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Benzoic acid, 2-bromo-,2-(2-bromobenzoyl)hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50796-71-9

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50796-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50796-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,9 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 50796-71:
(7*5)+(6*0)+(5*7)+(4*9)+(3*6)+(2*7)+(1*1)=139
139 % 10 = 9
So 50796-71-9 is a valid CAS Registry Number.

50796-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-N'-(2-bromobenzoyl)benzohydrazide

1.2 Other means of identification

Product number -
Other names 2-(2-bromobenzoyl)hydrazide

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:50796-71-9 SDS

50796-71-9Relevant academic research and scientific papers

ORGANIC COMPOUNDS AND ORGANIC ELECTRO LUMINESCENCE DEVICE COMPRISING THE SAME

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Paragraph 0110; 0130; 0131; 0132, (2016/10/08)

The present invention relates to a novel organic compound and an organic electroluminescent device comprising the same. The organic electroluminescent device with improved luminous efficiency, driving voltage, and service life can be provided by introducing a light emitting layer using a triazolebiscarbazole-based compound as a host material to the organic electroluminescent device.

2,5-Bis(2-(diphenylphosphino)phenyl)-1,3,4-oxadiazole ligands and their Cu(I) complexes for Sonogashira coupling reaction

Lin, Cai-Xia,Zhu, Jia-Fang,Li, Qing-Shan,Ao, Li-Hua,Jin, Yan-Juan,Xu, Feng-Bo,Hu, Fang-Zhong,Yuan, Yao-Feng

, p. 298 - 303 (2014/04/03)

Two diphosphane ligands - 2,5-bis(2-(diphenylphosphino)-5-R)phenyl)-1,3,4- oxadiazole (L1, R = H, L2, R = OMe) and their binuclear complexes, L1Cu and L2Cu, were prepared and characterized. The molecular structures of L1Cu and L2Cu, as perchlorate salts,

Benzo[a]acecorannulene: Surprising formation of a new bowl-shaped aromatic hydrocarbon from an attempted synthesis of 1,2-diazadibenzo[d,m]corannulene

Tsefrikas, Vikki M.,Arns, Steve,Merner, Patrick M.,Warford, C. Chad,Merner, Bradley L.,Scott, Lawrence T.,Bodwell, Graham J.

, p. 5195 - 5198 (2007/10/03)

Flash vacuum pyrolysis of 7,10-bis(2-bromophenyl)acenaphtho[1,2-d] pyridazine (C26H14Br2N2) has resulted in a surprising transformation, including dinitrogen loss, to give benzo[a]acecorannulene, a novel C2

Microwave-induced conversion of acid hydrazides to N,N′- diacylhydrazines in solvent-free conditions

Sailu,Komaraiah,Reddy

, p. 1907 - 1910 (2007/10/03)

A new and efficient method of converting acid hydrazides 1 to the corresponding N,N′-diacylhydrazines 2 under microwave irradiation and in solvent-free conditions has been described. Copyright Taylor & Francis Group, LLC.

Syntheses and insecticidal activities of novel 2,5-disubstituted 1,3,4-oxadiazoles

Zheng, Xiumian,Li, Zhong,Wang, Yanli,Chen, Weidong,Huang, Qingchun,Liu, Chuanxiang,Song, Gonghua

, p. 163 - 169 (2007/10/03)

Nine novel symmetrical and asymmetrical 2,5-disubstituted 1,3,4-oxadiazoles have been synthesized by a facile and mild method with high yield. Meantime, it was found that the fluorine was easy substituted by hydrazine in polyhalogen-substituted aroyl hydrazine. The preliminary bioassay tests show that two of the compounds (D5> and D6) exhibited a significant insecticidal activity (LC50=116.02 and 70.93 mg l-1) on armyworm, Leucania separata Walker. Using the Drug Discovery Workbench (DDW) (Cerius2), structure-activities relationship was studied.

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