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6,7-difluoro-1H-Indazol-3-amine is a chemical compound belonging to the class of organic compounds known as indazoles. These are aromatic heterocyclic compounds characterized by a benzene ring fused to an azazole ring. The presence of a nitrogen atom and two fluorine atoms in its structure endows this compound with unique properties that may be valuable for scientific research. However, detailed information about its physical properties, toxicity, hazards, uses, or role in biological systems is currently limited, suggesting that it is likely used in highly specific scientific studies and its properties are still under investigation.

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  • 706805-37-0 Structure
  • Basic information

    1. Product Name: 6,7-difluoro-1H-Indazol-3-amine
    2. Synonyms: 6,7-difluoro-1H-Indazol-3-amine;3-Amino-6,7-difluoro-1H-indazole
    3. CAS NO:706805-37-0
    4. Molecular Formula: C7H5F2N3
    5. Molecular Weight: 169
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 706805-37-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    8. Solubility: N/A
    9. CAS DataBase Reference: 6,7-difluoro-1H-Indazol-3-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6,7-difluoro-1H-Indazol-3-amine(706805-37-0)
    11. EPA Substance Registry System: 6,7-difluoro-1H-Indazol-3-amine(706805-37-0)
  • 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: 706805-37-0(Hazardous Substances Data)

706805-37-0 Usage

Uses

Due to the limited information available about 6,7-difluoro-1H-Indazol-3-amine, its applications are not well-defined. However, based on its classification as an indazole derivative, it can be inferred that it may be used in the following ways:
Used in Pharmaceutical Research:
6,7-difluoro-1H-Indazol-3-amine is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, including the presence of fluorine atoms, may contribute to the development of new drugs with improved properties, such as increased potency, selectivity, or bioavailability.
Used in Chemical Synthesis:
6,7-difluoro-1H-Indazol-3-amine is used as a building block in the synthesis of more complex organic molecules. Its reactivity and the presence of functional groups may facilitate the formation of new chemical entities with potential applications in various fields, such as materials science, agrochemistry, or specialty chemicals.
Used in Material Science:
6,7-difluoro-1H-Indazol-3-amine is used as a component in the development of novel materials with specific properties. The incorporation of this compound into polymers or other materials may result in materials with enhanced thermal stability, electrical conductivity, or other desirable characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 706805-37-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,6,8,0 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 706805-37:
(8*7)+(7*0)+(6*6)+(5*8)+(4*0)+(3*5)+(2*3)+(1*7)=160
160 % 10 = 0
So 706805-37-0 is a valid CAS Registry Number.
InChI:InChI=1S/C7H5F2N3/c8-4-2-1-3-6(5(4)9)11-12-7(3)10/h1-2H,(H3,10,11,12)

706805-37-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,7-difluoro-1H-indazol-3-amine

1.2 Other means of identification

Product number -
Other names 6,7-difluoro-1H-indazole-3-amine

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:706805-37-0 SDS

706805-37-0Downstream Products

706805-37-0Relevant articles and documents

Rational design of potent GSK3β inhibitors with selectivity for Cdk1 and Cdk2

Lesuisse, Dominique,Dutruc-Rosset, Gilles,Tiraboschi, Gilles,Dreyer, Matthias K.,Maignan, Sébastien,Chevalier, Alain,Halley, Frank,Bertrand, Philippe,Burgevin, Marie-Claude,Quarteronet, Dominique,Rooney, Thomas

scheme or table, p. 1985 - 1989 (2010/08/06)

From an HTS hit, a series of potent and selective inhibitors of GSK3β have been designed based on a Cdk2-homology model and with the help of several crystal structures of the compounds within Cdk2.

Aminoindazole derivatives and intermediates, preparation thereof, and pharmaceutical compositions thereof

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Page/Page column 27, (2010/11/30)

The present invention relates to the novel indazole derivatives of general formula (I): in which: R is either O, S or NH; R3 is an alkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, aryl, heterocycle, cycloalkyl, alkenyl, etc. radical; these radicals being optionally substituted with one or more substituents; R4, R5, R6 and R7 are chosen, independently of each other, from the following radicals: hydrogen, halogen, CN, NO2, NH2, OH, COOH, C(O)OR8, —O—C(O)R8, NR8R9, NHC(O)R8, C(O)NR8R9, NHC(S)R8, C(S)NR8R9, SR8, S(O)R8, SO2R8, NHSO2R8, SO2NR8R9, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, aryl, arylalkyl, heteroaryl, heteroarylalkyl, heterocycle, cycloalkyl, alkenyl, etc.; these radicals being optionally substituted with one or more substituents.

Novel aminoindazole derivatives as medicaments and pharmaceutical compositions including them

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Page/Page column 12, (2008/06/13)

The present invention relates to novel derivatives of general formula (I) in which R3 is a (1-6C)alkyl, aryl, aryl(1-6C)alkyl, heteroaryl, heteroaryl(1-6C)alkyl, aryl or heteroaryl fused to a (1-10C) cycloalkyl, heterocycle, heterocycloalkyl, cycloalkyl,

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