Home Aldehydes 60656-87-3
60656-87-3,MFCD00191779
Catalog No.:AA0035VU

60656-87-3 | Benzyloxyacetaldehyde

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1g
95%
in stock  
$24.00   $17.00
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5g
95%
in stock  
$80.00   $56.00
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10g
95%
in stock  
$143.00   $100.00
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25g
95% (stabilized with 0.5%Catechol)
in stock  
$218.00   $153.00
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100g
95% (stabilized with 0.5%Catechol)
in stock  
$768.00   $538.00
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  • Technical Information
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  • Technical Information
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Technical Information
Catalog Number:
AA0035VU
Chemical Name:
Benzyloxyacetaldehyde
CAS Number:
60656-87-3
Molecular Formula:
C9H10O2
Molecular Weight:
150.1745
MDL Number:
MFCD00191779
SMILES:
O=CCOCc1ccccc1
Properties
Properties
 
BP:
118-120°C at 760 mmHg  
Form:
Liquid  
Refractive Index:
n20/D 1.518(lit.)  
Storage:
Inert atmosphere;-20 ℃;  

Computed Properties
 
Complexity:
106  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
4  
XLogP3:
1.1  

Literature

Title: Catalysis through temporary intramolecularity: mechanistic investigations on aldehyde-catalyzed Cope-type hydroamination lead to the discovery of a more efficient tethering catalyst.

Journal: Journal of the American Chemical Society 20121010

Title: Generating a generation of proteasome inhibitors: from microbial fermentation to total synthesis of salinosporamide a (marizomib) and other salinosporamides.

Journal: Marine drugs 20100101

Title: Synthetic studies on (-)-lemonomycin: an efficient asymmetric synthesis of lemonomycinone amide.

Journal: The Journal of organic chemistry 20090306

Title: D-fructose-6-phosphate aldolase in organic synthesis: cascade chemical-enzymatic preparation of sugar-related polyhydroxylated compounds.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20090101

Title: 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.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20080101

Title: Single diastereomers of polyhydroxylated 9-oxa-1-azabicyclo[4.2.1]nonanes from intramolecular 1,3-dipolar cycloaddition of omega-unsaturated nitrones.

Journal: The Journal of organic chemistry 20061027

Title: Recombinant production of serine hydroxymethyl transferase from Streptococcus thermophilus and its preliminary evaluation as a biocatalyst.

Journal: Applied microbiology and biotechnology 20050901

Title: (R)-Goniothalamin: total syntheses and cytotoxic activity against cancer cell lines.

Journal: Bioorganic & medicinal chemistry 20050415

Title: Crystal structure of vinorine synthase, the first representative of the BAHD superfamily.

Journal: The Journal of biological chemistry 20050408

Title: 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.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20050218

Title: 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.

Journal: The Journal of organic chemistry 20050107

Title: An intramolecular 1,3-dipolar cycloaddition reaction towards the synthesis of chiral azetidine nucleoside analogues: the D-gluco case.

Journal: Nucleosides, nucleotides & nucleic acids 20050101

Title: 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.

Journal: The Journal of organic chemistry 20030110

Title: Highly enantioselective 1,3-dipolar cycloaddition reactions of 2-benzopyrylium-4-olate catalyzed by chiral Lewis acids.

Journal: Journal of the American Chemical Society 20021218

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