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Merck
CN

519766

Sigma-Aldrich

Cartridge for Phosgene Generation

0.05 mole

Synonym(s):

Triphosgene, Cartridge for Phosgene Generation

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About This Item

Empirical Formula (Hill Notation):
C3Cl6O3
CAS Number:
Molecular Weight:
296.75
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:
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SMILES string

ClC(Cl)=O

InChI

1S/C3Cl6O3/c4-2(5,6)11-1(10)12-3(7,8)9

InChI key

UCPYLLCMEDAXFR-UHFFFAOYSA-N

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Yu Zhang et al.
Colloids and surfaces. B, Biointerfaces, 122, 368-374 (2014-08-03)
In this work, the block copolypeptide surfactant, poly(l-lysine·HBr)40-b-poly(racemic-leucine)20, was synthesized and characterized, then used to build water-in-oil-in-water (W/O/W) double emulsions. Double emulsions are usually prepared by a two-step emulsification process and commonly stabilized using a combination of hydrophilic and hydrophobic
Hailiang Wu et al.
Journal of controlled release : official journal of the Controlled Release Society, 189, 1-10 (2014-06-24)
Nanocarriers have been used for specific delivery of therapeutic agents to solid tumors based on the enhanced permeability and retention in cancerous tissues. Despite metastasis is the main reason of cancer-related death and a priority for nanocarrier-based therapies, the targeting
Horacio Cabral et al.
ACS nano, 9(5), 4957-4967 (2015-04-17)
Occult nodal metastases increase the risk of cancer recurrence, demoting prognosis and quality of life of patients. While targeted drug delivery by using systemically administered nanocarriers can potentially control metastatic disease, lymph node metastases have been mainly dealt by locally
Jianqin Lu et al.
Biomaterials, 62, 176-187 (2015-06-10)
Camptothecin (CPT) is a potent antitumor agent and functions via inhibiting the activity of topoisomerase I during DNA replication. However, the clinical application of CPT has been greatly hindered by its extremely poor solubility, the instability of its active lactone
K Pavić et al.
European journal of medicinal chemistry, 86, 502-514 (2014-09-10)
Novel primaquine semicarbazides 7a-l and ureas 9a-g with modified benzhydryl, trityl, phenyl or hydroxyalkyl substituents were prepared and evaluated for cytostatic and antioxidative activities. Two synthetic approaches for preparation of the title semicarbazides were applied, both having certain advantages. In

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