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1-[BROMO(PHENYL)METHYLENE]-2-(2,4-DIBROMOPHENYL)-HYDRAZINE is a chemical compound characterized by the presence of a phenylmethylene group and a hydrazine group, with bromine atoms attached to both the phenyl and dibromophenyl groups. This unique structure and reactivity make it a versatile compound with potential applications in organic synthesis and pharmaceutical development.

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  • 2516-46-3 Structure
  • Basic information

    1. Product Name: 1-[BROMO(PHENYL)METHYLENE]-2-(2,4-DIBROMOPHENYL)-HYDRAZINE
    2. Synonyms: 1-[BROMO(PHENYL)METHYLENE]-2-(2,4-DIBROMOPHENYL)-HYDRAZINE;Benzoyl bromide 2,4-dibromophenylhydrazone;1-[Bromo(phenyl)methylene]-2-(2,4-dibromophenyl)-;1-(2,4-Dibromophenyl)-2-(bromophenylmethylene)hydrazine
    3. CAS NO:2516-46-3
    4. Molecular Formula: C13H9Br3N2
    5. Molecular Weight: 432.94
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2516-46-3.mol
  • Chemical Properties

    1. Melting Point: 110-114°C
    2. Boiling Point: 433.6°Cat760mmHg
    3. Flash Point: 216°C
    4. Appearance: /
    5. Density: 1.86g/cm3
    6. Vapor Pressure: 1.01E-07mmHg at 25°C
    7. Refractive Index: 1.664
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-[BROMO(PHENYL)METHYLENE]-2-(2,4-DIBROMOPHENYL)-HYDRAZINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-[BROMO(PHENYL)METHYLENE]-2-(2,4-DIBROMOPHENYL)-HYDRAZINE(2516-46-3)
    12. EPA Substance Registry System: 1-[BROMO(PHENYL)METHYLENE]-2-(2,4-DIBROMOPHENYL)-HYDRAZINE(2516-46-3)
  • 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: 2516-46-3(Hazardous Substances Data)

2516-46-3 Usage

Uses

Used in Organic Synthesis:
1-[BROMO(PHENYL)METHYLENE]-2-(2,4-DIBROMOPHENYL)-HYDRAZINE is used as a reactive intermediate for various organic synthesis processes due to the increased reactivity provided by the bromine atoms. This allows for the formation of new chemical bonds and the synthesis of complex organic molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 1-[BROMO(PHENYL)METHYLENE]-2-(2,4-DIBROMOPHENYL)-HYDRAZINE is used as a potential building block for drug design and development. The presence of the phenylmethylene and hydrazine groups makes it a promising candidate for the creation of new pharmaceutical compounds with potential therapeutic applications.
Overall, 1-[BROMO(PHENYL)METHYLENE]-2-(2,4-DIBROMOPHENYL)-HYDRAZINE is a versatile chemical compound with potential uses in various fields of chemistry and medicine, including organic synthesis and pharmaceutical development. Its unique structure and reactivity, enhanced by the bromine atoms, make it a valuable asset in the development of new chemical processes and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 2516-46-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2516-46:
(6*2)+(5*5)+(4*1)+(3*6)+(2*4)+(1*6)=73
73 % 10 = 3
So 2516-46-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H9Br3N2/c14-10-6-7-12(11(15)8-10)17-18-13(16)9-4-2-1-3-5-9/h1-8,17H

2516-46-3SDS

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 (Z)-N-(2,4-dibromophenyl)benzenecarbohydrazonoyl bromide

1.2 Other means of identification

Product number -
Other names BENZOYL BROMIDE,2,4-DIBROMOPHENYLHYDRAZONE

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:2516-46-3 SDS

2516-46-3Relevant articles and documents

Lewis acid–catalyzed green synthesis and biological studies of pyrrolo[3,4-c]pyrazoles in aqueous medium

Arjuna, Anania,Kaur, Manpreet,Singh, Baldev

, (2019/12/24)

An environmentally benign approach in aqueous medium by means of Lewis acid catalyst affords a wide spectrum of pyrazoline derivatives in satisfactory yields. [3+2] cycloaddition reactions of substituted azomethine-N-imines to maleimide in aqueous medium at relatively high concentrations of Lewis acid catalyst have emerged as an environment friendly alternative to conventional solvents. Promising catalytic activity has been revealed by Lewis acid like Cu (NO3)2 in aqueous medium. The obvious features of this synthetic protocol were short reaction time, high efficiency, less hazardous synthesis by benign solvent, catalysis, modest workup, and a clean reaction methodology.

1, 3-Dipolar cycloaddition reactions: Synthesis of 5-benzyl-1-(2',4'- dibromophenyl)-3-(4''-substituted phenyl)-3a,4,6,6a-tetrahydro-1H, 5H-pyrrolo[3,4-c]pyrazole-4,6-dione derivatives

Kaur, Manpreet,Singh, Baldev,Singh, Baljit

, p. 1529 - 1534 (2014/04/03)

1,3-Dipolar cycloaddition of nitrilimines 3 with N-benzyl maleimide 4 has provided 5-benzyl-1-(2',4'-dibromophenyl)-3-(4''-substituted phenyl)-3a,4,6,6a-tetrahydro-1H,5H-pyrrolo[3,4-c]pyrazole-4,6-dione derivatives 5 in excellent yield as the only isomer through a concerted pathway. Indian Academy of Sciences.

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