Diglycolyl chloride

Product Information

Molecular Formula:
C4H4Cl2O3
Molecular Weight:
170.98
Description
Diglycolyl chloride (CAS# 21062-20-4) is a useful research chemical.
Synonyms
2-(2-chloro-2-oxoethoxy)acetyl chloride
IUPAC Name
2-(2-chloro-2-oxoethoxy)acetyl chloride
Canonical SMILES
C(C(=O)Cl)OCC(=O)Cl
InChI
InChI=1S/C4H4Cl2O3/c5-3(7)1-9-2-4(6)8/h1-2H2
InChI Key
GTZXSBQCNBNWPK-UHFFFAOYSA-N
Boiling Point
84-87 ℃2 mmHg (lit.)
Melting Point
121-123 ℃
Flash Point
>230 °F
Purity
> 97.0 % (GC) (T)
Density
1.439 g/mL at 25 ℃ (lit.)
Appearance
Colorless to dark yellow liquid
Refractive Index
n20/D 1.473(lit.)
LogP
0.53380

Safety Information

Hazards
H290:
May be corrosive to metals.
H314:
Causes severe skin burns and eye damage.
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

Computed Properties

XLogP3
1.2
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
4
Exact Mass
169.9537494 g/mol
Monoisotopic Mass
169.9537494 g/mol
Topological Polar Surface Area
43.4Ų
Heavy Atom Count
9
Formal Charge
0
Complexity
109
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
WO-2022047268-A1 Deposition of films onto battery material powders 2020-08-29
US-2022002229-A1 Diglycolamide derivatives for separation and recovery of rare earth elements from aqueous solutions 2020-07-06
US-2022002840-A1 Methods for separation and recovery of rare earth elements from aqueous solutions using diglycolamide derivatives 2020-07-06
WO-2022010758-A1 Diglycolamide derivatives for separation and recovery of rare earth elements from aqueous solutions 2020-07-06
WO-2022010759-A2 Methods for separation and recovery of rare earth elements from aqueous solutions using diglycolamide derivatives 2020-07-06
WO-2021254931-A1 Polyamide microcapsules 2020-06-16
KR-20210116860-A Abtamer-based particles and method for manufacturing the same 2020-03-18
KR-20210116861-A Aptamer-based particles and method for manufacturing the same 2020-03-18
KR-20210116339-A Particles encapsulated in a targeted aptamer conjugate and its use 2020-03-16
WO-2021187851-A1 Particles encapsulating targeted aptamer conjugates, and use thereof 2020-03-16

Literatures

PMID Publication Date Title Journal
21583610 2009-07-18 1,15:21,35-Bis(oxydiethyl-ene)-5,8,11,18,25,28,31,38-octa-oxa-1,15,21,35-tetra-azacyclo-tetra-decane-16,20,36,40-tetra-one-benzene (1/2): a macrotricyclic tetra-lactam Acta crystallographica. Section E, Structure reports online
21201201 2008-09-24 6,7,9,10-Tetra-hydro-16,22-ethano-oxyethano-5,8,11,19-tetra-oxa-16,22-diaza-dibenzo[h,q]cyclo-octa-decine-17,21-dione: a benzyl-annelated macrobicyclic diamide 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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