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553352

Sigma-Aldrich

5-Bromo-2,3-dimethoxybenzaldehyde

97%

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About This Item

Linear Formula:
BrC6H2(OCH3)2CHO
CAS Number:
Molecular Weight:
245.07
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

mp

81-84 °C (lit.)

SMILES string

COc1cc(Br)cc(C=O)c1OC

InChI

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

InChI key

RVMWFOFQRYTRHZ-UHFFFAOYSA-N

General description

5-Bromo-2,3-dimethoxybenzaldehyde can be prepared by employing 5-bromo-2-hydroxy-3-methoxybenzaldehyde as a starting reagent.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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 cyclisation of benzylaminonitriles. Part 7. Regiospecific formation of methoxy-substituted isoquinolin-4-ones using methylthio activating groups.
Gavin JP and Waigh RD.
Journal of the Chemical Society. Perkin Transactions 1, 3, 503-508 (1990)
Flavonoids syntheses. V. Synthesis of flavonoids with three hydroxy and four methoxy groups and their spectral properties.
Iinuma M, et al.
Chemical & Pharmaceutical Bulletin, 35(2), 660-667 (1987)

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