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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:
20780-76-1
Molecular Weight:
273.03
EC Number:
244-035-1
MDL number:
MFCD00016899
UNSPSC Code:
12352100
PubChem Substance ID:
24848473
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

Related Categories

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
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H317,H319,H335

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

140589-BULK:
140589-25G:4548173992679
140589-5G:4548173992686
140589-VAR:

Certificates of Analysis (COA)

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

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