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258601

Sigma-Aldrich

Vanillin acetate

98%

Synonym(s):

4-Formyl-2-methoxyphenyl acetate

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About This Item

Linear Formula:
CH3CO2C6H3-4-(CHO)-2-OCH3
CAS Number:
Molecular Weight:
194.18
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

solid

mp

77-79 °C (lit.)

SMILES string

COc1cc(C=O)ccc1OC(C)=O

InChI

1S/C10H10O4/c1-7(12)14-9-4-3-8(6-11)5-10(9)13-2/h3-6H,1-2H3

InChI key

PZSJOBKRSVRODF-UHFFFAOYSA-N

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General description

Chemoselective reduction of vanillin acetate using sodium borohydride has been reported.

Application

Vanillin acetate has been used in preparation of:
  • 2-nitrohomovanillic acid
  • 2-nitrovanildin acetate
  • 2-nitro-3,4-duimethoxybenzaldehyde

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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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The discovery-oriented approach to organic chemistry. 6. Selective reduction in organic chemistry: Reduction of aldehydes in the presence of esters using sodium borohydride.
Baru AR and Mohan RS
Journal of Chemical Education, 82(11), 1674-1674 (2005)
Azlactones and phenylacetic acids derived from the 2-nitro-derivatives of vanillin, isovanillin, and veratraldehyde.
S F MacDONALD
Journal of the Chemical Society, 174, 376-378 (1948-03-01)

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