127167
3-Chlorobenzylamine
98%
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About This Item
Linear Formula:
ClC6H4CH2NH2
CAS Number:
Molecular Weight:
141.60
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
223-985-0
MDL number:
Product Name
3-Chlorobenzylamine, 98%
InChI key
BJFPYGGTDAYECS-UHFFFAOYSA-N
InChI
1S/C7H8ClN/c8-7-3-1-2-6(4-7)5-9/h1-4H,5,9H2
SMILES string
NCc1cccc(Cl)c1
assay
98%
form
liquid
refractive index
n20/D 1.559 (lit.)
bp
110-112 °C/17 mmHg (lit.)
density
1.159 g/mL at 25 °C (lit.)
functional group
amine
chloro
Quality Level
Related Categories
General description
3-Chlorobenzylamine undergoes reductive amination during dihydroquinolone synthesis. It is used in the synthesis of N- (3-chlorobenzyl) toluene-p-sulphonamide.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
208.4 °F - closed cup
flash_point_c
98 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Rates of reaction of benzylamines with 1-chloro-2, 4-dinitrobenzene and with toluene-p-sulphonyl chloride.
Journal of the Chemical Society B: Physical Organic, 466-468 (1966)
Stefan Jaroch et al.
Bioorganic & medicinal chemistry letters, 13(12), 1981-1984 (2003-06-05)
Dihydroquinolines with aminoalkyl side chains have been synthesized and have been shown to be potent n-NOS inhibitors. A marked selectivity versus e-NOS of up to approximately 300-fold was observed, whereas i-NOS was moderately inhibited.
E Farcaş et al.
Analytica chimica acta, 1034, 214-222 (2018-09-09)
Only few reports describe the use of capillary electrophoresis in the context of Fragment Based Drug Discovery (FBDD). In this paper, we will present a generic, fully automated, microscale electrophoretic mobility shift displacement assay that can be used in FBDD
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