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Phthalylglycyl chloride_Molecular_structure_CAS_6780-38-7)
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Phthalylglycyl chloride

Catalog No. 636401 Name Sigma Aldrich
CAS Number 6780-38-7 Website http://www.sigmaaldrich.com
M. F. C10H6ClNO3 Telephone 1-800-521-8956
M. W. 223.61254 Fax
Purity 96% Email
Storage Chembase ID: 60225

SYNONYMS

Title
N-邻苯二甲酰甘氨酰氯
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
Phthalylglycine acid chloride
1,3-Dioxo-2-isoindolineacetyl chloride
NSC 401729

DATABASE IDS

PubChem SID 24882779
CAS Number 6780-38-7
EC Number 229-840-8
MDL Number MFCD00192872

PROPERTIES

Empirical Formula (Hill Notation) C10H6ClNO3
Purity 96%
GHS Pictograms GHS05
GHS Pictograms GHS06
GHS Signal Word Danger
GHS Hazard statements H301-H314
European Hazard Symbols Toxic Toxic (T)
MSDS Link Download
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
GHS Precautionary statements P280-P305 + P351 + P338-P310
RID/ADR UN 2923 8/PG 3
Risk Statements 25-34
Safety Statements 26-36/37/39-45
Hazard Class 8
UN Number 2923
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
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
Description (简体中文)
包装
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

REFERENCES