226122
2-Bromomethyl-1,3-dioxolane
96%
Synonym(s):
Bromoacetaldehyde ethylene acetal
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₹3,756.28
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₹10,554.38
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25 G
₹3,756.28
100 G
₹10,554.38
About This Item
Empirical Formula (Hill Notation):
C4H7BrO2
CAS Number:
Molecular Weight:
167.00
Beilstein:
103309
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
96%
form
liquid
refractive index
n20/D 1.482 (lit.)
bp
80-82 °C/27 mmHg (lit.)
density
1.613 g/mL at 25 °C (lit.)
functional group
bromo
ether
SMILES string
BrCC1OCCO1
InChI
1S/C4H7BrO2/c5-3-4-6-1-2-7-4/h4H,1-3H2
InChI key
CKIIJIDEWWXQEA-UHFFFAOYSA-N
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Application
2-Bromomethyl-1,3-dioxolane was used in the synthesis of 1,4-benzoxazepine (BZO) compounds[1].
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
143.6 °F - closed cup
Flash Point(C)
62 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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K Kamei et al.
Bioorganic & medicinal chemistry letters, 11(4), 595-598 (2001-03-07)
A series of new 3-substituted-4-(4-aminobutyl)-1,4-benzoxazepin-5(4H)-one derivatives (1-5) which showed a very high affinity for 5-HT1A receptor with good selectivity over dopamine D2 receptor was synthesized. Among these compounds, 3-chloro-4-[4-[4-(2-pyridinyl)-1,2,3,6-tetrahydropyridin-1-yl]butyl]-1,4-benzoxazepin-5(4H)-one (5: SUN N4057) exhibited remarkable neuroprotective activity in a transient middle
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