2835-98-5 | 6-Amino-m-cresol

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$7.00	$5.00
10g	98%	in stock	$12.00	$9.00
25g	98%	in stock	$21.00	$15.00
100g	98%	in stock	$78.00	$55.00

Description

• Catalog Number: AB61130
• Chemical Name: 6-Amino-m-cresol
• CAS Number: 2835-98-5
• Molecular Formula: C7H9NO
• Molecular Weight: 123.1525
• MDL Number: MFCD00007693
• SMILES: Cc1ccc(c(c1)O)N
• NSC Number: 322874

Computed Properties

• Complexity: 94.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• XLogP3: 1.2

Literature

• Peculiarity of methoxy group-substituted phenylhydrazones in Fischer indole synthesis.

  Proceedings of the Japan Academy. Series B, Physical and biological sciences 20120111

• 2-[(Naphthalen-1-yl-methyl-idene)amino]-5-methyl-phenol.

  Acta crystallographica. Section E, Structure reports online 20110901

• 2-Aminophenoxazine-3-one and 2-amino-4,4α-dihydro-4α,7-dimethyl-3H-phenoxazine-3-one cause cellular apoptosis by reducing higher intracellular pH in cancer cells.

  Proceedings of the Japan Academy. Series B, Physical and biological sciences 20110511

• Vibrational spectroscopy investigation using ab initio and density functional theory analysis on the structure of 2-amino-5-methylphenol.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20070601

• Effect of natural phenol derivatives on skeletal type sarcoplasmic reticulum Ca2+ -ATPase and ryanodine receptor.

  Journal of muscle research and cell motility 20070101

• A novel kinetic determination of dissolved chromium species in natural and industrial waste water.

  Talanta 20060915

• Prediction of genotoxicity of chemical compounds by statistical learning methods.

  Chemical research in toxicology 20050601

• Final report on the safety assessment of 6-Amino-m-Cresol, 6-Amino-o-Cresol, 4-Amino-m-Cresol, 5-Amino-4-Chloro-o-Cresol, 5-Amino-6-Chloro-o-Cresol, and 4-Chloro-2-Aminophenol.

  International journal of toxicology 20040101

• Antiviral activity of 2-amino-4,4alpha-dihydro-4alpha-7-dimethyl-3H-phenoxazine-3-one on poliovirus.

  The Tohoku journal of experimental medicine 20030701

• A novel phenoxazine derivative suppresses proliferation of human endometrial adenocarcinoma cell lines, inducing G2M accumulation and apoptosis.

  Oncology reports 20030101

• A novel meta-cleavage dioxygenase that cleaves a carboxyl-group-substituted 2-aminophenol. Purification and characterization of 4-amino-3-hydroxybenzoate 2,3-dioxygenase from Bordetella sp. strain 10d.

  European journal of biochemistry 20021201

• Antitumor activity of a phenoxazine compound, 2-amino-4,4alpha-dihydro-4alpha,7-dimethyl-3H-phenoxazine-3-one against human B cell and T cell lymphoblastoid cell lines: induction of mixed types of cell death, apoptosis, and necrosis.

  Journal of cancer research and clinical oncology 20020701

• An improved method for the rapid preparation of 2-amino-4,4a-dihydro-4a,7-dimethyl-3H-phenoxazine-3-one, a novel antitumor agent.

  Bioorganic & medicinal chemistry letters 20010423

• Prevention of growth of human lung carcinoma cells and induction of apoptosis by a novel phenoxazinone, 2-amino-4,4alpha-dihydro-4alpha,7-dimethyl-3H-phenoxazine-3-one.

  Anti-cancer drugs 20010401

• Antitumor effects of a novel phenoxazine derivative on human leukemia cell lines in vitro and in vivo.

  Clinical cancer research : an official journal of the American Association for Cancer Research 20010301