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Merck
CN

137685

2-Bromoethyl acetate

97%

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About This Item

Linear Formula:
CH3COOCH2CH2Br
CAS Number:
Molecular Weight:
167.00
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-159-8
Beilstein/REAXYS Number:
1743110
MDL number:
Assay:
97%
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InChI

1S/C4H7BrO2/c1-4(6)7-3-2-5/h2-3H2,1H3

InChI key

RGHQKFQZGLKBCF-UHFFFAOYSA-N

SMILES string

CC(=O)OCCBr

assay

97%

impurities

<3% acetic anhydride

bp

159 °C (lit.)

mp

−14-−13.8 °C (lit.)

density

1.514 g/mL at 25 °C (lit.)

functional group

bromo, ester

Application

2-Bromoethyl acetate was used as alkylating reagent during asymmetric total synthesis of (+)-1-deoxylycorine and (+)-lycorine.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

159.8 °F - closed cup

flash_point_c

71 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Takuya Uto et al.
Physical chemistry chemical physics : PCCP, 20(31), 20669-20677 (2018-07-31)
Chitin is a promising biomass resource and has high potential for industrial applications owing to its huge annual production in nature. However, it exhibits poor processability and solubility due to its very stable and crystalline character. Recently, ionic liquids (ILs)
The first asymmetric total syntheses of (+)-lycorine and (+)-1-deoxylycorine.
Schultz AG, et al.
Journal of the American Chemical Society, 118(26), 6210-6219 (1996)

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