19102-24-0

Basic information

• Product Name: 1-methyl-N-phenylhydrazinecarboxamide
• CAS NO: 19102-24-0
• Molecular Formula: C₈H₁₁N₃O
• Molecular Weight: 165.1924
• Mol File: 19102-24-0.mol
• Article Data: 4

Chemical Properties

• Density: 1.237g/cm³
• Refractive Index: 1.635
• CAS DataBase Reference: 1-methyl-N-phenylhydrazinecarboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-N-phenylhydrazinecarboxamide(19102-24-0)
• EPA Substance Registry System: 1-methyl-N-phenylhydrazinecarboxamide(19102-24-0)

Safety Data

• Hazardous Substances Data: 19102-24-0(Hazardous Substances Data)

Usage

Hydrazine derivative

A derivative of hydrazine (N2H4) This indicates that the compound is structurally related to hydrazine, with modifications in its molecular structure.

Used as an intermediate

In the synthesis of pharmaceuticals and agrochemicals The compound serves as a starting material or building block in the production of various drugs and chemicals used in agriculture.

Solid crystalline substance

The compound's physical form is a solid with a crystalline structure, which means it has a well-ordered and repeating pattern of molecules.

Slightly soluble in water

The compound does not dissolve easily in water, which can affect its solubility, reactivity, and applications.

Potential toxicity

The compound may be harmful if ingested or inhaled This highlights the need for proper handling and safety precautions when working with the substance.

Applications in organic chemistry and chemical synthesis

The compound has potential uses in the synthesis of other organic compounds and chemical reactions, making it a valuable research and industrial tool.

Upstream product

• 60-29-7 diethyl ether 
• 103-71-9 phenyl isocyanate 
• 60-34-4 methylhydrazine 
• 93-97-0 benzoic acid anhydride 
• 86298-24-0 N-phenyl-1H-benzo[d][1,2,3]triazole-1-carboxamide 
• 65-85-0 benzoic acid 

Downstream Products

• 77919-29-0 1-Benzoyl-2-methyl-4-phenylsemicarbazid 
• 1353871-81-4 6-(2-hydroxy-4-oxobicyclo[3.2.1]octa-2-enylcarbonyl)-2-methyl-4-phenyl-1,2,4-triazine-3,5(2H,4H)-dione 
• 1353872-42-0 4-phenyl-2-methyl-1,2,4-triazine-3,5-dione-6-carboxylic acid 
• 1353873-55-8 2-methyl-3,5-dioxo-4-phenyl-2,3,4,5-tetrahydro-1,2,4-triazine-6-carbonyl chloride 
• 1353870-28-6 6-(2-hydroxy-6-oxocyclohexa-1-enecarbonyl)-2-methyl-4-phenyl-1,2,4-triazine-3,5(2H,4H)-dione 
• 1353871-79-0 6-(5-hydroxy-1-methyl-1H-pyrazole-4-carbonyl)-2-methyl-4-phenyl-1,2,4-triazine-3,5(2H,4H)-dione 
• 1353871-90-5 2-methyl-3,5-dioxo-4-phenyl-2,3,4,5-tetrahydro-1,2,4-triazine-6-carboxylic acid, ethyl ester 
• 77919-23-4 4-Methyl-2-phenylamino-5-phenylimino-Δ²-1,3,4-oxadiazolin-hydrochlorid 
• 28538-67-2 1-Methyl-4-phenyl-1,2,4-triazolidin-3,5-dion 
• 3558-91-6 benzo[e][1,3]oxazine-2,4-dione 2-(2-methyl-4-phenyl-semicarbazone) 
• 25976-83-4 2,5-dimethyl-4-phenyl-2,4-dihydro-[1,2,4]triazole-3-thione 

Relevant articles and documents

One-pot preparation of carbamoyl benzotriazoles and their applications in the preparation of ureas, hydrazinecarboxamides and carbamic esters

Carbamoyl benzotriazoles were conveniently synthesized in one-pot from carboxylic acids, diphenyl phosphorazidate (DPPA) and 1H-benzotriazole (BtH). The reactivity and applications of carbamoyl benzotriazoles were also explored. Carbamoyl benzotriazoles react smoothly with amino acids, hydrazines and alcohols, thus providing facile access to the corresponding ureas, hydrazinecarboxamides and carbamic esters, respectively, in good to excellent yields.

Carbazoyl derivatives

A carbazoyl derivative of the general formula: (wherein, R1brepresents a bond, alkylene group of from 1 to 6 carbon atom(s) or alkenylene group of from 2 to 6 carbon atoms,R2brepresents a carbocyclic or heterocyclic ring unsubstituted or substituted by from one to three halogen atom(s), hydroxy group, nitro group, amino group, alkyl or alkoxy group of from 1 to 4 carbon atom(s), 3-aminoureido group, phenoxy group or acylamino group of from 2 to 5 carbon atoms, or R1btogether with R2b, represents an alkyl group of from 1 to 12 carbon atom(s) unsubstituted or substituted by 3-aminoureido group,R3brepresents (1) a hydrogen atom,(2) an alkyl group of from 1 to 6 carbon atom(s) or, (3) a phenyl or benzyl group unsubstituted or substituted by from one to three halogen atom, alkyl or alkoxy group of from 1 to 4 carbon atom(s), hydroxy group or nitro group,Xbrepresents a bond or imino gorup,with the proviso that the compounds wherein the groups shown by Xb-R1b-R2brepresent a phenyl group, 4-aminophenyl gorup, anilino group and 2-thienyl group and the groups shown by R3brepresent a hydrogen atom, are excluded.),or an acid addition salt thereof possesses inhibitory activity on Maillard reaction, and therfore is useful for treating and/or prevention of several diabetic complications and deseases induced by aging.