard of pharmaceutical products of vildagliptin.

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