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4-Tetrazol-1-yl-benzoic acid is a chemical compound that belongs to the class of benzoic acids, characterized by the presence of a tetrazol-1-yl group attached to a benzoic acid structure. 4-TETRAZOL-1-YL-BENZOIC ACID exhibits diverse biological activities, such as antifungal, antibacterial, and antiproliferative properties, making it a promising candidate for applications in pharmaceuticals and agrochemicals. The unique reactivity and functional properties imparted by the tetrazol-1-yl group in its chemical structure also render it a valuable building block for the synthesis of various organic compounds. However, proper handling and use of 4-TETRAZOL-1-YL-BENZOIC ACID are essential to adhere to safety protocols and guidelines due to potential hazards associated with its chemical properties.

78190-05-3

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78190-05-3 Usage

Uses

Used in Pharmaceutical Industry:
4-Tetrazol-1-yl-benzoic acid is used as a pharmaceutical intermediate for the development of drugs with antifungal, antibacterial, and antiproliferative properties. Its unique reactivity and functional properties contribute to the synthesis of various organic compounds with potential therapeutic applications.
Used in Agrochemical Industry:
4-Tetrazol-1-yl-benzoic acid is used as an active ingredient in agrochemicals for its antifungal and antibacterial properties, helping to protect crops from various diseases and pests, thereby improving crop yield and quality.
Used in Organic Synthesis:
4-Tetrazol-1-yl-benzoic acid is used as a valuable building block in organic synthesis, enabling the creation of a wide range of organic compounds with diverse applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Research and Development:
4-Tetrazol-1-yl-benzoic acid is utilized in research and development for exploring its potential applications and properties, as well as for the discovery of new compounds and materials with improved performance and functionality.

Check Digit Verification of cas no

The CAS Registry Mumber 78190-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,1,9 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 78190-05:
(7*7)+(6*8)+(5*1)+(4*9)+(3*0)+(2*0)+(1*5)=143
143 % 10 = 3
So 78190-05-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N4O2/c13-8(14)6-1-3-7(4-2-6)12-5-9-10-11-12/h1-5H,(H,13,14)

78190-05-3 Well-known Company Product Price

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  • Aldrich

  • (CBR01407)  4-(1H-Tetrazol-1-yl)benzoic acid  AldrichCPR

  • 78190-05-3

  • CBR01407-1G

  • 1,930.50CNY

  • Detail

78190-05-3SDS

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 4-(tetrazol-1-yl)benzoic acid

1.2 Other means of identification

Product number -
Other names 4-tetrazolylbenzoic 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:78190-05-3 SDS

78190-05-3Relevant academic research and scientific papers

New compounds, pharmaceutical compositions and uses thereof

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Paragraph 0363; 0364, (2013/03/28)

The present invention relates to compounds of general formula I, wherein the groups R1, LP, LQ, Ar, m and n are as defined in the application, which have valuable pharmacological properties, and in particular bind to the GPR119 receptor and modulate its activity.

N- CYCLOPROPYL - N- PIPERIDINYLBENZAMIDES AS GPR119 MODULATORS

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Page/Page column 87, (2012/10/07)

The present invention relates to compounds of general formula I, wherein the groups R1, LP, LQ, Ar, mand n are as defined in the application, which have valuable pharmacological properties, and in particular bind to the GPR119 receptor and modulate its activity.

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