73907-95-6

Basic information

• Product Name: 6-AMINO-1H-INDAZOLE-7-CARBOXYLIC ACID
• Synonyms: 6-AMINO-1H-INDAZOLE-7-CARBOXYLIC ACID;TIMTEC-BB SBB002550;7-Carboxy-1H-indazole-6-amine;1H-Indazole-7-carboxylic acid, 6-aMino-;6-Amino-7-carboxy-1H-indazole
• CAS NO: 73907-95-6
• Molecular Formula: C₈H₇N₃O₂
• Molecular Weight: 177.16
• Product Categories: Indazoles
• Mol File: 73907-95-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 177 °C (decomp)
• Boiling Point: 501.6±35.0 °C(Predicted)
• Appearance: /
• Density: 1.611
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 16.17±0.40(Predicted)
• CAS DataBase Reference: 6-AMINO-1H-INDAZOLE-7-CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 6-AMINO-1H-INDAZOLE-7-CARBOXYLIC ACID(73907-95-6)
• EPA Substance Registry System: 6-AMINO-1H-INDAZOLE-7-CARBOXYLIC ACID(73907-95-6)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 22
• Hazardous Substances Data: 73907-95-6(Hazardous Substances Data)

Usage

General Description

6-Amino-1H-indazole-7-carboxylic acid is a chemical compound from the indazole class, renowned for its pharmaceutical usefulness. The specific structure and arrangement of atoms in this compound offer it the potential to participate in the creation of several beneficial drugs. During these processes, it is often utilized as a critical intermediate. Its molecular formula is C8H7N3O2 and it is available in the form of a white to off-white powder. The compound is sparingly soluble in water, indicating its likely stability in many physical and chemical conditions. Performing additional research, following safety protocols, and conducting extensive testing is important when using this compound in laboratories or industrial environments.

Upstream product

• 73907-93-4 2-[(E)-Hydroxyimino]-N-(1H-indazol-6-yl)-acetamide 
• 73907-93-4 6-(isonitrosoacetamido)indazole 
• 6967-12-0 6-amino-1H-indazole 
• 77929-34-1 6-(hydroximinoacetyl)-amino-1H-indazole hydrochloride 
• 73907-94-5 pyrrolo<2,3-g>indazole-7,8-dione 

Downstream Products

• 73907-90-1 prox-benzoisoallopurinol 
• 154597-37-2 6-amino-7-indazolecarboxaldehyde 
• 73907-96-7 6-(β-benzoylthioureido)indazole-7-carboxylic acid 
• 73907-99-0 ethyl 6-aminoindazole-7-carboxylate 
• 73907-98-9 6-amino-1H-indazole-7-carboxylic acid methyl ester 
• 75844-39-2 6-amino-7-methoxycarbonyl-1-methylindazol 

Relevant articles and documents

PESTICIDES CONTAINING A BICYCLIC BISAMIDE STRUCTURE

Compounds of formula (I), wherein the substituents are as defined in claim 1, and the agrochemically acceptable salts and all stereoisomers and tautomeric forms of the compounds of formula I can be used as agrochemical active ingredients and can be prepared in a manner known per se.

Benzologs of allopurinol: synthesis of pyrazolo[4,3-g] and [3,4-f]quinazolinones

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Quinazoline derivatives

Novel quinazoline derivatives of the formula (1) STR1 wherein ring C is a pyrazole ring fused to ring B in two vicinal positions thereof that are not fused with ring A. The novel formula (1) compounds or pyrazolo-quinazoline-ones are structurally related to allopurinol, a well known drug useful in the treatment of gout and are expected to replace or complement allopurinol in the therapeutic use thereof. The generic name Benzoallopurinol is suggested for the novel formula (1) compounds; formula (1) includes angular and linear structures of the interfused rings A, B and C. Two methods for producing the novel formula (1) compounds are disclosed. The first method starts from the indazole structure that includes the interfused rings B and C, and ring A is formed on the indazole moiety. The second method starts from the quinazoline structure that includes interfused rings A and B, and the pyrazole ring C is formed on the benzo moiety (ring B) of the quinazoline structure. Either method may lead to angular or linear benzoallopurinols depending upon the substituents introduced into the starting structure for forming the complemental ring thereon.