Substance
ID:320183
Names and Identifiers
IUPAC name
2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)acetyl chloride
IUPAC Traditional name
2-(1,3-dioxoisoindol-2-yl)acetyl chloride
Synonyms
Phthalylglycyl chloride1,3-Dioxo-2-isoindolineacetyl chlorideN-邻苯二甲酰甘氨酰氯NSC 401729Phthalylglycine acid chloride
Properties
Safety Information
Hazard Class
8
UN Number
2923
GHS Precautionary statements
P280-P305+P351+P338-P310
European Hazard Symbols
Toxic (T)Packing Group
3
GHS Signal Word
Danger
RID/ADR
UN 2923 8/PG 3
MSDS Link
German water hazard class
3
GHS Pictograms
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
GHS Hazard statements
H301-H314
Personal Protective Equipment
Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
Safety Statements
26-36/37/39-45
Risk Statements
25-34
Product Information
Empirical Formula (Hill Notation)
C10H6ClNO3
Purity
96%
Molecule Details
Packaging
1 g in glass bottle
Application
Reactant involved in:
• Synthesis of selenium-containing amino acid analogs with bactericidal and antifungal activity1
• Photoinduced single electron transfer cyclization for preparation of cyclic peptides2
• Arndt-Eistert synthesis3
• Mitsunobu and arbuzov-type multicomponent pathway4
• Remote C-H bond functionalization5
• Amido-alkylation for synthesis of benzofuran derivatives6
1 g in glass bottle
Application
Reactant involved in:
• Synthesis of selenium-containing amino acid analogs with bactericidal and antifungal activity1
• Photoinduced single electron transfer cyclization for preparation of cyclic peptides2
• Arndt-Eistert synthesis3
• Mitsunobu and arbuzov-type multicomponent pathway4
• Remote C-H bond functionalization5
• Amido-alkylation for synthesis of benzofuran derivatives6
Molecular Spectra
No Data Available
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References
No Data Available
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