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19029-32-4

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19029-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19029-32-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,2 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19029-32:
(7*1)+(6*9)+(5*0)+(4*2)+(3*9)+(2*3)+(1*2)=104
104 % 10 = 4
So 19029-32-4 is a valid CAS Registry Number.

19029-32-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,12-dihydrobenzo[b]phenazine

1.2 Other means of identification

Product number -
Other names Benzo[b]phenazine,5,12-dihydro

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19029-32-4 SDS

19029-32-4Downstream Products

19029-32-4Relevant articles and documents

Wavelength selective photoactivated autocatalytic oxidation of 5,12-dihydrobenzo[: B] phenazine and its application in metal-free synthesis

Bian, Lei,Feng, Xiaotong,Guo, Guangsheng,Ma, Jie,Pu, Qiaosheng,Wang, Xiayan,Wang, Yuanhang,Zhao, Lei,Zhao, Lizhi

, p. 9949 - 9954 (2020)

Photochemical stability of 5,12-dihydrobenzo[b]phenazine (DHBP) was investigated with LEDs with central emission wavelengths in a range of 365 to 595 nm. Photochemical conversion of DHBP to benzo[b]phenazine (BP) was observed with wavelengths upto 516 nm. Light of 490 and 516 nm is not absorbed by DHBP, but photoactivated autocatalytic oxidation of DHBP to BP with these wavelengths was confirmed. The reaction rate is in a range of 111-208 μg min-1 with these LEDs. The mechanism of the reaction was examined and the experimental results exclude the intermolecular interaction such as the F?rster resonance energy transfer, the intermolecular charge transfer, the photoinduced electron transfer and the formation of an exciplex. The formation of the reactive oxygen species was verified with electron paramagnetic resonance, which indicates its potential in the synthesis. When sunlight was used as the light source, the oxidation rate of 1 mg mL-1 DHBP was 393 μg min-1. Same autocatalytic oxidation was also observed on similar compounds and it can be used for producing metal-free organic substances for semiconductors.

Triplet Dynamic Nuclear Polarization of Guest Molecules through Induced Fit in a Flexible Metal–Organic Framework**

Fujiwara, Saiya,Kimizuka, Nobuo,Matsumoto, Naoto,Nishimura, Koki,Tateishi, Kenichiro,Uesaka, Tomohiro,Yanai, Nobuhiro

supporting information, (2022/01/19)

Dynamic nuclear polarization utilizing photoexcited triplet electrons (triplet-DNP) has great potential for room-temperature hyperpolarization of nuclear spins. However, the polarization transfer to molecules of interest remains a challenge due to the fast spin relaxation and weak interaction with target molecules at room temperature in conventional host materials. Here, we demonstrate the first example of DNP of guest molecules in a porous material at around room temperature by utilizing the induced-fit-type structural transformation of a crystalline yet flexible metal–organic framework (MOF). In contrast to the usual hosts, 1H spin-lattice relaxation time becomes longer by accommodating a pharmaceutical model target 5-fluorouracil as the flexible MOF changes its structure upon guest accommodation to maximize the host–guest interactions. Combined with triplet-DNP and cross-polarization (CP), this system realizes an enhanced 19F NMR signal of guest target molecules.

LIGHT-EMITTING MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE, ORGANIC ELECTROLUMINESCENT DEVICE USING SAME, AND MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE

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Paragraph 0163-0165, (2016/10/17)

In the present invention, disclosed are a novel aromatic compound with outstanding light-emitting efficiency and heat stability, a manufacturing method thereof and an organic electronic device including the novel aromatic compound. For this, in the present invention, provided are a ring-formed aromatic compound and a novel aromatic amine derivative denoted by chemical formula 1 for improving performance of the device.COPYRIGHT KIPO 2015

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