2243-47-2 | 3-Aminobiphenyl

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$5.00	$4.00
5g	98%	in stock	$9.00	$7.00
10g	98%	in stock	$11.00	$8.00
25g	98%	in stock	$21.00	$15.00
100g	98%	in stock	$83.00	$59.00

Description

• Catalog Number: AB64297
• Chemical Name: 3-Aminobiphenyl
• CAS Number: 2243-47-2
• Molecular Formula: C12H11N
• Molecular Weight: 169.2224
• MDL Number: MFCD00047846
• SMILES: Nc1cccc(c1)c1ccccc1

Computed Properties

• Complexity: 149
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 3.3

Upstream Synthesis Route

3-Aminobiphenyl is a versatile compound widely utilized in chemical synthesis for its reactivity and selective properties. In organic chemistry, 3-aminobiphenyl serves as a crucial building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its amino group allows for facile derivatization and incorporation into complex molecular structures. This compound is often employed as a key intermediate in the preparation of dyes, optical brighteners, and advanced materials. Additionally, 3-aminobiphenyl plays a significant role in the development of novel catalysts and functional materials due to its ability to participate in diverse chemical reactions. Its unique structural features make it a valuable starting material for the creation of diverse molecular scaffolds, making it an indispensable resource for the field of chemical synthesis.

Literature

• Inhibition of monoamine oxidase by selected C5- and C6-substituted isatin analogues.

  Bioorganic & medicinal chemistry 20110101

• Analysis of 4-aminobiphenyl hemoglobin adducts in smokers and nonsmokers by pseudo capillary on-column gas chromatography- tandem mass spectrometry.

  Journal of analytical toxicology 20100101

• Voltammetric determination of aminobiphenyls at a boron-doped nanocrystalline diamond film electrode.

  Talanta 20071215

• CYP1A2 and NAT2 phenotyping and 3-aminobiphenyl and 4-aminobiphenyl hemoglobin adduct levels in smokers and non-smokers.

  Toxicology and applied pharmacology 20060615

• Carotenoids/vitamin C and smoking-related bladder cancer.

  International journal of cancer 20040620

• Identification of DNA adducts using HPLC/MS/MS following in vitro and in vivo experiments with arylamines and nitroarenes.

  Chemical research in toxicology 20031001

• Nonsmoking-related arylamine exposure and bladder cancer risk.

  Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 20030601

• Growth inhibition of intestinal bacteria and mutagenicity of 2-, 3-, 4-aminobiphenyls, benzidine, and biphenyl.

  Toxicology in vitro : an international journal published in association with BIBRA 20030401

• Unusual luminescence characteristics of aminobiphenyls.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20021101

• Gender- and smoking-related bladder cancer risk.

  Journal of the National Cancer Institute 20010404