Home Aldehydes Benzyloxyacetaldehyde

Benzyloxyacetaldehyde

CAS No.:
60656-87-3
Catalog Number:
AG0035YM
Molecular Formula:
C9H10O2
Molecular Weight:
150.1745
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$161
- +
25g
95%
In Stock USA
United States
$561
- +
Product Description
Catalog Number:
AG0035YM
Chemical Name:
Benzyloxyacetaldehyde
CAS Number:
60656-87-3
Molecular Formula:
C9H10O2
Molecular Weight:
150.1745
MDL Number:
MFCD00191779
IUPAC Name:
2-phenylmethoxyacetaldehyde
InChI:
InChI=1S/C9H10O2/c10-6-7-11-8-9-4-2-1-3-5-9/h1-6H,7-8H2
InChI Key:
NFNOAHXEQXMCGT-UHFFFAOYSA-N
SMILES:
O=CCOCc1ccccc1
EC Number:
262-349-7
Properties
Complexity:
106  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
150.068g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
150.177g/mol
Monoisotopic Mass:
150.068g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
26.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.1  
Literature
Title Journal
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Generating a generation of proteasome inhibitors: from microbial fermentation to total synthesis of salinosporamide a (marizomib) and other salinosporamides. Marine drugs 20100101
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Serine hydroxymethyl transferase from Streptococcus thermophilus and L-threonine aldolase from Escherichia coli as stereocomplementary biocatalysts for the synthesis of beta-hydroxy-alpha,omega-diamino acid derivatives. Chemistry (Weinheim an der Bergstrasse, Germany) 20080101
Single diastereomers of polyhydroxylated 9-oxa-1-azabicyclo[4.2.1]nonanes from intramolecular 1,3-dipolar cycloaddition of omega-unsaturated nitrones. The Journal of organic chemistry 20061027
Recombinant production of serine hydroxymethyl transferase from Streptococcus thermophilus and its preliminary evaluation as a biocatalyst. Applied microbiology and biotechnology 20050901
(R)-Goniothalamin: total syntheses and cytotoxic activity against cancer cell lines. Bioorganic & medicinal chemistry 20050415
Crystal structure of vinorine synthase, the first representative of the BAHD superfamily. The Journal of biological chemistry 20050408
Aldol additions of dihydroxyacetone phosphate to N-Cbz-amino aldehydes catalyzed by L-fuculose-1-phosphate aldolase in emulsion systems: inversion of stereoselectivity as a function of the acceptor aldehyde. Chemistry (Weinheim an der Bergstrasse, Germany) 20050218
Chiral 2,6-bis(oxazolinyl)pyridine-rare earth metal complexes as catalysts for highly enantioselective 1,3-dipolar cycloaddition reactions of 2-benzopyrylium-4-olates. The Journal of organic chemistry 20050107
An intramolecular 1,3-dipolar cycloaddition reaction towards the synthesis of chiral azetidine nucleoside analogues: the D-gluco case. Nucleosides, nucleotides & nucleic acids 20050101
Stereo- and regioselectivity of Pd(0)/InI-mediated allylic additions to aldehydes and ketones. In situ generation of allylindium(III) intermediates from N-acylnitroso Diels-Alder cycloadducts and 1-amino-4-acetoxycyclopentenes. The Journal of organic chemistry 20030110
Highly enantioselective 1,3-dipolar cycloaddition reactions of 2-benzopyrylium-4-olate catalyzed by chiral Lewis acids. Journal of the American Chemical Society 20021218
Properties