Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

155578

Sigma-Aldrich

6-Bromoveratraldehyde

98%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
BrC6H2-3,4-(OCH3)2CHO
CAS Number:
5392-10-9
Molecular Weight:
245.07
EC Number:
226-390-4
MDL number:
MFCD00003301
UNSPSC Code:
12352100
PubChem Substance ID:
24849544
NACRES:
NA.22

Assay

98%

form

powder

mp

150-151 °C (lit.)

functional group

aldehyde
bromo

SMILES string

COc1cc(Br)c(C=O)cc1OC

InChI

1S/C9H9BrO3/c1-12-8-3-6(5-11)7(10)4-9(8)13-2/h3-5H,1-2H3

InChI key

UQQROBHFUDBOOK-UHFFFAOYSA-N

Application

6-Bromoveratraldehyde was used in the preparation of benzylchromenylamines.

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBC8791V
STBB1703V
STBB1703
S15180
10631KD

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

J Razafimbelo et al.
Chemical & pharmaceutical bulletin, 46(1), 34-41 (1998-02-20)
Condensation of 5-amino, 6-amino, 7-amino and 8-amino-2,2-dimethyl-2H-chromenes with either 6-bromoveratraldehyde or 6-chloropiperonal afforded the corresponding Schiff bases, which were subsequently reduced to the corresponding benzylchromenylamines 30-33 and 36-39. Lithium diisopropylamide-mediated cyclization of those amines, followed by spontaneous air oxidation, afforded

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service