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1H-Indazole, 5-methyl-7-nitro-, also known as 5-Methyl-7-nitroindazole, is a heterocyclic chemical compound belonging to the indazole class. It is characterized by the presence of a methyl group at the 5th position and a nitro group at the 7th position in the indazole ring. This unique structure and properties make it a valuable compound for research and experimentation in organic chemistry and drug discovery. The nitro group in the molecule offers potential for further functionalization and modification, leading to the development of novel compounds with diverse biological activities and pharmaceutical capabilities.

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  • 113302-88-8 Structure
  • Basic information

    1. Product Name: 1H-Indazole, 5-Methyl-7-nitro-
    2. Synonyms: 1H-Indazole, 5-Methyl-7-nitro-;5-Methyl-7-nitro-1H-indazole
    3. CAS NO:113302-88-8
    4. Molecular Formula: C8H7N3O2
    5. Molecular Weight: 177.16008
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 113302-88-8.mol
  • Chemical Properties

    1. Melting Point: 191-192 °C
    2. Boiling Point: 397.2±22.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.437±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 10.25±0.40(Predicted)
    10. CAS DataBase Reference: 1H-Indazole, 5-Methyl-7-nitro-(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1H-Indazole, 5-Methyl-7-nitro-(113302-88-8)
    12. EPA Substance Registry System: 1H-Indazole, 5-Methyl-7-nitro-(113302-88-8)
  • 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: 113302-88-8(Hazardous Substances Data)

113302-88-8 Usage

Uses

Used in Pharmaceutical Industry:
1H-Indazole, 5-methyl-7-nitrois used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a promising candidate for the development of new drugs and medicines with potential therapeutic applications.
Used in Organic Chemistry Research:
1H-Indazole, 5-methyl-7-nitroserves as a valuable tool for researchers in the field of organic chemistry. Its unique structure allows for further functionalization and modification, enabling the synthesis of novel compounds with various biological activities. 1H-Indazole, 5-methyl-7-nitrocan be used to explore new reaction pathways and develop innovative synthetic methods.
Used in Drug Discovery:
The potential applications of 1H-Indazole, 5-methyl-7-nitroin the pharmaceutical industry make it an attractive candidate for drug discovery. Its unique structure and properties can be leveraged to design and develop new drugs with improved efficacy, selectivity, and safety profiles. The nitro group in the molecule can be further modified to explore its impact on the biological activity and pharmaceutical capabilities of the resulting compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 113302-88-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,0 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 113302-88:
(8*1)+(7*1)+(6*3)+(5*3)+(4*0)+(3*2)+(2*8)+(1*8)=78
78 % 10 = 8
So 113302-88-8 is a valid CAS Registry Number.

113302-88-8Relevant articles and documents

TYK2 INHIBITORS AND USES THEREOF

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Paragraph 00410, (2020/09/27)

Described herein are compounds that are useful in treating a TYK2-mediated disorder. In some embodiments, the TYK2-mediated disorder is an autoimmune disorder, an inflammatory disorder, a proliferative disorder, an endocrine disorder, a neurological disorder, or a disorder associated with transplantation.

Indole and indazole compounds as an inhibitor of cellular necrosis

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Paragraph 0408-0410, (2016/10/08)

The present invention refers to a formula (1) compounds of, pharmaceutically acceptable salts or isomers thereof thereof, and characterized by by containing as active ingredients-associated diseases, cell death and method for the prevention or treatment of relates and compositions. [Formula 1] In formula said R 1, R 2, R 3, R 4, R 5, R 6, A, X, n and m to equal the specification.

INDOLE AND INDAZOLE COMPOUNDS AS AN INHIBITOR OF CELLULAR NECROSIS

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Page/Page column 15, (2010/08/08)

The present invention relates to indole or indazole compounds, pharmaceutically acceptable salts or isomers thereof which are useful for the prevention or treatment of cellular necrosis and necrosis-associated diseases. The present invention also relates to a method and a composition for the prevention or treatment of cellular necrosis and necrosis-associated diseases, comprising said indole or indazole compounds as an active ingredient.

INDOLE AND INDAZOLE COMPOUNDS AS AN INHIBITOR OF CELLULAR NECROSIS

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Page/Page column 33; 53, (2009/04/25)

The present invention relates to indole or indazole compounds, pharmaceutically acceptable salts or isomers thereof which are useful for the prevention or treatment of cellular necrosis and necrosis-associated diseases. The present invention also relates to a method and a composition for the prevention or treatment of cellular necrosis and necrosis-associated diseases, comprising said indole or indazole compounds as an active ingredient.

Synthesis and Complexing Properties of Macrocycles Incorporating 2,2'-Biindazolyl Binding Subunits

Cuevas, Juan C.,Mendoza, Javier de,Prados, Pilar

, p. 2055 - 2066 (2007/10/02)

Substituted 2,2'-biindazoles 4 and 19-23 were prepared in 80-90percent yields by thermal decomposition of o,o'-diazido azines 13-18, which in turn were readily obtained from the corresponding 2-azidobenzaldehydes or 2-azidobenzophenones.The preference of

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