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Key Documents

518883

Sigma-Aldrich

Dichlorodiphenoxymethane

Synonym(s):

Phosgene diphenyl acetal

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About This Item

Linear Formula:
(C6H5O)2CCl2
CAS Number:
Molecular Weight:
269.12
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

mp

39-44 °C (lit.)

SMILES string

ClC(Cl)(Oc1ccccc1)Oc2ccccc2

InChI

1S/C13H10Cl2O2/c14-13(15,16-11-7-3-1-4-8-11)17-12-9-5-2-6-10-12/h1-10H

InChI key

TVIUSKXXXZSVJU-UHFFFAOYSA-N

Application

Reactant for:
  • Cyclocondensation of aminophenols and amines
  • Preparation of LIM-Kinase 2 inhibitors for the treatment of ocular hypertension

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Synthesis and mass spectral fragmentations of new spiro heterocycles.
Rahimizadeh M, et al.
Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao, 18(6), 689-693 (2007)
The synthesis of sulfur-containing spiro orthocarbonates.
Bromley MK, et al.
Australian Journal of Chemistry, 52(7), 657-662 (1999)
Iodine-Catalyzed Synthesis of Spiroorthocarbonates under Neutral Conditions.
Rahimizadeh M, et al.
ChemInform, 41(1), i-i (2010)
The Reactions of Methyl-and n-Butyllithium with Dichloromethyl Methyl Ether and Dichlorodiphenoxymethane.
McDonald RN and Krueger.
The Journal of Organic Chemistry, 30(12), 4372-4375 (1965)
Polyorthocarbonates.
Takekoshi T.
Journal of Polymer Science Part A: Polymer Chemistry, 10(12), 3509-3518 (1972)

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