563013
6-Bromo-1,3-benzodioxole-5-carboxaldehyde
97%
Synonym(s):
6-Bromopiperonal
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About This Item
Linear Formula:
C6H2BrCHOCH2O2
CAS Number:
Molecular Weight:
229.03
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
InChI
1S/C8H5BrO3/c9-6-2-8-7(11-4-12-8)1-5(6)3-10/h1-3H,4H2
SMILES string
[H]C(=O)c1cc2OCOc2cc1Br
InChI key
CSQUXTSIDQURDV-UHFFFAOYSA-N
assay
97%
form
solid
mp
128-132 °C (lit.)
functional group
aldehyde, bromo
Quality Level
General description
6-Bromo-1,3-benzodioxole-5-carboxaldehyde can be synthesized by subjecting, 1,3-benzodioxole-5-carboxaldehyde to bromination.
Application
6-Bromo-1,3-benzodioxole-5-carboxaldehyde may be used to synthesize, 2H-indazoles and 2-allyl-N-[(6-bromobenzo[d][1,3]dioxol-5-yl)methyl]aniline
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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"Synthesis of Substituted Tetrahydroindoloisoquinoline Derivatives via
Intramolecular Pd-Catalyzed Alkene Carboamination Reactions"
Intramolecular Pd-Catalyzed Alkene Carboamination Reactions"
Alicea J and Wolfe PJ
The Journal of Organic Chemistry, 79(9), 4212-4217 (2014)
?Facile derivatization of 1, 3-benzodioxole-5-carboxaldehyde and their
antimicrobial activities?
antimicrobial activities?
Ogunjobi KJ and Lajide L et al.
Journal of Natural Products and Biomedical Research, 1(2) (2015)
"Consecutive Condensation, C?N and N?N Bond Formations: A Copper-Catalyzed One-Pot Three-Component Synthesis of 2 H-Indazole"
Kumar RM, et al.
Organic Letters, 13(13), 3542- 3545 (2011)
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