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Merck
CN

161756

Bromomethyl methyl ether

technical grade, 90%

Synonym(s):

1-Bromomethyl methyl ether, Bromomethoxymethane, Methoxymethyl bromide

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About This Item

Linear Formula:
BrCH2OCH3
CAS Number:
13057-17-5
Molecular Weight:
124.96
NACRES:
NA.22
PubChem Substance ID:
24849953
UNSPSC Code:
12352100
MDL number:
MFCD00000171

Key Documents

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Product Name

Bromomethyl methyl ether, technical grade, 90%

InChI

1S/C2H5BrO/c1-4-2-3/h2H2,1H3

SMILES string

COCBr

InChI key

JAMFGQBENKSWOF-UHFFFAOYSA-N

grade

technical grade

assay

90%

form

liquid

refractive index

n20/D 1.456 (lit.)

bp

87 °C (lit.)

density

1.531 g/mL at 25 °C (lit.)

functional group

bromo
ether

storage temp.

2-8°C

Quality Level

100

Related Categories

Application

Bromomethyl methyl ether was used in enantiocontrolled synthesis of intermediate containing carbons 18 to 35 of the macrocyclic immunosuppressant FK-506. It was used in the synthesis of 1-methoxymethyl-4-tritylthio-2-azetidinone.

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Warning

Hazard Classifications

Acute Tox. 4 Dermal - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

80.6 °F - closed cup

flash_point_c

27 °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
MKCZ6240
MKCX3411
MKCW2544
MKCR9212
MKCR0221

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Nuclear analogs of β-lactam antibiotics. XVI. Aldol condensations of N-protected 4-tritylthio-2-azetidinones.
Martel A, et al.
Canadian Journal of Chemistry, 61(3), 613-618 (1983)
Enantioselective synthesis of the C (18)-C (35) segment of immunosuppressant FK-506 using efficient new methodology.
Corey EJ and Huang H-C.
Tetrahedron Letters, 30(39), 5235-5238 (1989)
Archana Prasad et al.
Scientific reports, 6, 39490-39490 (2016-12-22)
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease associated with aggregation of TAR DNA-binding protein-43 (TDP-43) in neuronal cells and manifests as motor neuron dysfunction &muscle atrophy. The carboxyl-terminal prion-like domain of TDP-43 can aggregate in vitro into toxic

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