2-Chloro-1,3,2-dioxaphospholane 2-oxide - CAS 6609-64-9

Catalog:	BB032913
Product Name:	2-Chloro-1,3,2-dioxaphospholane 2-oxide
CAS:	6609-64-9
Synonyms:	2-chloro-1,3,2lambda5-dioxaphospholane 2-oxide

Technical Data

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Computed Properties

IUPAC Name:	2-chloro-1,3,2λ5-dioxaphospholane 2-oxide
Description:	2-Chloro-1,3,2-dioxaphospholane 2-oxide (CAS# 6609-64-9) is used in the synthesis of α-naphthylphosphorylcholine as a method to detect phospholipase C activity.
Molecular Weight:	142.48
Molecular Formula:	C2H4ClO3P
Canonical SMILES:	C1COP(=O)(O1)Cl
InChI:	InChI=1S/C2H4ClO3P/c3-7(4)5-1-2-6-7/h1-2H2
InChI Key:	SBMUNILHNJLMBF-UHFFFAOYSA-N
Boiling Point:	89-91 °C / 0.8 mmHg (lit.)
Density:	1.55 g/cm³
Appearance:	Yellow to brown liquid
MDL:	MFCD00043138
LogP:	1.38010

Publication Number	Title	Priority Date
CN-113197690-A	Dental implant with hydrophilic antibacterial property	20210510
CN-112225756-A	Preparation method of cyclic chlorophosphate	20201217
CN-112225756-B	Preparation method of cyclic chlorophosphate	20201217
CN-112239543-A	Cross-linked comb-shaped polymer electrolyte, and preparation method and application thereof	20201019
CN-112142986-A	Functionalized diblock copolymer and preparation method and application thereof	20200925

PMID	Publication Date	Title	Journal
15818585	20050419	Novel acrylonitrile-based copolymers containing phospholipid moieties: synthesis and characterization	Macromolecular bioscience
15779969	20050329	Surface modification of polyacrylonitrile-based membranes by chemical reactions to generate phospholipid moieties	Langmuir : the ACS journal of surfaces and colloids
12036012	20020501	Synthetic studies on glycosphingolipids from protostomia phyla: synthesis of amphoteric glycolipid analogues from the porcine nematode, Ascaris suum	Chemical & pharmaceutical bulletin
11724239	20011101	Synthetic studies on glycosphingolipids from Protostomia phyla: synthesis of amphoteric glycolipid analogues containing a phosphocholine residue from the earthworm Pheretima hilgendorfi	Chemical & pharmaceutical bulletin

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Related Functional Groups

Phosphorus Compounds

[4671-77-6]
1,4-Butanediphosphonic acid
[115826-95-4]
Dichloro[(R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]palladium(II)
[39600-44-7]
Glycine,N-(phosphonomethyl)-, 1-methyl ester
[2404-75-3]
Diethyl n-butanephosphonate
[35051-50-4]
Ethyl 2-(diethoxyphosphoryl)-3-methylbutanoate
[61341-12-6]
Ethyl 2-acetamido-3-diethoxyphosphorylpropanoate

GHS Hazard Statement:	H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
Precautionary Statement:	P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501
Signal Word:	Danger

Complexity:	104
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	141.9586587
Formal Charge:	0
Heavy Atom Count:	7
Hydrogen Bond Acceptor Count:	3
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	141.9586587
Rotatable Bond Count:	0
Topological Polar Surface Area:	35.5 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	0