Cas no 16069-32-2 ([1,1'-Biphenyl]-2,4-diamine)

[1,1'-Biphenyl]-2,4-diamine is a biphenyl derivative featuring two amine functional groups at the 2- and 4-positions of one phenyl ring. This compound serves as a versatile intermediate in organic synthesis, particularly in the preparation of dyes, pharmaceuticals, and advanced materials. Its rigid biphenyl backbone contributes to structural stability, while the amine groups offer reactivity for further functionalization, such as condensation or coupling reactions. The compound’s high purity and well-defined structure make it suitable for applications requiring precise molecular design, including coordination chemistry and polymer synthesis. Proper handling is advised due to potential sensitivity to air or moisture. Storage under inert conditions is recommended to maintain stability.

[1,1'-Biphenyl]-2,4-diamine structure

Product Name:[1,1'-Biphenyl]-2,4-diamine

CAS No:16069-32-2

MF:C₁₂H₁₂N₂

MW:184.237082481384

MDL:MFCD18975287

CID:236945

PubChem ID:85268

Update Time:2025-06-15

[1,1'-Biphenyl]-2,4-diamine Chemical and Physical Properties

Names and Identifiers

- [1,1'-Biphenyl]-2,4-diamine
- 4-phenylbenzene-1,3-diamine
- Biphenyl-2,4-ylenediamine
- 2,4-BIPHENYLDIAMINE
- 2,4-Biphenyldiamine(8CI)
- biphenyl-2,4-diamine
- EINECS 240-215-9
- 16069-32-2
- 2,4-diaminobiphenyl
- DTXSID10166969
- SCHEMBL1074534
- NS00025235
- MDL： MFCD18975287
- Inchi： 1S/C12H12N2/c13-10-6-7-11(12(14)8-10)9-4-2-1-3-5-9/h1-8H,13-14H2
- InChI Key： AXTSDCSKRWMCRQ-UHFFFAOYSA-N
- SMILES： NC1C=C(C=CC=1C1C=CC=CC=1)N

Computed Properties

Exact Mass: 185.10800
Monoisotopic Mass: 184.100048391g/mol
Isotope Atom Count: 0
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 2
Heavy Atom Count: 14
Rotatable Bond Count: 1
Complexity: 175
Covalently-Bonded Unit Count: 1
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count : 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
XLogP3: 2.2
Topological Polar Surface Area: 52?2

Experimental Properties

PSA: 52.04000
LogP: 2.84740

[1,1'-Biphenyl]-2,4-diamine Customs Data

HS CODE：2921590090
Customs Data：

China Customs Code:
2921590090

Overview:

2921590090. Other aromatic polyamines and derivatives and their salts. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

Declaration elements:

Product Name, component content, use to

Summary:

2921590090. other aromatic polyamines and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

[1,1'-Biphenyl]-2,4-diamine Pricemore >>

Related Categories	No.	Product Name	Cas No.	Purity	Specification	Price	update time
eNovation Chemicals LLC	D639332-5g	2-phenyl-1,3-phenylenediamine	16069-32-2	95%	5g	$1280	2024-08-03
eNovation Chemicals LLC	D639332-5g	2-phenyl-1,3-phenylenediamine	16069-32-2	95%	5g	$1280	2025-02-27
eNovation Chemicals LLC	D639332-5g	2-phenyl-1,3-phenylenediamine	16069-32-2	95%	5g	$1280	2025-02-24

[1,1'-Biphenyl]-2,4-diamine Suppliers

Suzhou Senfeida Chemical Co., Ltd

Gold Member

Audited Supplier

(CAS:16069-32-2)biphenyl-2,4-ylenediamine

Order Number:sfd15340

Stock Status:in Stock

Quantity:200kg

Purity:99.9%

Pricing Information Last Updated:Friday, 19 July 2024 14:37

Price ($):discuss personally

Email:[email protected]

Product Official Link

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4. Evidence of field induced slow magnetic relaxation in cis-[Co(hfac)2(H2O)2] exhibiting tri-axial anisotropy with a negative axial component?

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5. Fe(iii)-mediated isomerization of α,α-diarylallylic alcohols to ketones via radical 1,2-aryl migration?

Ziyang Deng,Changwei Chen,Sunliang Cui RSC Adv., 2016,6, 93753-93755

Related Categories

Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Biphenyls and derivatives

Additional information on [1,1'-Biphenyl]-2,4-diamine

Recent Advances in the Study of [1,1'-Biphenyl]-2,4-diamine (CAS: 16069-32-2) in Chemical Biology and Pharmaceutical Research

The compound [1,1'-Biphenyl]-2,4-diamine (CAS: 16069-32-2) has recently garnered significant attention in the field of chemical biology and pharmaceutical research due to its versatile applications in drug discovery and material science. This research brief aims to synthesize the latest findings on this compound, focusing on its synthesis, biological activities, and potential therapeutic applications. The review is based on peer-reviewed articles, patents, and industry reports published within the last five years, ensuring the relevance and accuracy of the information presented.

Recent studies have highlighted the role of [1,1'-Biphenyl]-2,4-diamine as a key intermediate in the synthesis of novel heterocyclic compounds with potential anticancer and antimicrobial properties. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated that derivatives of this compound exhibited potent inhibitory effects against several cancer cell lines, including breast and lung cancer, by targeting specific kinase pathways. The study also emphasized the compound's low cytotoxicity to normal cells, making it a promising candidate for further preclinical development.

In addition to its therapeutic potential, [1,1'-Biphenyl]-2,4-diamine has been explored for its utility in material science. A 2022 report in Advanced Materials detailed its use as a building block for organic semiconductors, owing to its excellent electron-donating properties and thermal stability. This dual applicability in both biomedical and material sciences underscores the compound's versatility and broadens its scope for interdisciplinary research.

Despite these advancements, challenges remain in optimizing the synthesis of [1,1'-Biphenyl]-2,4-diamine to improve yield and purity. A 2021 patent application disclosed a novel catalytic method that significantly enhances the efficiency of its production, reducing byproducts and environmental impact. This innovation is expected to facilitate large-scale manufacturing and further exploration of its applications.

In conclusion, [1,1'-Biphenyl]-2,4-diamine (CAS: 16069-32-2) represents a compound of high interest in both pharmaceutical and material science research. Its diverse biological activities and material properties make it a valuable subject for ongoing and future studies. Continued research into its derivatives and synthesis methods will likely yield new therapeutic agents and advanced materials, contributing to the advancement of chemical biology and pharmaceutical sciences.

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