JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.

This is a demo store. No orders will be fulfilled.

Account

Settings

Language

྾

Home
Chemistry & Biochemicals
Building Blocks
Organic Building Blocks
6-Bromo-2-pyridinecarboxaldehyde - 97%, high purity , CAS No.34160-40-2

Skip to the end of the images gallery

Skip to the beginning of the images gallery

6-Bromo-2-pyridinecarboxaldehyde - 97%, high purity , CAS No.34160-40-2

1 Citations

COA

Grade & Purity:

≥97%

Cas Number: 34160-40-2
Molecular Weight: 186.01
MDL number: MFCD02683546
PubChem CID: 2757009

In stock

Item Number

B115762

Grouped product items
SKU	Size	Availability	Price
B115762-1g	1g	3	$16.90
B115762-5g	5g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$25.90
B115762-10g	10g	2	$50.90
B115762-25g	25g	1	$125.90
B115762-100g	100g	1	$500.90

View related series

Bromopyridines (172) Halogenated heterocyclic block (1171)

Basic Description

Synonyms	2-Pyridinecarboxaldehyde, 6-bromo- \| 6-bromo-2-pyridine carbaldehyde \| 2-formyl-6-bromopyridine \| 6-Bromopicoline aldehyde \| BCP14423 \| MFCD02683546 \| QWFHFNGMCPMOCD-UHFFFAOYSA-N \| B3716 \| 6-Bromo-2-pyridinecarboxaldehyde \| 6-bromo-2-pyridine-carboxaldehy
Specifications & Purity	≥97%
Storage Temp	Store at 2-8°C,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	6-Bromo-2-pyridinecarboxaldehyde is a pyridine derivative. It participates in the synthesis of meso-substituted trans-A2B2-porphyrin 6-Bromo-2-pyridinecarboxaldehyde may be used in the synthesis of: · 6-([2,2’-bi(1,3-dithiolylidene)]-4-yl)picolinaldehyde · tris(2-pyridylmethyl)amine (Tpy) derivative having Tpy core bearing a 3-formyl-phenyl substituent on one of the three arms · syn- and anti- forms of 4-(6-bromopyridin-2-yl)-3-methyl-3-phenyloxetan-2-one · 6-(2,4,6-triisopropylphenyl)-2-pyridinecarboxaldehyde Substrate used in a study of a rhodium-catalyzed, reductive aldol coupling with divinyl ketones leading to syn ?-hydroxyenones. Useful building block for Tris[(pyridyl)methyl]amine ligands

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Pyridines and derivatives
    - Subclass Pyridine carboxaldehydes

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Pyridines and derivatives
Subclass	Pyridine carboxaldehydes
Intermediate Tree Nodes	Not available
Direct Parent	Pyridine carboxaldehydes
Alternative Parents	Aryl-aldehydes 2-halopyridines Aryl bromides Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organobromides Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	2-pyridine carboxaldehyde - 2-halopyridine - Aryl-aldehyde - Aryl bromide - Aryl halide - Heteroaromatic compound - Azacycle - Aldehyde - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as pyridine carboxaldehydes. These are aromatic compounds containing a pyridine ring which bears a carboxaldehyde group.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	6-bromopyridine-2-carbaldehyde
INCHI	InChI=1S/C6H4BrNO/c7-6-3-1-2-5(4-9)8-6/h1-4H
InChIKey	QWFHFNGMCPMOCD-UHFFFAOYSA-N
Smiles	C1=CC(=NC(=C1)Br)C=O
Isomeric SMILES	C1=CC(=NC(=C1)Br)C=O
WGK Germany	3
Molecular Weight	186.01
Reaxy-Rn	1524300
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1524300&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

11 results found

Lot Number	Certificate Type	Date	Item
F2524297	Certificate of Analysis	Jul 04, 2025	B115762
G2416455	Certificate of Analysis	Apr 03, 2024	B115762
J2330162	Certificate of Analysis	Oct 08, 2023	B115762
J2330164	Certificate of Analysis	Sep 28, 2023	B115762
J2330210	Certificate of Analysis	Sep 28, 2023	B115762
J2330163	Certificate of Analysis	Sep 28, 2023	B115762
F2101081	Certificate of Analysis	Mar 10, 2023	B115762
F2101082	Certificate of Analysis	Mar 09, 2023	B115762
F2101080	Certificate of Analysis	Mar 09, 2023	B115762
D1728008	Certificate of Analysis	Oct 17, 2022	B115762
K2005159	Certificate of Analysis	Aug 15, 2022	B115762

Show more⌵

Chemical and Physical Properties

Solubility	Soluble in dichloromethane, ether, ethyl acetate and methanol. Insoluble in water.
Sensitivity	Air sensitive;Heat sensitive
Melt Point(°C)	81-85°C
Molecular Weight	186.010 g/mol
XLogP3	1.700
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	1
Exact Mass	184.948 Da
Monoisotopic Mass	184.948 Da
Topological Polar Surface Area	30.000 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	107.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Alternative Products

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Na Zhang, Yuying Li, Liduo Chen, Cuiqin Li, Guoliang Mao, Jun Wang. (2021) Synthesis, characterization, and ethylene oligomerization with star iminopyridine nickel(II) complexes. JOURNAL OF COORDINATION CHEMISTRY,

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration

Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.