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123986

Sigma-Aldrich

Bromoacetaldehyde diethyl acetal

97%

Synonym(s):

2-Bromo-1,1-diethoxyethane, Bromoacetal

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About This Item

Linear Formula:
BrCH2CH(OC2H5)2
CAS Number:
2032-35-1
Molecular Weight:
197.07
Beilstein:
635754
EC Number:
217-989-1
MDL number:
MFCD00000214
UNSPSC Code:
12352100
PubChem Substance ID:
24847591
NACRES:
NA.22

Assay

97%

form

liquid

refractive index

n20/D 1.439 (lit.)

bp

66-67 °C/18 mmHg (lit.)

density

1.31 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CCOC(CBr)OCC

InChI

1S/C6H13BrO2/c1-3-8-6(5-7)9-4-2/h6H,3-5H2,1-2H3

InChI key

LILXDMFJXYAKMK-UHFFFAOYSA-N

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General description

Bromoacetaldehyde diethyl acetal reacts with anhydrous trimethylamine to form glycine betaine aldehyde. It reacts with different thiophenols in the presence of KOH/Cu to produce the corresponding ketone and diethyl acetals.
May darken in storage

Application

Bromoacetaldehyde diethyl acetal has been used in the synthesis of monomer 2-(2,2-dimethoxy)ethoxyethyl vinyl ether. It has been used as synthetic building block.

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301,H315,H319,H330

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

149.0 °F - closed cup

Flash Point(C)

65 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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A novel series of thiosemicarbazone and aminoacyl-thiazolidones derivatives were synthesized. Their structure suggests that these compounds could have anti-Trypanosoma cruzi activity. Biological evaluation indicates that some of these compounds are able to inhibit the growth of T. cruzi in concentrations
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Synthesis of graft copolymers based on selective living cationic polymerization using an acetal group with a combination of Lewis acids.
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