5-Bromothiophene-2-carbaldehyde

5-Bromothiophene-2-carbaldehyde Basic information

Product Name:	5-Bromothiophene-2-carbaldehyde
Synonyms:	2-Thiophenecarboxaldehyde, 5-bromo-;LABOTEST-BB LT00112291;5-BROMO-2-THIOPHENECARBALDEHYDE;5-BROMO-2-THIOPHENECARBOXALDEHYDE;5-BROMO-2-FORMYLTHIOPHENE;5-BROMOTHIOPHENE-2-ALDEHYDE;5-BROMO-THIOPHENE-2-CARBALDEHYDE;5-BROMOTHIOPHENE-2-CARBOXALDEHYDE
CAS:	4701-17-1
MF:	C5H3BrOS
MW:	191.05
EINECS:	225-176-8
Product Categories:	Heterocycle-oher series;alkyl bromide;Azoles;blocks;Bromides;Thiophenes & Benzothiophenes;Heterocycles;Aldehydes;Thiophenes & Benzothiophenes;bc0001
Mol File:	4701-17-1.mol

5-Bromothiophene-2-carbaldehyde Chemical Properties

Melting point	55°C
Boiling point	105-107 °C11 mm Hg(lit.)
density	1.607 g/mL at 25 °C(lit.)
refractive index	n20/D 1.637(lit.)
Fp	210 °F
storage temp.	2-8°C
solubility	Soluble in chloroform and methanol.
form	Liquid After Melting
color	Clear yellow to brown
Sensitive	Air Sensitive
BRN	108404
InChIKey	GFBVUFQNHLUCPX-UHFFFAOYSA-N
LogP	2.566 (est)
CAS DataBase Reference	4701-17-1(CAS DataBase Reference)
NIST Chemistry Reference	5-Bromo-2-thiophenecarboxaldehyde(4701-17-1)

Safety Information

MSDS Information

5-Bromothiophene-2-carbaldehyde Usage And Synthesis

Chemical Properties	clear yellow to brown liquid after melting
Uses	5-Bromo-2-thiophenecarboxaldehyde was used to prepare 5-[18F]fluoro-2-2-thiophene carboxaldehyde. Also is used in biological studies as anti-inflammatory and anti-tumor activity of the marine mangrove Rhizophora apiculata.
Synthesis Reference(s)	Journal of the American Chemical Society, 72, p. 1422, 1950 DOI: 10.1021/ja01159a527

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

Raw materials	N,N-Dimethylformamide-->Carbon tetrachloride-->Chlorobenzene-->Phosphorus oxybromide-->Triphosgene-->N-Methylformanilide-->2-Bromothiophene-->Thiophene, 2-bromo-5-(chloromethyl)--->2-Bromo-5-methylthiophene-->5-Bromo-2-thiophenecarboxylic acid-->5-BROMOTHIOPHEN-2-YLMETHYLAMINE-->Ethyl 5-bromothiophene-2-carboxylate
Preparation Products	[2，2’]bithiophenyl-5,5'-dicarbaldehyde-->5-BROMO-2,2'-BITHIOPHENE-5'-CARBOXALDEHYDE-->1-(5-BROMOTHIEN-2-YL)ETHANAMINE-->2-Propenoic acid, 3-(5-broMo-2-thienyl)-

Login