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5-(4-Nitro-pyrazol-1-ylmethyl)-furan-2-carboxylic acid methyl ester is a complex organic compound with the molecular formula C11H10N2O6. It features a furan-2-carboxylic acid core, with a methyl ester group attached to the carboxylic acid, indicating the presence of a methyl ester functional group. The molecule also contains a pyrazole ring, which is substituted with a nitro group at the 4-position and a methylene bridge connecting it to the furan ring. This chemical structure suggests potential applications in pharmaceuticals or as a synthetic intermediate due to its unique arrangement of functional groups.

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  • 402614-78-2 Structure
  • Basic information

    1. Product Name: 5-(4-NITRO-PYRAZOL-1-YLMETHYL)-FURAN-2-CARBOXYLIC ACID METHYL ESTER
    2. Synonyms: 5-(4-NITRO-PYRAZOL-1-YLMETHYL)-FURAN-2-CARBOXYLIC ACID METHYL ESTER;AKOS B001099;METHYL 5-[(4-NITRO-1H-PYRAZOL-1-YL)METHYL]-2-FUROATE;ART-CHEM-BB B001099;TIMTEC-BB SBB009195;5-[(4-nitro-1-pyrazolyl)methyl]-2-furancarboxylic acid methyl ester;BAS 08302046;methyl 5-[(4-nitropyrazol-1-yl)methyl]furan-2-carboxylate
    3. CAS NO:402614-78-2
    4. Molecular Formula: C10H9N3O5
    5. Molecular Weight: 251.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 402614-78-2.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.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-(4-NITRO-PYRAZOL-1-YLMETHYL)-FURAN-2-CARBOXYLIC ACID METHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(4-NITRO-PYRAZOL-1-YLMETHYL)-FURAN-2-CARBOXYLIC ACID METHYL ESTER(402614-78-2)
    11. EPA Substance Registry System: 5-(4-NITRO-PYRAZOL-1-YLMETHYL)-FURAN-2-CARBOXYLIC ACID METHYL ESTER(402614-78-2)
  • 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: 402614-78-2(Hazardous Substances Data)

402614-78-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 402614-78-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,2,6,1 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 402614-78:
(8*4)+(7*0)+(6*2)+(5*6)+(4*1)+(3*4)+(2*7)+(1*8)=112
112 % 10 = 2
So 402614-78-2 is a valid CAS Registry Number.

402614-78-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 5-[(4-nitro-1H-pyrazol-1-yl)methyl]-2-furoate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:402614-78-2 SDS

402614-78-2Relevant articles and documents

AMINOPYRAZOLE DERIVATIVES

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Page/Page column 31, (2011/02/26)

The invention relates to aminopyrazole derivatives of formula (I), wherein A, E, R1 and R2 are as defined in the description, their preparation and their use as pharmaceutically active compounds.

Synthesis, characterization and cardioprotective activity of some novel benzotriazole and pyrazole derivatives

Gudaparthi, Vijayalakshmi,Bharathi,Panda, Jagadeesh

scheme or table, p. 5323 - 5330 (2012/07/28)

A series of N-(1-(1H-benzo[d]) [1,2,3]triazol-1-yl)-2,2-dimethyl propyl)-2-(substituted phenyl) acetamide derivatives and methyl 5-((4- (2,5-disubstituted phenyl) furan-2 carboxylate derivatives are prepared from different substituted aryl carboxylic acids, phenyl acetic acid and cinnamic acid, respectively. All the synthesized compounds are investigated for cardioprotective activity by ischemia reperfusion method, while all the compounds show significant activity.

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