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2-Thiazolecarboximidamide is a chemical compound characterized by the molecular formula C4H5N3S. It is a derivative of thiazole, featuring a carboximidamide functional group. 2-Thiazolecarboximidamide is known for its unique chemical structure and properties, which contribute to its value in a range of chemical and pharmaceutical applications.

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  • 212558-27-5 Structure
  • Basic information

    1. Product Name: 2-Thiazolecarboximidamide
    2. Synonyms: 2-Thiazolecarboximidamide;1,3-thiazole-2-carboxiMidaMide;Thiazole-2-carboxiMidaMide;EOS-60666
    3. CAS NO:212558-27-5
    4. Molecular Formula: C4H5N3S
    5. Molecular Weight: 127.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 212558-27-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 243.5±23.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.57±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 10.48±0.50(Predicted)
    10. CAS DataBase Reference: 2-Thiazolecarboximidamide(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Thiazolecarboximidamide(212558-27-5)
    12. EPA Substance Registry System: 2-Thiazolecarboximidamide(212558-27-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 212558-27-5(Hazardous Substances Data)

212558-27-5 Usage

Uses

Used in Pharmaceutical Industry:
2-Thiazolecarboximidamide is utilized as a building block for the synthesis of various drugs and pharmaceutical intermediates. Its presence in the development process is crucial for creating new medicinal compounds that address specific health concerns.
Used in Agricultural Chemical Production:
2-Thiazolecarboximidamide also finds application in the production of agricultural chemicals, where it contributes to the formulation of products designed to enhance crop protection and yield.
Used as a Reagent in Organic Synthesis:
2-Thiazolecarboximidamide serves as a reagent in organic synthesis, facilitating various chemical reactions that are essential for creating complex organic molecules.
Target Molecule for Drug Design and Development:
Due to its potential biological activities, 2-Thiazolecarboximidamide can be employed as a target molecule for drug design and development. Researchers can leverage its properties to create new therapeutic agents that may have beneficial effects on human health.

Check Digit Verification of cas no

The CAS Registry Mumber 212558-27-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,5,5 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 212558-27:
(8*2)+(7*1)+(6*2)+(5*5)+(4*5)+(3*8)+(2*2)+(1*7)=115
115 % 10 = 5
So 212558-27-5 is a valid CAS Registry Number.

212558-27-5Upstream product

212558-27-5Relevant articles and documents

NOVEL 4-METHYL-DIHYDROPYRIMIDINES FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION

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Page/Page column 59-61, (2013/10/21)

The invention provides novel compounds having the general formula (I): wherein R1, R2, R3, R4, R5, M and X are as described herein, compositions including the compounds and methods of using the compounds.

NOVEL 4-METHYL-DIHYDROPYRIMIDINES FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION

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Paragraph 0374, (2013/10/22)

The invention provides novel compounds having the general formula: wherein R1, R2, R3, R4, R5, M and X are as described herein, compositions including the compounds and methods of using the compounds.

Novel synthesis of heterocyclic aryl amidines

Tommasi, Ruben A.,Macchia, William M.,Parker, David T.

, p. 5947 - 5950 (2007/10/03)

We have developed a novel amidine synthesis that allows the preparation of heterocyclic amidines that were previously unknown and difficult to prepare by published methods. The route involves the lithiation of heterocycles by the action of n-BuLi followed

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