DIMETHYLMALONYL CHLORIDE

Product Information

Molecular Formula:
C5H6Cl2O2
Molecular Weight:
169.01
Description
DIMETHYLMALONYL CHLORIDE stands as an indispensable mediatory entity involved in the intricate amalgamation of diverse pharmaceuticals. Its utilization primarily encompasses the fabrication of potent antiviral and antimicrobial agents, alongside profound contributions to the expedient synthesis of anticancer medication. Psuedomorphic in nature, this multi-faceted compound assumes a pivotal position in the therapeutic intervention of infectious viral and bacterial maladies, as well as malignant neoplastic pathologies, thus propelling its esteemed significance within the domain of biomedicinal prowess.
Synonyms
DIMETHYLMALONYL CHLORIDE; DIMETHYLMALONYL DICHLORIDE
IUPAC Name
2,2-dimethylpropanedioyl dichloride
Canonical SMILES
CC(C)(C(=O)Cl)C(=O)Cl
InChI
InChI=1S/C5H6Cl2O2/c1-5(2,3(6)8)4(7)9/h1-2H3
InChI Key
CJXQAYQWVNXIQE-UHFFFAOYSA-N
Boiling Point
60 °C/10 mmHg (lit.)
Flash Point
123.8 °CF - closed cup
Purity
0.98
Density
1.278
Refractive Index
n20/D 1.451 (lit.)

Safety Information

Hazards
H226 - H314
Precautionary Statement
P280 - P305 + P351 + P338 - P310

Computed Properties

XLogP3
2.4
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
2
Exact Mass
167.9744848 g/mol
Monoisotopic Mass
167.9744848 g/mol
Topological Polar Surface Area
34.1Ų
Heavy Atom Count
9
Formal Charge
0
Complexity
135
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-112500273-A Preparation method of light stabilizer 2, 2-dibenzoyl propane 2020-12-03
US-2022048879-A1 Synthesis of small molecules inspired by Phomoxanthone A 2020-08-13
WO-2022036040-A1 Synthesis of small molecules inspired by phomoxanthone a 2020-08-13
CN-111606868-A Preparation method of bidentate oxazoline chiral ligand 2020-06-23
JP-2021195539-A Thermosetting resin composition 2020-06-12
JP-2021195537-A Adhesives, aqueous dispersions and resin modifiers containing modified polyolefins and modified polyolefins 2020-06-10
WO-2021101606-A1 Compositions for sunscreen compounds and methods thereof 2019-11-18
CN-110724112-A Bisoxazoline ligand compound and synthetic method thereof 2019-06-28
JP-2020128368-A Medicine containing an azole-substituted pyridine compound as an active ingredient 2019-02-08
WO-2020069023-A1 High-temperature polymer aerogel composites 2018-09-25

Literatures

PMID Publication Date Title Journal
21589344 2010-11-27 {2,2-Bis[(4S)-4-isopropyl-4,5-dihydro-1,3-oxazol-2-yl]propane}-bis-(N,N-dimethyl-formamide)-copper(II) bis-[hexa-fluoridoanti-monate(V)] Acta crystallographica. Section E, Structure reports online
21587514 2010-09-08 2,2'-(Propane-2,2-di-yl)dibenzothia-zole Acta crystallographica. Section E, Structure reports online
19842700 2009-11-11 An N,N'-diamidocarbene: studies in C-H insertion, reversible carbonylation, and transition-metal coordination chemistry Journal of the American Chemical Society
21582678 2009-06-06 {2,2-Bis[(4S)-4-tert-butyl-4,5-dihydro-1,3-oxazol-2-yl]propane}bis-(N,N-di-methyl-formamide)copper(II) bis-(hexa-fluoridoantimonate) Acta crystallographica. Section E, Structure reports online
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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