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(4-BROMO-3-METHYL-PHENYL)-HYDRAZINE is a chemical compound that features a bromine atom, a phenyl ring with a methyl group, and a hydrazine functional group. It is widely recognized for its role in organic synthesis and pharmaceutical research, where it serves as a building block for developing more complex molecules. (4-BROMO-3-METHYL-PHENYL)-HYDRAZINE's unique properties and reactivity contribute to its value in creating new drug candidates and investigating molecular interactions. However, due to its potential toxicity and harmful effects on human health and the environment, careful handling is essential.

90284-70-1

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90284-70-1 Usage

Uses

Used in Pharmaceutical Research:
(4-BROMO-3-METHYL-PHENYL)-HYDRAZINE is utilized as a key intermediate in the synthesis of pharmaceuticals, particularly for creating molecules with potential anticancer and antiviral properties. Its hydrazine derivative nature allows for the development of new drug candidates that can target and combat various diseases.
Used in Organic Synthesis:
In the field of organic synthesis, (4-BROMO-3-METHYL-PHENYL)-HYDRAZINE is employed as a versatile building block for constructing a range of complex organic molecules. Its reactivity and structural features make it an invaluable tool for chemists working on innovative molecular designs and advancing chemical research.
Used in Chemical Research:
(4-BROMO-3-METHYL-PHENYL)-HYDRAZINE is also used in chemical research to understand molecular interactions and develop new methodologies for creating and modifying complex molecules. Its unique properties allow researchers to explore novel pathways and mechanisms in chemical reactions, contributing to the broader understanding of chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 90284-70-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,8 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90284-70:
(7*9)+(6*0)+(5*2)+(4*8)+(3*4)+(2*7)+(1*0)=131
131 % 10 = 1
So 90284-70-1 is a valid CAS Registry Number.

90284-70-1SDS

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 (4-BROMO-3-METHYL-PHENYL)-HYDRAZINE

1.2 Other means of identification

Product number -
Other names -

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:90284-70-1 SDS

90284-70-1Downstream Products

90284-70-1Relevant academic research and scientific papers

Sodium periodate/TEMPO as a selective and efficient system for amine oxidation

Galletti,Martelli,Prandini,Colucci,Giacomini

, p. 9723 - 9730 (2018/03/23)

A new metal-free protocol for promoting oxidation of amines in aqueous-organic medium was developed. NaIO4 and TEMPO as the catalyst emerged as the most efficient and selective system for oxidation of differently substituted benzyl amines to the corresponding benzaldehydes without overoxidation. Unsymmetrical secondary amines underwent selective oxidation only at the benzylic position thus realising an oxidative deprotection of a benzylic group with an easy amine recovery.

Thermal energy storage in a supramolecular assembly of [C6H11NH3]+[CF3COO]-(C6H11 = cyclohexyl)

Guo, Jiangbin,Tang, Wen,Wu, Binbin,Zhao, Haixia,Long, Lasheng,Zheng, Lansun

, p. 12616 - 12620 (2015/06/25)

A supramolecular compound [C6H11NH3]+[CF3COO]- was synthesized. Investigation on the structure of 1 at different temperatures reveals that it is the disorder of the anions that plays a key role in thermal energy storage. Studies on the thermal and physical properties of 1 indicate that utilization of the sensible heat in 1 can significantly enhance its ability to store thermal energy.

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