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454796

Sigma-Aldrich

Benzyloxyacetaldehyde diethyl acetal

95%

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About This Item

Linear Formula:
C6H5CH2OCH2CH(OC2H5)2
CAS Number:
42783-78-8
Molecular Weight:
224.30
MDL number:
MFCD00051786
UNSPSC Code:
12352100
PubChem Substance ID:
24868971
NACRES:
NA.22

assay

95%

refractive index

n20/D 1.478 (lit.)

bp

99-100 °C/0.6 mmHg (lit.)

density

0.987 g/mL at 25 °C (lit.)

SMILES string

CCOC(COCc1ccccc1)OCC

InChI

1S/C13H20O3/c1-3-15-13(16-4-2)11-14-10-12-8-6-5-7-9-12/h5-9,13H,3-4,10-11H2,1-2H3

InChI key

VTYTZCJKJNWMGA-UHFFFAOYSA-N

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

174.2 °F - closed cup

flash_point_c

79 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

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Synthesis of novel 1, 3-dioxolane nucleoside analogues.
Cai D-M, et al.
Chin. J. Chem., 22(12), 1425-1431 (2004)
(?)-Dioxolane-T ((?)-1-[(2?, 4?)-2-(hydroxymethyl)-4-dioxolanyl] thymine): A new 2', 3'-dideoxynucleoside prototype within vitro activity against HIV.
Norbeck DW, et al.
Tetrahedron Letters, 30(46), 6263-6266 (1989)
Silas P Cook et al.
The Journal of biological chemistry, 277(31), 27782-27792 (2002-05-22)
Serine racemase (SR) is a brain enzyme present in glial cells, where it isomerizes L-serine into D-serine that, in turn, diffuses and coactivates the N-methyl-D-aspartate receptor through the binding to the so-called "glycine site." We have developed a method for

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