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About This Item
Linear Formula:
ClC6H4CH2NH2
CAS Number:
Molecular Weight:
141.60
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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.)
SMILES string
NCc1cccc(Cl)c1
InChI
1S/C7H8ClN/c8-7-3-1-2-6(4-7)5-9/h1-4H,5,9H2
InChI key
BJFPYGGTDAYECS-UHFFFAOYSA-N
General description
3-Chlorobenzylamine undergoes reductive amination during dihydroquinolone synthesis. It is used in the synthesis of N- (3-chlorobenzyl) toluene-p-sulphonamide.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
208.4 °F - closed cup
Flash Point(C)
98 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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.
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)
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