615-00-9

Usage

Uses

Used in Chemical Synthesis:
(2,4-dimethylphenyl)hydrazine is used as a reagent in organic synthesis for the production of various chemical compounds. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2,4-dimethylphenyl)hydrazine serves as a building block for the synthesis of various pharmaceutical compounds. Its ability to form different chemical entities makes it a crucial component in the development of new drugs and medications.
Used in Dye Production:
(2,4-dimethylphenyl)hydrazine is also utilized in the production of azo dyes, which are a class of organic compounds known for their vibrant colors and wide range of applications in various industries, including textiles, plastics, and printing inks.
Safety Precautions:
Due to its toxic and potentially carcinogenic properties, it is essential to handle (2,4-dimethylphenyl)hydrazine with care. It should be used in a well-ventilated area and appropriate personal protective equipment should be worn to minimize exposure and ensure safety during its use.

InChI:InChI=1/C8H12N2/c1-6-3-4-8(10-9)7(2)5-6/h3-5,10H,9H2,1-2H3

Upstream product

• 95-68-1 2,4-Xylidine 
• 7647-01-0 hydrogenchloride 
• 53559-94-7 2,4-dimethyl-benzenediazonium; chloride 
• 60480-83-3 (2,4-dimethylphenyl)hydrazine hydrochloride 

Downstream Products

• 352522-93-1 1-(2,4-dimethyl-phenyl)-3,4-dimethyl-1H-pyrano[2,3-c]pyrazol-6-one 
• 7456-74-8 di(2,4-dimethylphenyl)carbazone 

Relevant academic research and scientific papers

3-[1-(3-Haloalkyl)triazolyl]phenyl sulphide derivatives as acaricides and insecticides

The present invention constitutes new 3-[1-(3-haloalkyl)triazolyl]phenyl sulphide derivatives of the formula (I) in which A1, A2, B0, B1, B2, B3, R1, R2 and n are as d

Novel chromogenic substances and use thereof for the determination of carboxypeptidase activities

The invention relates to chromogenic compounds and the use thereof for the determination of enzymes of the family of carboxypeptidases N and carboxypeptidases U. The above is more specifically a compound of formula (I) in which A=(1), (2), (3), (4) or (5). R1. R2=H. —CH3, —CH(CH3)2, —OCH3, —Cl.—CF3,—OCF3,—SCH3, R3=an amino acid group which may be hydrolysed by a carboxypeptidase A and R4=a basic amino acid group.

PYRAZOLOPYRIMIDINES AS ANTI - HEPATITS C AGENTS

Pyrazolopyrimidine derivatives of formula (I), or a pharmaceutically acceptable salt thereof, are found to be active against hepatitis C infection, wherein: R1 is C6-C10 aryl, 5- to 10- membered heteroary1, -(C1-C4 alkyl)-(C6-C10 aryl) or -(C1-C4 alkyl)-(5- to 10- membered heteroaryl); R2 is a C6-C10 aryl, C3-C6 carbocyclyl, 5- to 10- membered heteroaryl or 5- to 10- membered heterocyclyl moiety, said moiety being optionally fused to a C6-C10 aryl, C3-C6 carbocyclyl, 5- to 10- membered heteroaryl or 5- to 10-membered heterocyclic ring; and X is -NR'-, -NR'-CO-NR''-, -NR'-L, or -NR'-CO-L-, wherein R' and R'' are the same or different and each represent hydrogen or a C1-C6 alkyl group and L represents a C1-C6 alkylene group, the aryl, heteroaryl, heterocyclyl. and carbocyclyl moieties in the R1 and R2 substituents being unsubstituted or substituted by 1, 2 or 3 substituents selected from halogen, C1-C4 alkyl C1-C4alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, cyano, nitro, C6-C10 aryl, C3-C6 carbocyclyl, 5- to 10- membered heterocyclyl, 5- to 10- membered heteroaryl, -NR'-CO2-R'', -CO2R'', -COR'''-NR'-CO-R''',-CONR'R'',SO2NR'R'',SO2R'''and -O-(CH2)n-R''' substituents, wherein n is from 0 to 4, each R’is the same or different and is hydrogen or C1-C6 alkyl, each R'' is the same or different and is hydrogen, C1-C6 alkyl, C6-C10 aryl, 5- to 10- membered heterocyclyl or 5- to 10- membered heteroaryl, each R''' is the same or different and is C1-C6 alkyl, C6-C10 aryl, 5- to 10- membered heterocyclyl or 5- to 10- membered heteroaryl, and each R'''' is the same or different and is C6-C10 aryl, 5- to 10- membered heterocyclyl or 5- to 10- membered heterocryl, the aryl, heteroaryl, heterocyclyl and carbocyclyl moieties in said substituents being unsubstituted or substituted by a further substituent selected from C1-C4 alkyl, C1-C4 hydroxyalkyl and C1-C4 haloalkyl groups.