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140589

Sigma-Aldrich

5-Iodoisatin

technical grade

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About This Item

Empirical Formula (Hill Notation):
C8H4INO2
CAS Number:
Molecular Weight:
273.03
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical grade

form

solid

mp

276-280 °C (lit.)

SMILES string

Ic1ccc2NC(=O)C(=O)c2c1

InChI

1S/C8H4INO2/c9-4-1-2-6-5(3-4)7(11)8(12)10-6/h1-3H,(H,10,11,12)

InChI key

OEUGDMOJQQLVAZ-UHFFFAOYSA-N

General description

5-Iodoisatin undergoes condensation reaction with:
  • phenol yields 5-iodophenolisatin
  • malonic acid yields 6-iodo-2-quinolone-4-carboxylic acid

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - 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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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THE PREPARATION OF CERTAIN IODINATED DERIVATIVES OF PHENOLISATIN.
Sumpter WC.
Journal of the American Chemical Society, 54(9), 3766-3768 (1932)
CCCLXXXVII.-The relative stability of the quinolone and indolinone rings.
Aeschlimann JA.
Journal of the Chemical Society, 129, 2902-2912 (1926)

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