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Hydrazine, (4-biphenylyl)-, hydrochloride, with the molecular formula C12H13N2·HCl, is a chemical compound derived from hydrazine and classified under the organic compounds known as biphenyls and their derivatives. Hydrazine, (4-biphenylyl)-, hydrochloride is utilized in various industrial and research settings, such as a reagent in organic synthesis and as a component in the creation of pharmaceuticals and agrochemicals. Due to its toxic nature and potential to cause skin, eye, and respiratory irritation, it requires careful handling, storage in well-ventilated areas, and adherence to safety protocols.

63543-02-2

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63543-02-2 Usage

Uses

Used in Organic Synthesis:
Hydrazine, (4-biphenylyl)-, hydrochloride is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Hydrazine, (4-biphenylyl)-, hydrochloride is used as a building block for the production of certain drugs, leveraging its chemical properties to create medicinal compounds.
Used in Agrochemical Production:
Similarly, in agrochemical manufacturing, Hydrazine, (4-biphenylyl)-, hydrochloride is utilized as a precursor to develop substances that aid in crop protection and enhancement of agricultural yields.

Check Digit Verification of cas no

The CAS Registry Mumber 63543-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,4 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63543-02:
(7*6)+(6*3)+(5*5)+(4*4)+(3*3)+(2*0)+(1*2)=112
112 % 10 = 2
So 63543-02-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2/c13-14-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9,14H,13H2

63543-02-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-phenylphenyl)hydrazine,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-hydrazinobiphenyl hydrochloride

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:63543-02-2 SDS

63543-02-2Relevant academic research and scientific papers

Synthesis of Aryl Hydrazines via CuI/BMPO Catalyzed Cross-Coupling of Aryl Halides with Hydrazine Hydrate in Water

Kumar, Siripuram Vijay,Ma, Dawei

supporting information, p. 1003 - 1006 (2018/09/20)

The N,N’-bis(2,6-dimethylphenyl)oxalamide was discovered as a powerful ligand for Cu-catalyzed cross-coupling of aryl halides with hydrazine hydrate, leading to the formation of a variety of aryl hydrazines at 80 oC in water under the assistance of K3PO4 and 4 mol% cetyltrimethylammonium bromide from aryl bromides and aryl iodides. Good to excellent yields were observed in most cases.

Indole synthesis by rhodium(III)-catalyzed hydrazine-directed C-H activation: Redox-neutral and traceless by N-N bond cleavage

Zhao, Dongbing,Shi, Zhuangzhi,Glorius, Frank

supporting information, p. 12426 - 12429 (2013/12/04)

Fishing for complements! There is an alternative to the useful Fischer indole synthesis. The new method utilizes the same retrosynthetic disconnection but is based on a RhIII-catalyzed directed C-H activation step and a successive coupling with alkynes. Copyright

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