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3-IODO-4-NITRO (1H)INDAZOLE is a chemical compound belonging to the indazole family, characterized by the presence of a nitro group and an iodo substituent. It is known for its unique structural properties and versatile reactivity, making it a valuable tool in the synthesis of various organic compounds and pharmaceuticals. 3-IODO-4-NITRO (1H)INDAZOLE has been studied for its potential as an antimicrobial and antitumor agent due to its ability to inhibit specific biological pathways and processes. However, its potential toxicity and environmental impact require careful handling in research and laboratory settings.

885521-22-2

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  • 4-{[5-(TRIFLUOROMETHYL)-2-PYRIDINYL]-OXY}BENZENESULFONOYL CHLORIDE

    Cas No: 885521-22-2

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885521-22-2 Usage

Uses

Used in Pharmaceutical Industry:
3-IODO-4-NITRO (1H)INDAZOLE is used as a building block or intermediate for the synthesis of various pharmaceuticals. Its unique structural properties and versatile reactivity make it a valuable component in the development of new drugs and materials in the field of medicinal chemistry.
Used in Antimicrobial Applications:
3-IODO-4-NITRO (1H)INDAZOLE is used as an antimicrobial agent for its potential to inhibit specific biological pathways and processes, making it a promising candidate for the development of new antimicrobial drugs.
Used in Antitumor Applications:
3-IODO-4-NITRO (1H)INDAZOLE is used as an antitumor agent due to its ability to inhibit specific biological pathways and processes, showing potential in the development of new cancer treatments.
Used in Research and Laboratory Settings:
3-IODO-4-NITRO (1H)INDAZOLE is used as a research compound in various laboratory settings for the study of its potential applications and properties, including its antimicrobial and antitumor capabilities. Its unique structural properties and versatile reactivity make it a valuable tool for the development of new drugs and materials in the field of chemical biology.

Check Digit Verification of cas no

The CAS Registry Mumber 885521-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,5,2 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 885521-22:
(8*8)+(7*8)+(6*5)+(5*5)+(4*2)+(3*1)+(2*2)+(1*2)=192
192 % 10 = 2
So 885521-22-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H4IN3O2/c8-7-6-4(9-10-7)2-1-3-5(6)11(12)13/h1-3H,(H,9,10)

885521-22-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-iodo-4-nitro-2H-indazole

1.2 Other means of identification

Product number -
Other names 3-iodanyl-4-nitro-2H-indazole

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:885521-22-2 SDS

885521-22-2Upstream product

885521-22-2Relevant articles and documents

SUBSTITUTED N-(1H-INDAZOL-4-YL)IMIDAZO[1,2-a]PYRIDINE-3-CARBOXAMIDE COMPOUNDS AS TYPE III RECEPTOR TYROSINE KINASE INHIBITORS

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Page/Page column 135, (2012/06/30)

Compounds of Formula I: and pharmaceutically acceptable salts thereof in which R1, R2, R3, R4, R5 and R6 have the meanings given in the specification, are inhibitors of cFMS and are useful in the treatment of fibrosis, bone-related diseases, cancer, autoimmune disorders, inflammatory diseases, cardiovascular diseases, pain and burns in a mammal

PYRIMIDINE DERIVATIVES

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Page/Page column 95, (2011/04/14)

The invention concerns benzamide compounds of Formula (I), or a pharmaceutically acceptable salt thereof, where R1, ring A, n, R3, and R4 are as defined in the description. The present invention also relates to processes for the preparation of such compounds, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use as an antiproliferative agent in the prevention or treatment of tumours or other proliferative conditions which are sensitive to the inhibition of EphB4, and/or EphA2 and/or Src kinases.

Identification of 3-sulfonylindazole derivatives as potent and selective 5-HT6 antagonists

Liu, Kevin G.,Robichaud, Albert J.,Greenfield, Alexander A.,Lo, Jennifer R.,Grosanu, Cristina,Mattes, James F.,Cai, Yanxuan,Zhang, Guo Ming,Zhang, Jean Y.,Kowal, Dianne M.,Smith, Deborah L.,Di, Li,Kerns, Edward H.,Schechter, Lee E.,Comery, Thomas A.

scheme or table, p. 650 - 662 (2011/02/28)

As part of our efforts to develop agents for cognitive enhancement, we have been focused on the 5-HT6 receptor in order to identify potent and selective ligands for this purpose. Herein we report the identification of a novel series of 3-sulfonylindazole derivatives with acyclic amino side chains as potent and selective 5-HT6 antagonists. The synthesis and detailed SAR of this class of compounds are reported.

SUBSTITUTED N-(1H-INDAZOL-4-YL)IMIDAZO[1, 2-A]PYRIDINE-3- CARBOXAMIDE COMPOUNDS AS CFMS INHIBITORS

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Page/Page column 75; 76; 119; 120, (2011/07/09)

Compounds of Formula (I): and pharmaceutically acceptable salts thereof in which R1, R2, R3, R4 and R5 have the meanings given in the specification, are inhibitors of cFMS and are useful in the treatment of bone-related diseases, cancer, autoimmune disorders, inflammatory diseases, cardiovascular diseases and pain.

RAF INHIBITOR COMPOUNDS AND METHODS OF USE THEREOF

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Page/Page column 22, (2010/04/23)

Compounds of Formulas (I), (IIA) and (IIIA) are useful for inhibiting Raf kinase and for treating disorders mediated thereby. Methods of using compounds of Formulas (I), (IIA) and (IIIA) and stereoisomers and pharmaceutically acceptable salts thereof, for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions are disclosed.

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