CasNo.83992-95-4,4-Bis(4-methylphenyl)aminobenzaldehyde-1,1-diphenyl-hydrazone,4-Bis(4-methylphenyl)aminobenzaldehyde-1,1-diphenyl-hydrazone(83992-95-4) Suppliers

10 Gram	Negotiable

Min.Order :10 Gram
Purity: 98%

Keywords

4,4'-Bis(4-methylphenyl)aminobenzaldehyde-1,1-diphenylhydrazone 4-[Bis(4-methylphenyl)amino]-benzaldehyde diphenylhydrazone 4-Bis(4-methylphenyl)aminobenzaldehyde-1,1-diphenyl-hydrazone 98%

Quick Details

Appearance:Light yellow crystal powder
Application:OLED intermediates
PackAge:25kg/drum; Can be packaged in accordance with customer requirements
ProductionCapacity:|Metric Ton|Day
Storage:Store in a cool, dry place. Store in a tightly closed container
Transportation:By air or By sea or By express

Details:

1.Introduction of 83992-95-4

4-Bis(4-methylphenyl)aminobenzaldehyde-1,1-diphenyl-hydrazone has CAS registry number of 83992-95-4. It is a kind of light yellow crystal powder with purity of 98.0% in our factory packed in 25 kg drum. With its systematic name of 4-(diphenylcarbonohydrazonoyl)-N,N-bis(4-methylphenyl)aniline, it is used as electronic, pharmacetical, electronic chemicals, phenylamine series.

2.Properties of 83992-95-4

ACD/LogP: 10.07
# of Rule of 5 Violations: 1
ACD/LogD (pH 5.5): 10.07
ACD/LogD (pH 7.4): 10.07
ACD/BCF (pH 5.5): 1000000.00
ACD/BCF (pH 7.4): 1000000.00
ACD/KOC (pH 5.5): 7160869.00
ACD/KOC (pH 7.4): 7161482.00
#H bond acceptors: 3
#H bond donors: 0
#Freely Rotating Bonds: 7
Polar Surface Area: 18.84 ²
Index of Refraction: 1.6
Molar Refractivity: 152.488 cm³
Molar Volume: 445.191 cm³
Polarizability: 60.451 10-24cm³
Surface Tension: 41.1389999389648 dyne/cm
Density: 1.05 g/cm³Flash Point: 335.568 °C
Enthalpy of Vaporization: 93.353 kJ/mol
Boiling Point: 631.25 °C at 760 mmHg
Vapour Pressure: 0 mmHg at 25°C

3.Structure Descriptors of 83992-95-4

(1)InChI: InChI=1S/C33H29N3/c1-26-13-19-29(20-14-26)35(30-21-15-27(2)16-22-30)31-23-17-28(18-24-31)25-34-36(32-9-5-3-6-10-32)33-11-7-4-8-12-33/h3-25H,1-2H3
(2)InChIKey: WCVWLLLVYFDRTB-UHFFFAOYSA-N
(3)Canonical SMILES : CC1=CC=C(C=C1)N(C2=CC=C(C=C2)C)C3=CC=C(C=C3)C=NN(C4=CC=CC=C4)C5=CC=CC=C5