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2-Aminopyrimidine-5-carbonitrile is an organic compound with the molecular formula C5H4N4. It is a heterocyclic compound featuring a pyrimidine ring with an amino group at the 2nd position and a carbonitrile group at the 5th position. 2-Aminopyrimidine-5-carbonitrile serves as an important intermediate in the synthesis of various pharmaceuticals and bioactive molecules due to its unique chemical structure and reactivity.

1753-48-6

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1753-48-6 Usage

Uses

Used in Pharmaceutical Industry:
2-Aminopyrimidine-5-carbonitrile is used as a key intermediate for the synthesis of pyrazinone and pyridinone derivatives, which are known as thrombin inhibitors. Thrombin inhibitors play a crucial role in the treatment of various medical conditions, such as coagulation disorders, thrombosis, and stroke, by preventing the clotting of blood and reducing the risk of blood clot formation.
The compound's utility in the pharmaceutical industry lies in its ability to be further modified and functionalized to develop novel thrombin inhibitors with improved potency, selectivity, and pharmacokinetic properties. This makes 2-Aminopyrimidine-5-carbonitrile a valuable building block for the design and development of innovative therapeutic agents targeting thrombin-mediated diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 1753-48-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,5 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1753-48:
(6*1)+(5*7)+(4*5)+(3*3)+(2*4)+(1*8)=86
86 % 10 = 6
So 1753-48-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H4N4/c6-1-4-2-8-5(7)9-3-4/h2-3H,(H2,7,8,9)

1753-48-6SDS

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 2-Aminopyrimidine-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-Aminopyrimidine-5-Carbonitrile

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:1753-48-6 SDS

1753-48-6Relevant academic research and scientific papers

ORGANIC FLUORESCENT LUMINESCENT MATERIAL AND ORGANIC ELECTROLUMINESCENT DEVICE

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Paragraph 0041, (2017/07/06)

An organic fluorescent luminescent material and an organic electro-luminescence device are provided. The organic fluorescent luminescent material may be represented by the formula, (Ar)-(Ph)-(X), wherein Ar is Ph include at least one benzene ring, X is a six-membered aromatic ring, and at least one nitrogen atom is located on the six-membered aromatic ring. The organic fluorescent luminescent material can be used in organic electro-luminescence devices.

Non-covalent thrombin inhibitors featuring P3-heterocycles with P1-monocyclic arginine surrogates

Reiner, John E.,Siev, Daniel V.,Araldi, Gian-Luca,Cui, Jingrong Jean,Ho, Jonathan Z.,Reddy, Komandla Malla,Mamedova, Lala,Vu, Phong H.,Lee, Kuen-Shan S.,Minami, Nathaniel K.,Gibson, Tony S.,Anderson, Susanne M.,Bradbury, Annette E.,Nolan, Thomas G.,Semple, J. Edward

, p. 1203 - 1208 (2007/10/03)

Investigations on P2-P3-heterocyclic dipeptide surrogates directed towards identification of an orally bioavailable thrombin inhibitor led us to pursue novel classes of achiral, non-covalent P1-arginine derivatives. The design, synthesis, and biological activity of inhibitors NC1-NC30 that feature three classes of monocyclic P1-arginine surrogates will be disclosed: (1) (hetero)aromatic amidines, amines and hydroxyamidines, (2) 2-aminopyrazines, and (3) 2-aminopyrimidines and 2-aminotetrahydropyrimidines.

SYNTHESIS WITH NITRILES: 92. SYNTHESIS OF 5-FORMYLCYTOSINE DERIVATIVES

Jachak, Madhukar,Mittelbach, Martin,Junek, Hans

, p. 2281 - 2290 (2007/10/02)

The reactivity of 3-dimethylamino-2-formylpropenenitrile (1) with various amino compounds is studied.Thus, condensation of 1 with anilines gives the corresponding azomethines (2a-c).Reaction of 1 with thiourea and guanidine resp., leads to 5-formylthiocyt

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