What is the (3,4-Diaminophenyl)phenylmethanone?

(3,4-Diaminophenyl)phenylmethanone is yellow to ochre-yellow powder, while it's Molecular Formula is C13H12N2O. yellow to ochre-yellow powder 3,4-Diaminobenzophenone is used in the synthesis of 2-Amino-5(6)-benzoylbenzimidazole (A593760), which is a minor urinary metabolite of Mebendazole (M200500) in man. Mebendazole impurity.

What is the CAS number for (3,4-Diaminophenyl)phenylmethanone?

The CAS number of (3,4-Diaminophenyl)phenylmethanone is 39070-63-8.

What is (3,4-Diaminophenyl)phenylmethanone (39070-63-8) used for?

(3,4-Diaminophenyl)phenylmethanone is an organic compound with the molecular formula C13H11N2O. It is a derivative of phenylmethanone, featuring a phenyl ring attached to a methanone group, with two amino groups attached to the 3rd and 4th positions of the phenyl ring. (3,4-Diaminophenyl)phenylmethanone is known for its potential applications in various industries due to its unique chemical structure and properties.InChI:InChI=1/C13H12N2O/c14-11-7-6-10(8-12(11)15)13(16)9-4-2-1-3-5-9/h1-8H,14-15H2

What is the (3,4-Diaminophenyl)phenylmethanone?

(3,4-Diaminophenyl)phenylmethanone is yellow to ochre-yellow powder, while it's Molecular Formula is C13H12N2O. yellow to ochre-yellow powder 3,4-Diaminobenzophenone is used in the synthesis of 2-Amino-5(6)-benzoylbenzimidazole (A593760), which is a minor urinary metabolite of Mebendazole (M200500) in man. Mebendazole impurity.

What is the CAS number for (3,4-Diaminophenyl)phenylmethanone?

The CAS number of (3,4-Diaminophenyl)phenylmethanone is 39070-63-8.

What is (3,4-Diaminophenyl)phenylmethanone (39070-63-8) used for?

(3,4-Diaminophenyl)phenylmethanone is an organic compound with the molecular formula C13H11N2O. It is a derivative of phenylmethanone, featuring a phenyl ring attached to a methanone group, with two amino groups attached to the 3rd and 4th positions of the phenyl ring. (3,4-Diaminophenyl)phenylmethanone is known for its potential applications in various industries due to its unique chemical structure and properties.InChI:InChI=1/C13H12N2O/c14-11-7-6-10(8-12(11)15)13(16)9-4-2-1-3-5-9/h1-8H,14-15H2

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(3,4-Diaminophenyl)phenylmethanone

CAS No.: 39070-63-8
Purity: 99%

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Offer Chemical Raw Material (3,4-Diaminophenyl)phenylmethanone 39070-63-8 In Stock

Molecular Formula: C13H12N2O
Molecular Weight: 212.251
Appearance/Colour: yellow to ochre-yellow powder
Vapor Pressure: 5.76E-08mmHg at 25°C
Melting Point: 115-117 °C(lit.)
Refractive Index: 1.673
Boiling Point: 440.7 °C at 760 mmHg
PKA: 2.96±0.10(Predicted)
Flash Point: 220.3 °C
PSA： 69.11000
Density: 1.233 g/cm³
LogP: 3.24440

(3,4-Diaminophenyl)phenylmethanone(Cas 39070-63-8) Usage

Purification Methods

Crystallise it from *C6H6/pet ether and sublime it in vacuo [Ayyanger et al. Org Prep Proced Int 23 627 1991].

InChI:InChI=1/C13H12N2O/c14-11-7-6-10(8-12(11)15)13(16)9-4-2-1-3-5-9/h1-8H,14-15H2

39070-63-8 Relevant articles

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Synthesis and antiparasitic activity of Albendazole and Mebendazole analogues

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Albendazole (Abz) and Mebendazole (Mbz) ...

39070-63-8 Process route

: 33609-48-2
3,4-dinitrobenzophenone

: 39070-63-8
4-benzoylbenzene-1,2-diamine

Conditions

Conditions	Yield
With hydrogen; nickel; In tetrahydrofuran; at 30 - 40 ℃;
With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 24h;

: 528-45-0
3,4-dinitrobenzoic acid

: 39070-63-8
4-benzoylbenzene-1,2-diamine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 1.) SOCl₂, 2.) AlCl₃ / 1.) reflux, 10 min, 2.) room temp., 24 h, then 40-50 deg C, 0.5 h 2: H₂ / Raney nickel / tetrahydrofuran / 30 - 40 °C With aluminium trichloride; thionyl chloride; hydrogen; nickel; In tetrahydrofuran;
Multi-step reaction with 3 steps 1: thionyl chloride / N,N-dimethyl-formamide / 0 °C 2: aluminum (III) chloride / dichloromethane / 3 h / Reflux; Inert atmosphere 3: palladium 10% on activated carbon; hydrogen / methanol / 24 h / 20 °C With aluminum (III) chloride; thionyl chloride; palladium 10% on activated carbon; hydrogen; In methanol; dichloromethane; N,N-dimethyl-formamide; 2: \|Friedel-Crafts Acylation;

Yield

Multi-step reaction with 2 steps

1: 1.) SOCl₂, 2.) AlCl₃ / 1.) reflux, 10 min, 2.) room temp., 24 h, then 40-50 deg C, 0.5 h

2: H₂ / Raney nickel / tetrahydrofuran / 30 - 40 °C

With aluminium trichloride; thionyl chloride; hydrogen; nickel; In tetrahydrofuran;

Multi-step reaction with 3 steps

1: thionyl chloride / N,N-dimethyl-formamide / 0 °C

2: aluminum (III) chloride / dichloromethane / 3 h / Reflux; Inert atmosphere

3: palladium 10% on activated carbon; hydrogen / methanol / 24 h / 20 °C

With aluminum (III) chloride; thionyl chloride; palladium 10% on activated carbon; hydrogen; In methanol; dichloromethane; N,N-dimethyl-formamide; 2: |Friedel-Crafts Acylation;