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CHEMBRDG-BB 4012168, a chemical compound with the molecular formula C11H14N2O, belongs to the benzoylamine class of compounds. It is a white crystalline solid that is soluble in organic solvents such as ether and chloroform. CHEMBRDG-BB 4012168 is commonly used in organic synthesis and pharmaceutical research, and has potential applications in the development of new drugs. CHEMBRDG-BB 4012168 has been studied for its antimicrobial and antifungal properties, and its precise uses and functions in biological systems are still being explored, making it an interesting target for further research and development.

874908-43-7

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874908-43-7 Usage

Uses

Used in Pharmaceutical Research:
CHEMBRDG-BB 4012168 is used as a chemical intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable building block for the development of new drugs.
Used in Organic Synthesis:
CHEMBRDG-BB 4012168 is used as a reagent in various organic synthesis processes. Its versatility allows it to be used in the preparation of a wide range of organic compounds.
Used in Antimicrobial Applications:
CHEMBRDG-BB 4012168 is used as an antimicrobial agent for its potential to inhibit the growth of certain types of bacteria. Its effectiveness in this area is still being studied, and further research is needed to fully understand its capabilities.
Used in Antifungal Applications:
CHEMBRDG-BB 4012168 is used as an antifungal agent for its potential to inhibit the growth of certain types of fungi. Its effectiveness in this area is also being studied, and more research is needed to determine its full potential.
Used in Drug Development:
CHEMBRDG-BB 4012168 is used as a potential candidate for the development of new drugs. Its unique properties and potential applications make it an interesting target for further research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 874908-43-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,9,0 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 874908-43:
(8*8)+(7*7)+(6*4)+(5*9)+(4*0)+(3*8)+(2*4)+(1*3)=217
217 % 10 = 7
So 874908-43-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N2O/c13-7-9-6-11-12-10(9)8-4-2-1-3-5-8/h6-8H,1-5H2,(H,11,12)

874908-43-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-cyclohexyl-1H-pyrazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-cyclohexyl-1H-pyrazole-4-carbaldehyde

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:874908-43-7 SDS

874908-43-7Relevant academic research and scientific papers

Vilsmeier formylation of hydrazones and semicarbazones derived from alkyl, benzyl, and cycloalkyl methyl ketones

Lebedev,Lebedeva,Sheludyakov,Kovaleva,Ustinova,Kozhevnikov

, p. 412 - 416 (2007/10/03)

Formylation of ten accessible phenylhydrazones and semicarbazones derived from alkyl, benzyl, and cycloalkyl methyl ketones with the complex of POCl 3 with dimethylformamide was studied. Depending on the electronic and steric structure of the substrates, the reaction yields 1-phenyl- or 1-unsubstituted 3,4-dialkyl-, 3-alkyl-4-aryl-, or 3-alkyl-4-formylpyrazoles. These compounds can be readily oxidized into the corresponding carboxylic acids. 2005 Pleiades Publishing, Inc.

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