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N,N-Diethylchloroacetamide | CAS:2315-36-8
N,N-Diethylchloroacetamide
  • Name:N,N-Diethylchloroacetamide
  • CAS:2315-36-8
  • Synonyms:2-Chloro-N,N-diethylacetamide
  • Molecular Formula:C6H12ClNO
  • Molecular Weight:149.62
  • EINESC:219-019-2

Description

Properties

Water Solubility soluble
Boiling point 121-122 ºC (12 mmHg)
Density 1.089
Refractive index 1.469-1.471

Safety

Symbol(GHS) T+
Hazard Codes R21/22;R26;R36/37/38
SDS/MSDS S26;S28A;S36/37/39;S38;S45

SDS

Source SDS/MSDS Samples
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Peer-Reviewed Papers
Synthesis and Characterization of Specific Reverse Transcriptase Inhibitors for Mammalian LINE-1 Retrotransposons.Guillermo Banuelos-Sanchez et al.Cell chemical biology, 26(8), 1095-1109 (2019-06-04) 5-Halogeno-3'-fluoro-2',3'-dideoxyuridines as inhibitors of human immunodeficiency virus (HIV): potent and selective anti-HIV activity of 3'-fluoro-2',3'-dideoxy-5-chlorouridine.J Balzarini et al.Molecular pharmacology, 35(5), 571-577 (1989-05-01) 5-Chloro-substituted derivatives of 2', 3'-didehydro-2',3'-dideoxyuridine, 3'-fluoro-2',3'-dideoxyuridine and 3'-azido-2',3'-dideoxyuridine as anti-HIV agents.J Balzarini et al.Biochemical pharmacology, 38(6), 869-874 (1989-03-15) Synthesis and in vitro antiviral activities of 3'-fluoro (or chloro) and 2',3'-difluoro 2',3'-dideoxynucleoside analogs against hepatitis B and C viruses.Naveen C Srivastav et al.Bioorganic & medicinal chemistry, 18(21), 7542-7547 (2010-09-28) Perspectives for the chemotherapy of AIDS.E De Clercq Chemioterapia : international journal of the Mediterranean Society of Chemotherapy, 7(6), 357-364 (1988-12-01) Deoxyuridine triphosphate nucleotidohydrolase as a potential antiparasitic drug targetNguyen C, et al. Journal of Medicinal Chemistry, 48(19), 5942-5954 (2005) Hiyama T Organofluorine Compounds: Chemistry and Applications, 153-153 null Differential patterns of intracellular metabolism of 2',3'-didehydro-2',3'-dideoxythymidine and 3'-azido-2',3'-dideoxythymidine, two potent anti-human immunodeficiency virus compounds.J Balzarini et al.The Journal of biological chemistry, 264(11), 6127-6133 (1989-04-15)
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