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226122

2-Bromomethyl-1,3-dioxolane

Name: 2-Bromomethyl-1,3-dioxolane
Brand: ALDRICH

96%

Synonym(s):

Bromoacetaldehyde ethylene acetal

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About This Item

Empirical Formula (Hill Notation):

C₄H₇BrO₂

CAS Number:

4360-63-8

Molecular Weight:

167.00

Beilstein/REAXYS Number:

103309

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24853544

EC Number:

224-443-6

MDL number:

MFCD00003214

Assay:

96%

Form:

liquid

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Properties

Quality Level

200

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

Description

Application

2-Bromomethyl-1,3-dioxolane was used in the synthesis of 1,4-benzoxazepine (BZO) compounds.

pictograms

GHS07

signalword

Warning

hcodes

H315,H319

pcodes

P264 - P280 - P302 + P352 - P305 + P351 + P338 - P332 + P313 - P337 + P313

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

143.6 °F - closed cup

flash_point_c

62 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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New 5-HT1A receptor agonists possessing 1,4-benzoxazepine scaffold exhibit highly potent anti-ischemic effects.

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

Global Trade Item Number

SKU	GTIN
226122-25G	04061838780034
226122-100G	04061838780027