4780-79-4 | 1-Naphthalenemethanol

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$9.00	$6.00
10g	98%	in stock	$15.00	$10.00
25g	98%	in stock	$22.00	$15.00

Description

• Catalog Number: AI50891
• Chemical Name: 1-Naphthalenemethanol
• CAS Number: 4780-79-4
• Molecular Formula: C11H10O
• Molecular Weight: 158.1965
• MDL Number: MFCD00004044
• SMILES: OCc1cccc2c1cccc2
• NSC Number: 5315

Computed Properties

• Complexity: 144
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.4

Literature

• {3,14-Dimethyl-2,6,13,17-tetra-aza-tricyclo-[16.4.0.0]docosane-κN,N',N'',N''')bis-(nitrato-κO)copper(II).

  Acta crystallographica. Section E, Structure reports online 20120201

• β-D-xylosides stimulate GAG synthesis in chondrocyte cultures due to elevation of the extracellular GAG domains, accompanied by the depletion of the intra-pericellular GAG pools, with alterations in the GAG profiles.

  Connective tissue research 20120101

• 3,14-Dimethyl-2,6,13,17-tetra-aza-tricyclo-[16.4.0.0]docosa-ne-(naphthalen-1-yl)methanol (1/2).

  Acta crystallographica. Section E, Structure reports online 20120101

• Antimicrobial Effects of a Lipophilic Fraction and Kaurenoic Acid Isolated from the Root Bark Extracts of Annona senegalensis.

  Evidence-based complementary and alternative medicine : eCAM 20120101

• Mycosporine-like amino acids: relevant secondary metabolites. Chemical and ecological aspects.

  Marine drugs 20110101

• Stepwise photocleavage of C-O bonds of bis(substituted-methyl)naphthalenes with stepwise excitation by two-color two-laser and three-color three-laser irradiations.

  The journal of physical chemistry. A 20050505

• Stepwise photocleavage of two C-O bonds of 1,8-bis[(4-benzoylphenoxy)-methyl]naphthalene with three-step excitation using three-color, three-laser flash photolysis.

  Journal of the American Chemical Society 20040623

• Rapid cleavage of the naphthylmethyl-oxygen bond in higher triplet excited states.

  Chemical communications (Cambridge, England) 20031021

• Comparative molecular field analysis of substrates for an aryl sulfotransferase based on catalytic mechanism and protein homology modeling.

  Journal of medicinal chemistry 20021205

• Evidence for the involvement of multiple pathways in the biodegradation of 1- and 2-methylnaphthalene by Pseudomonas putida CSV86.

  Archives of microbiology 19940101