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化驗
96%
mp
188-198 °C (lit.)
SMILES 字串
ClN1C(=O)c2ccccc2C1=O
InChI
1S/C8H4ClNO2/c9-10-7(11)5-3-1-2-4-6(5)8(10)12/h1-4H
InChI 密鑰
WDRFYIPWHMGQPN-UHFFFAOYSA-N
一般說明
N-Chlorophthalimide in anhydrous acetic acid serves as a useful oxidizing reagent for use in various direct titrimetric analyses. N-Chlorophthalimide can be synthesized by reacting phthalimide, t-butyl hypochlorite, water and t-butyl alcohol. It participates in the synthesis of 2-amino-3-benzoyl-α-(methylthio)phenylacetamide.
應用
N-Chlorophthalimide may be employed in the synthesis of:
- α-amino acetal
- α-amino nitro compounds
- vicinal diamine
- α,β-unsaturated vicinal haloamino nitro compound
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 1
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Talanta, 32(11), 1067-1068 (1985-11-01)
A stable new oxidimetric titrant, N-chlorophthalimide in anhydrous acetic acid, is proposed for direct titrations of a variety of simple and complex reductants such as As(III), Sb(III), Fe(II), ferrocyanide, iodide, ascorbic acid, hydroquinone, hydrazine, phenylhydrazine, benzhydrazide, isonicotinic acid hydrazide, semicarbazide
Development and a practical synthesis of nepafenac intermediate via modified Gassman reaction.
Letters in Organic Chemistry, 9(7), 461-464 (2012)
Aminochlorination reaction with N-chlorophthalimide as a new nitrogen/chlorine source resulting in a-amino derivatives.
Tetrahedron, 68(31), 6198-6203 (2012)
N-Chlorophthalimide as a mild and efficient chlorination reagent in the Gassman ortho alkylation of aromatic amines. Synthesis of 3-(methylthio) oxindoles.
Tetrahedron Letters, 55(40), 5423-5425 (2014)
Tertiary Butyl Hypochlorite as as N-Chlorinating Agent.
Journal of the American Chemical Society, 76(14), 3856-3857 (1954)
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