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4，5-Dibromothiophene-2-carboxaldehyde - 98%, high purity , CAS No.38071-22-6

COA

Grade & Purity:

≥98%

Cas Number: 38071-22-6
Molecular Weight: 269.94
MDL number: MFCD00225242
PubChem CID: 813164

In stock

Item Number

D133408

Grouped product items
SKU	Size	Availability	Price	Qty
D133408-5g	5g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$103.90
D133408-25g	25g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$400.90

Basic Description

Synonyms	4,5-dibromothiophene-2-carbaldehyde \| 38071-22-6 \| 4,5-DIBROMOTHIOPHENE-2-CARBOXALDEHYDE \| 4,5-Dibromo-thiophene-2-carbaldehyde \| CHEMBL596225 \| SCHEMBL947395 \| 4,5-dibromo-2-formylthiophene \| DTXSID80355661 \| CHRAVDVWAPGZOY-UHFFFAOYSA-N \| 4,5-dibromo-2-thiophenecarbaldehy
Specifications & Purity	≥98%
Shipped In	Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Thiophenes
    - Subclass 2,3,5-trisubstituted thiophenes

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Thiophenes
Subclass	2,3,5-trisubstituted thiophenes
Intermediate Tree Nodes	Not available
Direct Parent	2,3,5-trisubstituted thiophenes
Alternative Parents	Aryl-aldehydes Aryl bromides Heteroaromatic compounds Organobromides Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	2,3,5-trisubstituted thiophene - Aryl-aldehyde - Aryl halide - Aryl bromide - Heteroaromatic compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organobromide - Organohalogen compound - Aldehyde - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as 2,3,5-trisubstituted thiophenes. These are organic compounds containing a thiophene that is trisubstituted at the C-2, C3- and C5-positions.
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	4,5-dibromothiophene-2-carbaldehyde
INCHI	InChI=1S/C5H2Br2OS/c6-4-1-3(2-8)9-5(4)7/h1-2H
InChIKey	CHRAVDVWAPGZOY-UHFFFAOYSA-N
Smiles	C1=C(SC(=C1Br)Br)C=O
Isomeric SMILES	C1=C(SC(=C1Br)Br)C=O
Molecular Weight	269.94
Reaxy-Rn	2585
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2585&ln=

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

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

Analytical Chart:

Chemical and Physical Properties

Molecular Weight	269.940 g/mol
XLogP3	3.100
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	1
Exact Mass	269.817 Da
Monoisotopic Mass	267.819 Da
Topological Polar Surface Area	45.300 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	120.000
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

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