3931-52-0

Usage

Uses

Used in Pharmaceutical Industry:
1-Benzyl-1-methylhydrazine is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its role in this industry is crucial for creating the building blocks of medications that address a range of health conditions.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 1-Benzyl-1-methylhydrazine serves as an intermediate in the production of agrochemicals. It aids in the synthesis of compounds that are vital for crop protection and enhancement of agricultural yields.
Used in Organic Synthesis:
1-Benzyl-1-methylhydrazine is also utilized as a chemical intermediate in organic synthesis, where it participates in various chemical reactions to form a wide array of organic compounds used in different industries, including but not limited to the production of dyes, polymers, and other specialty chemicals.

InChI:InChI=1/C8H12N2/c1-10(9)7-8-5-3-2-4-6-8/h2-6H,7,9H2,1H3

Upstream product

• 937-40-6 Benzylmethylnitrosamin 
• 103-67-3 benzyl-methyl-amine 
• 100-39-0 benzyl bromide 
• 60-34-4 methylhydrazine 
• 104573-75-3 3-amino-1-benzyl-4,5-dihydro-1-methyl-1H-pyrazolium bromide 

Downstream Products

• 5103-31-1 N-Methyl-N-benzyl-N'-(2,6-dichlorbenzyliden)-hydrazin 
• 29817-13-8 N-Methyl-N-benzyl-N'-isobutyryl-hydrazin 
• 21075-67-2 4-tert.-Butyl-1-benzyl-1-methyl-thiosemicarbazid 
• 97216-15-4 2-Hydroxy-thiobenzoesaeure-(N²-methyl-N²-benzyl-hydrazid) 
• 97663-72-4 2-(Benzyl-methyl-hydrazono)-1,2-diphenyl-ethanone 
• 184294-78-8 (S,S,R)-1-[2-(N-t-butoxycarbonyl)amino-2-benzyl-1-hydroxypropyl]-N-methyl-N-benzylaminobenzoylimide 

Relevant academic research and scientific papers

N-Isocyanodialkylamines generated in situ for the Joullié–Ugi reaction with indolenines

N-Isocyanodialkylamines are rare isocyanide surrogates for the Ugi-type reactions. To avoid problems with instability and the obnoxious smell of these reagents, we optimized and employed a convenient protocol for in situ dehydration of N,N-dialkyl-N′-formyl hydrazines to give the respective N-isocyanodialkylamines which were utilized in the reaction with indolenines and acetic acid. The reaction was demonstrated to give modest to excellent yields of products incorporating the N-isocyanodialkylamine but not the carboxylic acid component.

Cephalosporin derivatives

7 α-formamido cephalosporin derivatives having a 3[N-(optionally substituted)aminothiopyridinium thiomethyl] substituent have anti-bacterial activity and are of use in anti-bacterial therapy. Processes for the preparation thereof and intermediates for use in these processes are also disclosed.

Amidrazones 13. A Convenient Method for the Preparation of 1-Alkyl-1-methylhydrazines

An efficient one-pot procedure for the preparation of 1-alkyl-1-methylhydrazines from methylhydrazine via base-promoted hydrolysis of 1-alkyl-3-amino-4,5-dihydro-1-methyl-1H-pyrazolium halides (3) is described.

AMIDRAZONES 10. STEVENS REARRANGEMENT OF 1-BENZYL AND 1-ALLYL-SUBSTITUTED-3-AMINO-4,5-DIHYDRO-1-PHENYL-1H-PYRAZOLIUM BROMIDES

2-Benzyl-3-imino-1-phenylpyrazolidine (5a) and 2-allyl-3-imino-1-phenylpyrazolidine (5b) are obtained by the base-promoted rearrangement of the title compounds (4a and 4b).