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563013

6-Bromo-1,3-benzodioxole-5-carboxaldehyde

Name: 6-Bromo-1,3-benzodioxole-5-carboxaldehyde
Brand: ALDRICH

97%

Synonym(s):

6-Bromopiperonal

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About This Item

Linear Formula:

C₆H₂BrCHOCH₂O₂

CAS Number:

15930-53-7

Molecular Weight:

229.03

NACRES:

NA.22

PubChem Substance ID:

24880069

UNSPSC Code:

12352100

MDL number:

MFCD00022952

Assay:

97%

Form:

solid

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Properties

Quality Level

100

assay

97%

form

solid

mp

128-132 °C (lit.)

functional group

aldehyde, bromo

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

Description

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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?Facile derivatization of 1, 3-benzodioxole-5-carboxaldehyde and their
antimicrobial activities?

Ogunjobi KJ and Lajide L et al.

Journal of Natural Products and Biomedical Research, 1(2) (2015)

"Synthesis of Substituted Tetrahydroindoloisoquinoline Derivatives via
Intramolecular Pd-Catalyzed Alkene Carboamination Reactions"

Alicea J and Wolfe PJ

The Journal of Organic Chemistry, 79(9), 4212-4217 (2014)

"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)

Global Trade Item Number

SKU	GTIN
563013-10G	04061832583747