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Merck
CN

149209

Methyl methoxyacetate

99%

Synonym(s):

Methoxyacetic acid methyl ester, Methyl α-methoxyacetate, Methyl 2-methoxyacetate

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About This Item

Linear Formula:
CH3OCH2COOCH3
CAS Number:
6290-49-9
Molecular Weight:
104.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848936
EC Number:
228-539-9
Beilstein/REAXYS Number:
1742944
MDL number:
MFCD00008451
Assay:
99%
Form:
liquid

Key Documents

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InChI key

QRMHDGWGLNLHMN-UHFFFAOYSA-N

InChI

1S/C4H8O3/c1-6-3-4(5)7-2/h3H2,1-2H3

SMILES string

COCC(=O)OC

assay

99%

form

liquid

refractive index

n20/D 1.396 (lit.)

bp

129-130 °C (lit.)

density

1.051 g/mL at 25 °C (lit.)

functional group

ester, ether

Quality Level

100

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Application

Methyl methoxyacetate was used in the preparation of 4-hydroxy-2-mercapto-5-methoxypyrimidine (II).

pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

flash_point_f

95.0 °F - closed cup

flash_point_c

35 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
STBL2384
STBK0055
STBJ5639
STBH4609
STBG4826V

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Shigehiro Namiki et al.
The International journal of neuroscience, 119(2), 214-226 (2009-01-07)
Loading neurons with membrane permeable Ca2+ indicators is a core experimental procedure in functional multineuron Ca2+ imaging (fMCI), an optical technique for monitoring multiple neuronal activities. Although fMCI has been applied to several brain networks, including cerebral cortex, hippocampus, and
888. Pyrimidines. Part XI. Synthesis of 5-hydroxypyrimidine and related compounds.
Chesterfield JH, et al.
Journal of the Chemical Society, 4590-4596 (1960)
[Information from the Soviet Toxicology Center].
Farmakologiia i toksikologiia, 43(6), 750-751 (1980-11-01)
K Thompson et al.
Biotechnic & histochemistry : official publication of the Biological Stain Commission, 87(7), 468-483 (2012-09-19)
Stimulated by difficulties experienced when using fluo-3 AM, we developed a general mechanistic model to aid understanding and practical application of calcium probes applied as acetoxymethyl (AM) esters. Several practical issues previously overlooked or under-emphasized are considered by this model.

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