Isoindoline
Isoindoline Basic information
- Product Name:
- Isoindoline
- Synonyms:
-
- 1,3-Dihydro-2H-isoindole
- o-Xyleneimine
- 1H-Isoindole, 2,3-dihydro-
- 4-aMino-6-broMo-5-fluoropyriMidine
- Isoinodoline
- Isoindoline 97%
- DIHYDROISOINDOLE
- ISOINDOLINE
- CAS:
- 496-12-8
- MF:
- C8H9N
- MW:
- 119.16
- Product Categories:
-
- Building Blocks
- C7 to C9
- Building Blocks
- Heterocyclic Building Blocks
- Chemical Synthesis
- Heterocyclic Building Blocks
- Indoles
- Mol File:
- 496-12-8.mol
Isoindoline Chemical Properties
- Melting point:
- 17 °C (lit.)
- Boiling point:
- 221 °C (lit.)
- Density
- 1.05 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.57(lit.)
- Flash point:
- 202 °F
- storage temp.
- 2-8°C
- form
- Crystalline Powder, Crystals or Flakes, Darkening On Exposure To Light
- pka
- 9.26±0.20(Predicted)
- color
- White to off-white
- InChIKey
- GWVMLCQWXVFZCN-UHFFFAOYSA-N
- CAS DataBase Reference
- 496-12-8(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
Isoindoline Usage And Synthesis
Description
Isoindoline can be considered as the “hydrogenated sister” of isoindole which is widespread in nature as heterocyclic core of alkaloids and antibiotics.
Uses
Isoindoline is used to make a chiral diamine catalyst from L-proline for the asymmetric acylation of alcohols.1
Uses
Isoindolinone and isoindoline pigments are high quality products. They are used in general and high grade industrial paints including original automobile and automotive refinishes, in plastics and for spin dyeing, and in high grade printing inks, especially for metal deco, laminated plastic sheets, and in printing inks for bank notes and securities.
Synthesis Reference(s)
The Journal of Organic Chemistry, 53, p. 5381, 1988 DOI: 10.1021/jo00257a041
Synthetic Communications, 18, p. 2055, 1988 DOI: 10.1080/00397918808068274
Isoindoline Preparation Products And Raw materials
Preparation Products
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Isoindoline(496-12-8)Related Product Information
- Methylchloroisothiazolinone/methylisothiazolinone mixture (MCIT/MIT)
- Indole
- 2-Methyl-4-isothiazolin-3-one
- Indoline
- Indometacin
- 3,5-Diisopropylbenzene hydroperoxide
- Dihydromyrcenol
- Indole-3-acetic acid
- Indole-3-butyric acid
- cis-Octahydroisoindole
- 2,3-Dihydroisoindole hydrochloride
- ISOINDOLIN-1-ONE
- ISOINDOLINE-5-CARBONITRILE
- PHTHALIMIDE DBU SALT
- Methyl isonicotinate
- ETHYL ISONICOTINOYLACETATE
- METHYL ISONICOTINATE
- Ethyl isonicotinate