3-Bromothiophene-2-carbaldehyde

3-Bromothiophene-2-carbaldehyde Basic information

Product Name:	3-Bromothiophene-2-carbaldehyde
Synonyms:	BUTTPARK 43\57-52;3-BROMOTHIOPHENE-2-CARBOXALDEHYDE;3-BROMOTHIOPHENE-2-CARBALDEHYDE;3-BROMO-2-FORMYLTHIOPHENE;3-BROMO-2-THIOPHENECARBALDEHYDE;3-Bromothiophene-2-carboxaldehyde, 95%+;3-Bromo-2-Formylthophene;3-Bromothiophene-2-carboxaldehyde, GC 97%
CAS:	930-96-1
MF:	C5H3BrOS
MW:	191.05
EINECS:	672-838-0
Product Categories:	Aldehydes;Building Blocks;C1 to C6;C4 to C6;Carbonyl Compounds;Chemical Synthesis;Azoles;blocks;Bromides;Thiophene&Benzothiophene;Functional Materials;Heterocyclic Building Blocks;Organic Building Blocks;Thiophenes;Reagents for Conducting Polymer Research;Thiophene Derivatives (for Conduting Polymer Research);Thiophen
Mol File:	930-96-1.mol

3-Bromothiophene-2-carbaldehyde Chemical Properties

Melting point	25 °C
Boiling point	77-79°C 0,2mm
density	1.755 g/mL at 25 °C
refractive index	1.6377
Fp	110-113°C/10mm
storage temp.	Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
form	clear liquid
color	Light yellow to Amber to Dark green
Water Solubility	Not miscible in water.
Sensitive	Air Sensitive
BRN	109757
InChIKey	BCZHCWCOQDRYGS-UHFFFAOYSA-N
CAS DataBase Reference	930-96-1(CAS DataBase Reference)

Safety Information

MSDS Information

Provider	Language
ALFA	English

3-Bromothiophene-2-carbaldehyde Usage And Synthesis

Chemical Properties	Colorless to yellow liquid
Uses	3-Bromothiophene-2-carboxaldehyde is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.
Synthesis Reference(s)	Journal of Medicinal Chemistry, 34, p. 1805, 1991 DOI: 10.1021/jm00110a008

3-Bromothiophene-2-carbaldehyde Preparation Products And Raw materials

Raw materials	Diethyl ether-->Tetrahydrofuran-->N,N-Dimethylformamide-->n-Butyllithium-->Nitrogen-->Lithium diisopropylamide-->3-Bromothiophene-->2,3-Dibromothiophene
Preparation Products	TETRABROMO-THIENO[3,2-B]THIOPHENE-->3-BROMOTHIOPHENE-2-CARBONITRILE-->Thieno[3,2-b]thiophene-2-carbonitrile-->2-BROMOTHIOPHENE-3-CARBALDEHYDE-->4-Bromothiophene-2-carboxaldehyde-->2-ACETYL-3-BROMOTHIOPHENE-->3-BROMOTHIOPHENE-2-CARBOXALDEHYDE DIETHYL ACETAL-->3-azidothiophene-2-carbaldehyde-->2-Thiophenecarboxaldehyde, 3-ethynyl- (9CI)-->3-bromo-2-(chloromethyl)thiophene

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