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BENZOFUROXAN-5-CARBOXYLIC ACID, also known as 1,2,5-Oxadiazole 4-oxide 2-furanecarboxylic acid, is a chemical compound belonging to the benzofuroxan family. It has a chemical formula of C5H2N2O5 and a molecular weight of 172.08 g/mol. BENZOFUROXAN-5-CARBOXYLIC ACID is primarily used in chemical research and synthesis due to its unique properties. However, its stability, toxicity, and typical reactions are not well-documented, necessitating careful handling and use by trained professionals. It is advised to store BENZOFUROXAN-5-CARBOXYLIC ACID in a cool, dry environment, away from strong oxidizing agents.

6086-24-4

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6086-24-4 Usage

Uses

Used in Chemical Research:
BENZOFUROXAN-5-CARBOXYLIC ACID is used as a research compound for its unique chemical properties, contributing to the advancement of scientific knowledge in the field of chemistry.
Used in Synthesis:
BENZOFUROXAN-5-CARBOXYLIC ACID is used as a synthetic intermediate in the production of various chemical compounds, facilitating the creation of new materials and substances.

Check Digit Verification of cas no

The CAS Registry Mumber 6086-24-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,8 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6086-24:
(6*6)+(5*0)+(4*8)+(3*6)+(2*2)+(1*4)=94
94 % 10 = 4
So 6086-24-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H24N4O2S3/c21-13(19-7-3-1-4-8-19)11-23-15-17-16(25-18-15)24-12-14(22)20-9-5-2-6-10-20/h1-12H2

6086-24-4 Well-known Company Product Price

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  • Alfa Aesar

  • (L12011)  Benzofuroxan-5-carboxylic acid, 97%   

  • 6086-24-4

  • 1g

  • 750.0CNY

  • Detail
  • Alfa Aesar

  • (L12011)  Benzofuroxan-5-carboxylic acid, 97%   

  • 6086-24-4

  • 5g

  • 2886.0CNY

  • Detail

6086-24-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-oxido-2,1,3-benzoxadiazol-1-ium-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names Benzofuroxan-5-carboxylic acid

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:6086-24-4 SDS

6086-24-4Relevant academic research and scientific papers

Synthesis and biological evaluation of novel histone deacetylases inhibitors with nitric oxide releasing activity

Duan, Wenwen,Hou, Jinning,Chu, Xiaojing,Li, Xiaoqian,Zhang, Jian,Li, Jin,Xu, Wenfang,Zhang, Yingjie

, p. 4481 - 4488 (2015/08/03)

A novel series of histone deacetylases inhibitors (HDACIs) containing benzofuroxan pharmacophore as nitric oxide (NO) donor were designed based on the combination principle and 'multifunctional drugs' theory. As a novel study on embedding NO donor into th

BICYCLIC AMIDES FOR ENHANCING GLUTAMATERGIC SYNAPTIC RESPONSES

-

Paragraph 0088, (2015/11/16)

This invention relates to compounds, pharmaceutical compositions and methods for use in the prevention and treatment of cerebral insufficiency, including enhancement of receptor functioning in synapses in brain networks responsible for basic and higher order behaviors. These brain networks, which are involved in regulation of breathing, and cognitive abilities related to memory impairment, such as is observed in a variety of dementias, in imbalances in neuronal activity between different brain regions, as is suggested in disorders such as Parkinson's disease, schizophrenia, respiratory depression, sleep apneas, attention deficit hyperactivity disorder and affective or mood disorders, and in disorders wherein a deficiency in neurotrophic factors is implicated, as well as in disorders of respiration such as overdose of an alcohol, an opiate, an opioid, a barbiturate, an anesthetic, or a nerve toxin, or where the respiratory depression results form a medical condition such as central sleep apnea, stroke-induced central sleep apnea, obstructive sleep apnea, congenital hypoventilation syndrome, obesity hypoventilation syndrome, sudden infant death syndrome, Rett syndrome, spinal cord injury, traumatic brain injury, Cheney-Stokes respiration, Ondines curse, Prader-Willi's syndrome and drowning, hi a particular aspect, the invention relates to bicyclic amide compounds useful for treatment of such conditions, and methods of using these compounds for such treatment.

Synthesis of carboxyimidamide-substituted benzo[c][1,2,5]oxadiazoles and their analogs, and evaluation of biological activity against Leishmania donovani

Keurulainen, Leena,Heiskari, Mikko,Nenonen, Satu,Nasereddin, Abedelmajeed,Kopelyanskiy, Dmitry,Leino, Teppo O.,Yli-Kauhaluoma, Jari,Jaffe, Charles L.,Kiuru, Paula

, p. 1673 - 1678 (2015/09/15)

A facile synthesis route to carboxyimidamide-substituted benzoxadiazoles and related derivatives was developed. A total of 25 derivatives were synthesized. They were evaluated for antileishmanial activity by inhibition of Leishmania donovani axenic amastigote growth using a fluorescent viability microplate assay. The most promising derivative (14) demonstrated an antileishmanial EC50 of 4.0 μM, and it also showed activity in infected macrophages (EC50 5.92 μM) without signs of cytotoxicity.

Straightforward one-pot synthesis of benzofuroxans from o-halonitrobenzenes in ionic liquids

Sheremetev, Aleksei B.,Aleksandrova, Nataliya S.,Ignat'Ev, Nikolai V.,Schulte, Michael

scheme or table, p. 95 - 97 (2012/07/03)

Treatment of o-halonitrobenzenes with sodium azide in a [empyrr][BF4]/Bu4NBr/H2O system gives benzofuroxans in high yields, with the recovery and reuse of the ionic liquid for at least ten times.

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