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About This Item
Linear Formula:
H2NC6H4CH2OH
CAS Number:
Molecular Weight:
123.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-514-8
Beilstein/REAXYS Number:
2205844
MDL number:
Assay:
97%
Form:
solid
Product Name
3-Aminobenzyl alcohol, 97%
InChI key
OJZQOQNSUZLSMV-UHFFFAOYSA-N
InChI
1S/C7H9NO/c8-7-3-1-2-6(4-7)5-9/h1-4,9H,5,8H2
SMILES string
Nc1cccc(CO)c1
assay
97%
form
solid
mp
92-95 °C (lit.)
functional group
hydroxyl
Quality Level
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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Nicolas Bridiau et al.
Biotechnology progress, 22(1), 326-330 (2006-02-04)
A new approach to galacto-oligosaccharides and galacto-conjugates synthesis performed by the beta-galactosidase from Kluyveromyces lactis is reported. The enzymatic galactosylation of eight kinds of adsorbed aromatic primary alcohols, in particular the two drugs guaifenesin and chlorphenesin, gave the corresponding beta-D-galacto-pyranosides
Synthesis and fungicidal activity of N-[4-(4-fluoro) phenyl-2-piperidin-4-yl-thiazol-5-yl] pyrimidin-2-yl-N-phenylamines on Phytophthora capsici.
Choi W-S, et al.
Journal of the Korean Society for Applied Biological Chemistry, 53(2), 206-214 (2010)
Synthesis and characterization of new 2-(alkylamino) acetamides.
Mancilla T, et al.
ARKIVOC (Gainesville, FL, United States), 11, 37-47 (2003)
N Sundaraganesan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 59(11), 2511-2517 (2003-09-10)
The laser Raman and FTIR spectra of 3-aminobenzyl alcohol have been recorded. The observed frequencies were assigned to various modes of vibrations on the basis of normal coordinate analysis, assuming C(s) point group symmetry. The potential energy distribution associated with
Anton Georgiev et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 175, 76-91 (2016-12-27)
In this paper three different "push-pull" 4-aminoazobenzene dyes have been synthesized in order to characterize their photochromic behavior in different solvents. The molecular geometry was optimized by DFT/B3LYP functional combined with the standard 6-31+G(d,p) basis set for trans (E) and
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