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2-Benzofurancarboximidamide, N-hydroxy-, also known as a benzofuran derivative, is a chemical compound with the molecular formula C9H7N3O2. It features an imidamide group substituted with a hydroxy group at the N-position, which contributes to its unique structure and pharmacological properties. 2-Benzofurancarboximidamide,N-hydroxyis recognized for its antitumor and cytotoxic activities, positioning it as a promising candidate for the development of innovative cancer therapies.

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  • 65695-07-0 Structure
  • Basic information

    1. Product Name: 2-Benzofurancarboximidamide,N-hydroxy-
    2. Synonyms: 2-Benzofurancarboximidamide,N-hydroxy-;2-Benzofurancarboximidamide,N-hydroxy-(9CI);2-Benzofurancarboxamide oxime;Brn 0006957;N-Hydroxy-2-benzofurancarboximidamide
    3. CAS NO:65695-07-0
    4. Molecular Formula: C9H8N2O2
    5. Molecular Weight: 176.17202
    6. EINECS: N/A
    7. Product Categories: AMIDINE
    8. Mol File: 65695-07-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 378.1 °C at 760 mmHg
    3. Flash Point: 182.5 °C
    4. Appearance: /
    5. Density: 1.4 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Benzofurancarboximidamide,N-hydroxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Benzofurancarboximidamide,N-hydroxy-(65695-07-0)
    11. EPA Substance Registry System: 2-Benzofurancarboximidamide,N-hydroxy-(65695-07-0)
  • 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: 65695-07-0(Hazardous Substances Data)

65695-07-0 Usage

Uses

Used in Pharmaceutical Industry:
2-Benzofurancarboximidamide, N-hydroxyis used as a potential antitumor agent for its demonstrated cytotoxic effects on cancer cells. Its specific mechanism of action and therapeutic applications are under investigation, but its capacity to target and inhibit tumor growth makes it a valuable subject for further research in medicinal chemistry and drug development.
Used in Cancer Research:
In the field of cancer research, 2-Benzofurancarboximidamide, N-hydroxyis utilized to explore its potential as a new therapeutic agent. Its unique chemical structure and observed antitumor activities are of interest to scientists seeking novel compounds that can effectively combat various types of cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 65695-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,9 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65695-07:
(7*6)+(6*5)+(5*6)+(4*9)+(3*5)+(2*0)+(1*7)=160
160 % 10 = 0
So 65695-07-0 is a valid CAS Registry Number.

65695-07-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Benzofurancarboximidamide,N-hydroxy-

1.2 Other means of identification

Product number -
Other names benzofuryl-2 amidoxime

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:65695-07-0 SDS

65695-07-0Upstream product

65695-07-0Downstream Products

65695-07-0Relevant articles and documents

Chloro-oxime derivatives as novel small molecule chaperone amplifiers

Zhou, Yuefen,Vu, Khang,Chen, Yongsheng,Pham, John,Brady, Thomas,Liu, Gang,Chen, Jinhua,Nam, Joonwoo,Murali Mohan Reddy,Au, Qingyan,Yoon, Il Sang,Tremblay, Marie-Helene,Yip, Gary,Cher, Charmian,Zhang, Bin,Barber, Jack R.,Ng, Shi Chung

scheme or table, p. 3128 - 3135 (2010/01/16)

Chloro-oxime derivatives were investigated as novel small molecule chaperone amplifiers. Lead optimization led to the discovery of compounds that displayed potent HSF1 activation activity, significant cytoprotection in MG-132 stress, ER stress and PolyQ stress cell models (EC50 10 μM).

BENZOFURYL DERIVATIVES AND THEIR USE

-

, (2008/06/13)

The invention is concerned with the use of compounds of general formula (I) wherein R1-R4signify hydrogen, halogen, lower-alkyl, lower-alkoxy, aryl, benzyloxy, lower-alkoxy-lower-alkyl, lower-alkyl-sulphanyl, lower-alkyl-sulphanyl-lower-alkyl or R1and R2t

METHOD OF TREATING DISEASES OF THE CNS

-

, (2008/06/13)

The invention is concerned with the use of compounds of the general formula STR1 wherein R 1-R 4 signify hydrogen, halogen, lower-alkyl, lower-alkoxy, aryl, benzyloxy, lower-alkoxy-lower-alkyl, lower-alkyl-sulphanyl, lower-alkyl-sulphanyl-lower-alkyl or R

Analgesic and antiinflammatory properties of 2-benzofuran amidoximes

Riffaud,Dupont,Rene,Royer

, p. 577 - 581 (2007/10/02)

2-Benzofuran carboximidamide and various of its substituted derivatives have been tested for analgesic, anti-inflammatory and ulcerigeneous activity. For comparison, the same tests were performed with 2-naphto[2,1-b]furan carboximidamide, some 3-benzopyrancarboximidamides and 2-furan carboximidamide. Most 2-benzofurancarboximidamides show to have interesting analgesic properties. Some of them are also anti-inflammatories. 3-Methyl-5-bromo-2-benzofurancarboximidamide can be compared to aspirin and phenylbutazone as analgesic and anti-inflammatory respectively; no significant ulcerigeneous effect was noted for this compound.

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