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About This Item
Linear Formula:
C6H5CH2NHCOCH2Cl
CAS Number:
Molecular Weight:
183.63
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
mp
93-96 °C (lit.)
functional group
amide
chloro
phenyl
SMILES string
ClCC(=O)NCc1ccccc1
InChI
1S/C9H10ClNO/c10-6-9(12)11-7-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,11,12)
InChI key
SRAXAXHQMCQHSH-UHFFFAOYSA-N
General description
2-Chloro-N-benzylacetamide can be prepared by reacting benzylamine and chloroacetylchloride.[1]
Application
2-Chloro-N-benzylacetamide may be used in the preparation of:
- 2-[4-(Aryl substituted) piperazin-1-yl]-N-benzylacetamides by reacting with corresponding arylpiperazines.[1]
- N-Methylacetamide and N-benzylacetamide by reacting with di-tert-butyl 1,4,7-triazacyclononane-1,4-diacetate.[2]
- bis[N-Benzyl-2-(quinolin-8-yloxy)acetamide] monohydrate by reacting with 8-hydroxyquinoline.[3]
- N-Benzyl-2-(1H-imidazol-1-yl)acetamide by reacting with imidazole.[4]
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Formation and Characterization of Gallium (III) Complexes with Monoamide Derivatives of 1,4,7-Triazacyclononane-1,4,7-triacetic Acid: A Study of the Dependency of Structure on Reaction pH.
Shetty D, et al.
European Journal of Inorganic Chemistry, 2010(34), 5432-5438 (2010)
Bis [N-benzyl-2-(quinolin-8-yloxy) acetamide] monohydrate.
Wang MS, et al.
Acta Crystallographica Section E, Structure Reports Online, 67(7), o1558-o1558 (2011)
Chiral Variation of a Hybrid Bis (carbene-amido) Ligand System.
Jean-Baptiste dit Dominique F, et al.
Organometallics, 29(13), 2868-2873 (2010)
Synthesis, computational studies and preliminary pharmacological evaluation of 2-[4-(aryl substituted) piperazin-1-yl]-N-benzylacetamides as potential antipsychotics.
Kumar S, et al.
Arabian Journal of Chemistry (2012)
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