9,9-Bis(methoxymethyl)-9H-fluorene

CAS NO.：182121-12-6
Empirical Formula: C17H18O2
Molecular Weight: 254.32
MDL number: MFCD19441380
EINECS: 682-678-3
SAFETY DATA SHEET (SDS)
Update Date: 2025-08-08 17:45:00

What is 9,9-Bis(methoxymethyl)-9H-fluorene?

Description

9,9-Bis(methoxymethyl)-fluorene is a compound involved in the preparation of polypropylene by heterogeneous Ziegler-Natta catalyst.

The Uses of 9,9-Bis(methoxymethyl)-9H-fluorene

9,9-Bis(methoxymethyl)-fluorene is a hydrocarbon organic matter and can be used as pharmaceutical intermediates.

What are the applications of Application

Using 9,9-Bis(methoxymethyl) fluorene as the internal electron donor of Ziegler-Natta catalyst, polypropylene with relatively narrow molecular mass distribution, high isometric and good mechanical properties could be prepared. In addition, the compound can also be used as an intermediate, through polymerization reaction or functional group, applied to materials or drug molecules and other domains. Therefore, the compound has a wide range of applications.

Properties of 9,9-Bis(methoxymethyl)-9H-fluorene

Boiling point:	359.9±15.0 °C(Predicted)
Density	1.083
storage temp.	Sealed in dry,Room Temperature
solubility	Chloroform (Slightly), Methanol (Slightly)
color	White
InChI	InChI=1S/C17H18O2/c1-18-11-17(12-19-2)15-9-5-3-7-13(15)14-8-4-6-10-16(14)17/h3-10H,11-12H2,1-2H3

Safety information for 9,9-Bis(methoxymethyl)-9H-fluorene

Signal word	Warning
Pictogram(s)	Exclamation Mark Irritant GHS07
GHS Hazard Statements	H302:Acute toxicity,oral H315:Skin corrosion/irritation H319:Serious eye damage/eye irritation H335:Specific target organ toxicity, single exposure;Respiratory tract irritation
Precautionary Statement Codes	P261:Avoid breathing dust/fume/gas/mist/vapours/spray. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Computed Descriptors for 9,9-Bis(methoxymethyl)-9H-fluorene

InChIKey	ZWINORFLMHROGF-UHFFFAOYSA-N
SMILES	C1(COC)(COC)C2=C(C=CC=C2)C2=C1C=CC=C2

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