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4-bromo-N-(4-bromobenzoyl)benzohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 69673-99-0 Structure
  • Basic information

    1. Product Name: 4-bromo-N-(4-bromobenzoyl)benzohydrazide
    2. Synonyms:
    3. CAS NO:69673-99-0
    4. Molecular Formula: C14H10Br2N2O2
    5. Molecular Weight: 398.054
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69673-99-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 587.5°Cat760mmHg
    3. Flash Point: 309.1°C
    4. Appearance: N/A
    5. Density: 1.727g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-bromo-N-(4-bromobenzoyl)benzohydrazide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-bromo-N-(4-bromobenzoyl)benzohydrazide(69673-99-0)
    11. EPA Substance Registry System: 4-bromo-N-(4-bromobenzoyl)benzohydrazide(69673-99-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 69673-99-0(Hazardous Substances Data)

69673-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69673-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,7 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69673-99:
(7*6)+(6*9)+(5*6)+(4*7)+(3*3)+(2*9)+(1*9)=190
190 % 10 = 0
So 69673-99-0 is a valid CAS Registry Number.

69673-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-bis(4-aminophenyl)urea

1.2 Other means of identification

Product number -
Other names N,N'-Bis-(4-brom-benzoyl)-hydrazin

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:69673-99-0 SDS

69673-99-0Relevant articles and documents

Highly potent, broadly active antifungal agents for the treatment of invasive fungal infections

Baugh, Simon D.P.,Chaly, Anna,Weaver, Damian G.,Pelletier, Jeffrey C.,Thanna, Sandeep,Freeman, Katie B.,Reitz, Allen B.,Scott, Richard W.

, (2021)

Invasive fungal infections have become an important healthcare issue due in large part to high mortality rates under standard of care (SOC) therapies creating an urgent need for new and effective anti-fungal agents. We have developed a series of non-pepti

NOVEL HETEROAROMATIC COMPOUNDS EXHIBITING ANTIFUNGAL ACTIVITY AND THEIR METHOD OF USE

-

Paragraph 0495, (2021/12/28)

Pharmaceutical compositions of the invention comprise herteroaromatic compounds having a disease-modifying action in the treatment of fungal infections and diseases associated with fungal infection.

Compounds comprising benzophenone group, Organic electronic device comprising organic layers comprising the photo-cured of the monomer compounds

-

Paragraph 0377-0381, (2021/03/09)

The compound represented by Formula I or II is provided as an organic material layer material of an organic electronic device. The benzophenone functional group-containing compound represented by the following Chemical I or Chemical Formula II: I (Chemical Formula Ar -) (R). 1 -R2 -Bpm In the formula, m is 1 and 10, and Ar is a substituted or unsubstituted m having a C-order linking group. 6 -C60 Substituted or unsubstituted m having aryl group, C nd-linking group3 -C60 Substituted or unsubstituted fused m with heteroaryl groups or C primary linking groups6 -C60 Aryl group, R1 And R2 Each independently represents a simple bond, O - a substituted or unsubstituted C. 6 -C30 Arylene group, substituted or unsubstituted C3 -C30 Heteroarylene group, substituted or unsubstituted C1 -C10 The alkylene group and Bp are 1 divalent linking groups derived from benzophenone functional groups. Chemical Formula II. In the formula, n is at least 1 and Ar ' is a substituted or unsubstituted m having a C-order linking group. 6 -C60 Aryl group Substituted or unsubstituted m having a C nd order linker3 -C60 Substituted or unsubstituted fused m with heteroaryl groups or C primary linking groups6 -C60 Aryl group, R3 And R4 Each independently represents a simple bond, O - a substituted or unsubstituted C. 6 -C30 Arylene group, substituted or unsubstituted C3 -C30 Heteroarylene group, substituted or unsubstituted C6 -C30 Fused arylene groups, substituted or unsubstituted C1 -C10 The alkylene group and Bp ' are 1 divalent linking groups derived from benzophenone functional groups.

Oxadiazole- and indolocarbazole-based bipolar materials for green and yellow phosphorescent organic light emitting diodes

Wu, Qiong,Braveenth, Ramanaskanda,Bae, Il-Ji,Zhang, Heng-Qiang,Jung, Hasu,Kim, Miyoung,Chai, Kyu Yun

, (2019/12/11)

New bipolar materials, namely 2-phenyl-5-(4-(5-phenylindolo [3,2-a]carbazol-12(5H)-yl)phenyl)-1,3,4-oxadiazole (ICz-OXD) and 2,5-bis(4-(5-phenylindolo [3,2-a]carbazol-12(5H)-yl)phenyl)-1,3,4-oxadiazole (2ICz-OXD), were designed and synthesized. Tree different devices were fabricated using ICz-OXD and 2ICz-OXD as host and fluorescent materials: a green phosphorescent, yellow phosphorescent, and non-doped fluorescent OLED emitter. The yellow phosphorescent OLED device based on the 2ICz-OXD host presented good maximum current, power, and external quantum efficiencies, whose values were 47.55 cd/A, 49.80 lm/W, and 21.54%, respectively. Its efficiencies were better than those of the devices based on ICz-OXD and on the reference material 4,4′-Bis(N-carbazolyl)-1,1′-biphenyl (CBP). The green phosphorescent OLED device with ICz-OXD revealed higher efficiencies than the device based on 2ICz-OXD. The current, power, and external quantum efficiencies based on ICz-OXD were 49.79 cd/A, 52.14 lm/W, and 16.50%, respectively. The non-doped fluorescent devices that used our bipolar materials (ICz-OXD, 2ICz-OXD) exhibited blue emission at 435 and 442 nm.

Fluorescent probes and application thereof to detection of neurotoxic agents

-

Paragraph 0038-0041, (2020/05/01)

The invention relates to fluorescent probes represented by a general formula I or II which is described in the specification, and application of the fluorescent probes in detection of neurotoxic agents. The fluorescent probes can be used for efficiently d

Compounds comprising benzophenone group, Organic electronic device comprising organic layers comprising the photo-cured of the monomer compounds

-

Paragraph 0382-0386, (2020/08/12)

The present invention provides a compound containing a benzophenone functional group represented by chemical formula I: Ar-(R_1-R_2-Bp)_m or chemical formula II as a material for an organic material layer of an organic electronic device, wherein the compound is the compound containing the benzophenone functional group.COPYRIGHT KIPO 2020

Polyamine monomer of polyimide containing triazole structure and polymer and preparation method of polyamine monomer as well as application

-

Paragraph 0062-0065, (2019/08/06)

The invention discloses a polyamine monomer of polyimide containing a triazole structure and a polymer and a preparation method of the polyamine monomer as well as application, and belongs to the fields of hyperbranched polyimide preparation technology an

Diamine monomer of polyimide containing triazole structure and polymer, preparation method and application thereof

-

Paragraph 0043; 0045; 0046, (2019/07/16)

The invention discloses a polyimide monomer with a triazole structure and a polymer,preparation method and application thereof, and belongs to the fields of polyimide preparation technology and information storage materials. The method comprises the follo

Rapid and Atom Economic Synthesis of Isoquinolines and Isoquinolinones by C–H/N–N Activation Using a Homogeneous Recyclable Ruthenium Catalyst in PEG Media

Deshmukh, Dewal S.,Gangwar, Neha,Bhanage, Bhalchandra M.

, p. 2919 - 2927 (2019/05/10)

Herein, we report an atom-efficient, rapid, green, and sustainable approach to synthesize isoquinolines and isoquinolinones using a homogeneous recyclable ruthenium catalyst in PEG Media assisted by microwave energy. Dibenzoylhydrazine was used for C–H/N–N activation reactions for the first time in combination with ketazine as oxidizing directing groups for annulation reactions with internal alkynes. The developed protocol is environmentally benign due to significantly shortened times with an easy extraction method, higher atom economy, external oxidant and silver or antimony salt free conditions, applicability to a gram scale synthesis, use of biodegradable solvent and wide substrate scope with higher product yields. Moreover, it is worth noting that the established methodology allowed reuse of the catalytic system for up to five successive runs with minimal loss in activity.

Triphenylamine based conjugated microporous polymers for selective photoreduction of CO2 to CO under visible light

Dai, Chunhui,Zhong, Lixiang,Gong, Xuezhong,Zeng, Lei,Xue, Can,Li, Shuzhou,Liu, Bin

supporting information, p. 6606 - 6610 (2019/12/26)

Organic π-conjugated polymers (CPs) have been intensively explored for a variety of critical photocatalytic applications in the past few years. Nevertheless, CPs for efficient CO2 photoreduction have been rarely reported, which is mainly due to

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