All Photos(1)
Synonym(s):
Malonyl dichloride
Linear Formula:
CH2(COCl)2
CAS Number:
Molecular Weight:
140.95
Beilstein:
774044
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
97%
refractive index
n20/D 1.465 (lit.)
bp
53-55 °C/19 mmHg (lit.)
density
1.449 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
ClC(=O)CC(Cl)=O
InChI
1S/C3H2Cl2O2/c4-2(6)1-3(5)7/h1H2
InChI key
SXYFKXOFMCIXQW-UHFFFAOYSA-N
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Related Categories
Application
Malonyl chloride can be used as a reactant for the synthesis of:
It can also be used as a coupling agent in the synthesis of block copolymers by anionic polymerization.
- Alkaloids with tetracyclic cores such as cyclopiamide A and speradine E.
- 6-tetrathiafulvalene(TTF)-polymer by condensation polymerization with TTF-based dihydroxy monomer.
- N-doped TiO2 films by molecular layer deposition.
- Alkyne-substituted 1,3-oxazines by reaction with arylpropynamides.
It can also be used as a coupling agent in the synthesis of block copolymers by anionic polymerization.
accessory
Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 3 - Skin Corr. 1B
Supplementary Hazards
WGK
WGK 1
Flash Point(F)
116.6 °F
Flash Point(C)
47 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
Certificates of Analysis (COA)
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Total synthesis of cyclopiamide A and speradine E
Nakhla MC, et al.
Tetrahedron, 74(38), 5085-5088 (2018)
Nanoporous Nitrogen-Doped Titanium Dioxide with Excellent Photocatalytic Activity under Visible Light Irradiation Produced by Molecular Layer Deposition
Chen C, et al.
Angewandte Chemie (International Edition in English), 125(35), 9366-9370 (2013)
Synthesis and Characterization of a Tetrathiafulvalene-Based Polymer
Lee SH, et al.
Bull. Korean Chem. Soc., 33(5), 1451-1456 (2012)
Preparation of Arylpropynamides and Their Reaction with Malonyl Acid Derivatives
Petina OA, et al.
Synthesis, 45(06), 803-809 (2013)
Mechanistic Pathway for the Formation of Radial Polystyrenes Using Diacyl Chloride
Kumar S, et al.
Macromolecules, 45(6), 2675-2681 (2012)
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