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594261

Sigma-Aldrich

5-Bromoisoquinoline

98%

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About This Item

Empirical Formula (Hill Notation):
C9H6BrN
CAS Number:
34784-04-8
Molecular Weight:
208.05
MDL number:
MFCD01646405
UNSPSC Code:
12352100
PubChem Substance ID:
24881493
NACRES:
NA.22

Assay

98%

mp

83-87 °C (lit.)

SMILES string

Brc1cccc2cnccc12

InChI

1S/C9H6BrN/c10-9-3-1-2-7-6-11-5-4-8(7)9/h1-6H

InChI key

CYJZJGYYTFQQBY-UHFFFAOYSA-N

Application

Starting material employed in palladium-catalyzed aminomethylation and amination reactions.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

594261-1G:
594261-VAR:
594261-BULK:
594261-5G:

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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3-Bromoquinoline 98%

Sigma-Aldrich

124133

3-Bromoquinoline

Gary A Molander et al.
Organic letters, 9(8), 1597-1600 (2007-03-21)
[reaction: see text] The Suzuki-Miyaura cross-coupling reaction of N,N-dialkylaminomethyltrifluoroborates with aryl halides allows the construction of an aminomethyl aryl linkage through a disconnection based on dissonant reactivity patterns. A variety of these aminomethyltrifluoroborate substrates were prepared in good to excellent
Qilong Shen et al.
Journal of the American Chemical Society, 128(31), 10028-10029 (2006-08-03)
A mild, palladium-catalyzed coupling of aryl halides with ammonia or lithium amide to form primary arylamines as the major product is described. These reactions occurred with excellent selectivity for formation of the primary arylamine over formation of the diarylamine (9.5:1

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