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About This Item
Linear Formula:
ClCH2CON(CH3)2
CAS Number:
Molecular Weight:
121.57
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-224-4
Beilstein/REAXYS Number:
969568
MDL number:
Assay:
≥97.0% (GC)
Form:
liquid
InChI key
XBPPLECAZBTMMK-UHFFFAOYSA-N
InChI
1S/C4H8ClNO/c1-6(2)4(7)3-5/h3H2,1-2H3
SMILES string
CN(C)C(=O)CCl
assay
≥97.0% (GC)
form
liquid
refractive index
n20/D 1.479
density
1.182 g/mL at 20 °C (lit.)
functional group
amide, chloro
Quality Level
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Application
2-Chloro-N,N-dimethylacetamide (N,N-dimethylchloroacetamide) was used in the synthesis of (S)-carbinoxamine.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
>230.0 °F - closed cup
flash_point_c
> 110 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
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Find documentation for the products that you have recently purchased in the Document Library.
Asymmetric synthesis of (S)-carbinoxamine. New aspects of oxazaborolidine-catalyzed enantioselective carbonyl reduction.
Corey EJ and Helal CJ.
Tetrahedron Letters, 37(32), 5675-5678 (1996)
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