518883
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
Recommended Products
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
230.0 °F - closed cup
Flash Point(C)
110 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Polyorthocarbonates.
Takekoshi T.
Journal of Polymer Science Part A: Polymer Chemistry, 10(12), 3509-3518 (1972)
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)
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