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Naphthalene-1-thiol

CAS No.:
529-36-2
Catalog Number:
AG0032TH
Molecular Formula:
C10H8S
Molecular Weight:
160.2355
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Product Description
Catalog Number:
AG0032TH
Chemical Name:
Naphthalene-1-thiol
CAS Number:
529-36-2
Molecular Formula:
C10H8S
Molecular Weight:
160.2355
MDL Number:
MFCD00039599
IUPAC Name:
naphthalene-1-thiol
InChI:
InChI=1S/C10H8S/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H
InChI Key:
SEXOVMIIVBKGGM-UHFFFAOYSA-N
SMILES:
Sc1cccc2c1cccc2
EC Number:
208-462-7
UNII:
9A78CP495H
Properties
Complexity:
133  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
160.035g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
160.234g/mol
Monoisotopic Mass:
160.035g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.8  
Literature
Title Journal
Shedding light into the detailed excited-state relaxation pathways and reaction mechanisms of thionaphthol isomers. The journal of physical chemistry. A 20110210
SERS-active gold lace nanoshells with built-in hotspots. Nano letters 20101013
Pattern-based recognition of thiols and metals using a single squaraine indicator. Journal of the American Chemical Society 20090916
Site-specific radical directed dissociation of peptides at phosphorylated residues. Journal of the American Chemical Society 20080917
S-S bond mesolysis in alpha,alpha'-dinaphthyl disulfide radical anion generated during gamma-radiolysis and pulse radiolysis in organic solution. The journal of physical chemistry. A 20061221
Non-nucleoside HIV reverse transcriptase inhibitors, Part 6[1]: synthesis and anti-HIV activity of novel 2-[(arylcarbonylmethyl)thio]-6-arylthio DABO analogues. Archiv der Pharmazie 20051001
1,2-Thio group migration in Rh(II) carbene reactions. The Journal of organic chemistry 20050513
Surface-enhanced Raman scattering for ultrasensitive chemical analysis of 1 and 2-naphthalenethiols. The Analyst 20041201
New paeonilactone-A adducts formed by anaerobic incubation of paeoniflorin with Lactobacillus brevis in the presence of arylthiols. Chemical & pharmaceutical bulletin 20010701
Properties