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About This Item
Linear Formula:
CH3OCH2COCl
CAS Number:
Molecular Weight:
108.52
Beilstein/REAXYS Number:
1740244
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
assay
97%
form
liquid
refractive index
n20/D 1.419 (lit.)
bp
112-113 °C (lit.)
density
1.187 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
COCC(Cl)=O
InChI
1S/C3H5ClO2/c1-6-2-3(4)5/h2H2,1H3
InChI key
JJKWHOSQTYYFAE-UHFFFAOYSA-N
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Application
Methoxyacetyl chloride can be used for methoxyacetylation of:
It can also be used for the synthesis of β-lactams by reacting with imines. and in the post-synthetic modification of the metal-organic framework (MOF), MIL-101, to synthesize a catalyst for cycloaddition reaction of CO2 with propylene oxide.
- Bilocularin A to synthesize 8-Methoxyacetoxybilocularin A.
- Substituted and unsubstituted benzamides to synthesize N-(2-methoxyacetyl)-benzamides.
It can also be used for the synthesis of β-lactams by reacting with imines. and in the post-synthetic modification of the metal-organic framework (MOF), MIL-101, to synthesize a catalyst for cycloaddition reaction of CO2 with propylene oxide.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk_germany
WGK 3
flash_point_f
82.4 °F
flash_point_c
28 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Synthesis of Quinolinone Alkaloids via Aryne Insertions into Unsymmetric Imides in Flow.
Schwan J, et al.
Organic Letters, 20(23), 7661?7664-7661?7664 (2018)
Bioactive dihydro-?-agarofuran sesquiterpenoids from the Australian rainforest plant Maytenus bilocularis.
Wibowo M, et al.
Journal of Natural Products, 79(5), 1445-1453 (2016)
An investigation towards the diastereoselective synthesis of 3-acetoxy/methoxy/phthalimido-β-lactams using chiral imines.
Bhalla A, et al.
Tetrahedron Asymmetry, 28(2), 307-316 (2017)
Radu A Gropeanu et al.
PloS one, 7(9), e43657-e43657 (2012-09-13)
Three different variants of photoactivatable caged paclitaxel (PTX) have been synthesized and their bioactivity was characterized in in vitro assays and in living cells. The caged PTXs contain the photoremovable chromophore 4,5-dimethoxy-2-nitrobenzyloxycarbonyl (Nvoc) attached to position C7, C2' and to
Functionalized MIL-101 with imidazolium-based ionic liquids for the cycloaddition of CO2 and epoxides under mild condition.
Liu D, et al.
Applied Surface Science, 428(45), 218-225 (2018)
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