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
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
form
solid
mp
128-132 °C (lit.)
SMILES string
[H]C(=O)c1cc2OCOc2cc1Br
InChI
1S/C8H5BrO3/c9-6-2-8-7(11-4-12-8)1-5(6)3-10/h1-3H,4H2
InChI key
CSQUXTSIDQURDV-UHFFFAOYSA-N
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 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)
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?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)
"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)
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