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(3,5-Dibromo-phenyl)hydrazine, also known as 3,5-Dibromophenylhydrazine, is a hydrazine derivative with the molecular formula C6H5N2Br2. It is a yellow to brown solid that is used as a reagent in organic synthesis. This chemical compound is commonly utilized in the pharmaceutical and chemical industries due to its versatile reactivity and potential applications.
Used in Pharmaceutical Industry:
(3,5-Dibromo-phenyl)hydrazine is used as a synthetic intermediate for the development of various pharmaceutical compounds. Its unique structure allows it to be a key component in the synthesis of drugs with specific therapeutic properties.
Used in Chemical Industry:
In the chemical industry, (3,5-Dibromo-phenyl)hydrazine serves as a reagent in organic synthesis processes. Its ability to participate in various chemical reactions makes it valuable for creating a range of chemical products.
Used in Research and Development:
(3,5-Dibromo-phenyl)hydrazine is also used in research and development settings to explore its potential applications and to study its chemical properties. This can lead to the discovery of new uses and improvements in existing processes.

861597-19-5

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861597-19-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 861597-19-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,1,5,9 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 861597-19:
(8*8)+(7*6)+(6*1)+(5*5)+(4*9)+(3*7)+(2*1)+(1*9)=205
205 % 10 = 5
So 861597-19-5 is a valid CAS Registry Number.

861597-19-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,5-Dibromophenyl)hydrazine

1.2 Other means of identification

Product number -
Other names QC-935

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:861597-19-5 SDS

861597-19-5Upstream product

861597-19-5Downstream Products

861597-19-5Relevant academic research and scientific papers

Discovery of (S)-3-(3-(3,5-Dimethyl-1 H-pyrazol-1-yl)phenyl)-4-((R)-3-(2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethyl)pyrrolidin-1-yl)butanoic Acid, a Nonpeptidic αvβ6 Integrin Inhibitor for the Inhaled Treatment of Idiopathic Pulmonary Fibrosis

Procopiou, Panayiotis A.,Anderson, Niall A.,Barrett, John,Barrett, Tim N.,Crawford, Matthew H. J.,Fallon, Brendan J.,Hancock, Ashley P.,Le, Joelle,Lemma, Seble,Marshall, Richard P.,Morrell, Josie,Pritchard, John M.,Rowedder, James E.,Saklatvala, Paula,Slack, Robert J.,Sollis, Steven L.,Suckling, Colin J.,Thorp, Lee R.,Vitulli, Giovanni,Macdonald, Simon J. F.

, p. 8417 - 8443 (2018/09/25)

A series of 3-aryl(pyrrolidin-1-yl)butanoic acids were synthesized using a diastereoselective route, via a rhodium catalyzed asymmetric 1,4-addition of arylboronic acids in the presence of (R)-BINAP to a crotonate ester to provide the (S) absolute configuration for the major product. A variety of aryl substituents including morpholine, pyrazole, triazole, imidazole, and cyclic ether were screened in cell adhesion assays for affinity against αvβ1, αvβ3, αvβ5, αvβ6, and αvβ8 integrins. Numerous analogs with high affinity and selectivity for the αvβ6 integrin were identified. The analog (S)-3-(3-(3,5-dimethyl-1H-pyrazol-1-yl)phenyl)-4-((R)-3-(2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethyl)pyrrolidin-1-yl)butanoic acid hydrochloride salt was found to have very high affinity for αvβ6 integrin in a radioligand binding assay (pKi = 11), a long dissociation half-life (7 h), very high solubility in saline at pH 7 (>71 mg/mL), and pharmacokinetic properties commensurate with inhaled dosing by nebulization. It was selected for further clinical investigation as a potential therapeutic agent for the treatment of idiopathic pulmonary fibrosis.

Process for producing 3-anilino-5-pyrazolones

-

, (2008/06/13)

A process for producing a 3-anilino-5-pyrazolone which comprises reacting a β-anilino-β-alkoxy-acrylate with a hydrazine in the presence of a compound having a pKa of about 8 up to about 14.

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