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2-Bromothiophene CAS 1003-09-4

2-Bromothiophene - Names and IdentifiersName2-BromothiopheneSynonymsINDIP-0202-Bromothiophene2-

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2-Bromothiophene - Names and Identifiers

Name2-Bromothiophene
SynonymsINDIP-020
2-Bromothiophene
2-BROMOTHIOPHENE
2-BROMO THIOPHENE
2-Thienyl bromide
2-THIENYL BROMIDE
TIMTEC-BB SBB003931
2 - broMine thiophene
Clopidogrel Impurity 74
CAS1003-09-4
EINECS213-699-4
InChIInChI=1/C4H3BrS/c5-4-2-1-3-6-4/h1-3H
InChIKeyTUCRZHGAIRVWTI-UHFFFAOYSA-N

2-Bromothiophene - Physico-chemical Properties

Molecular FormulaC4H3BrS
Molar Mass163.04
Density1.684 g/mL at 25 °C (lit.)
Melting Point-10 °C
Boling Point149-151 °C (lit.)
Flash Point140°F
Water SolubilityIMMISCIBLE
Vapor Presure4.99mmHg at 25°C
AppearanceLiquid
Specific Gravity1.684
ColorClear colorless to slightly brownish
BRN104663
Storage Condition2-8°C
SensitiveLight Sensitive
Refractive Indexn20/D 1.586(lit.)
Physical and Chemical PropertiesProperty: colorless to light yellow liquid

2-Bromothiophene - Risk and Safety

Risk CodesR10 - Flammable
R25 - Toxic if swallowed
R41 - Risk of serious damage to eyes
R51/53 - Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. 
R36/37/38 - Irritating to eyes, respiratory system and skin.
R23/24 -
R22 - Harmful if swallowed
R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. 
S16 - Keep away from sources of ignition.
S36 - Wear suitable protective clothing.
UN IDsUN 2929 6.1/PG 2
WGK Germany3
FLUKA BRAND F CODES8
TSCAT
HS Code29349990
Hazard NoteIrritant
Hazard Class6.1
Packing GroupII

2-Bromothiophene - Reference Information

NIST chemical information information provided by: webbook.nist.gov (external link)
EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
Use for organic synthesis.
use as an intermediate of the antithrombotic drug clopidogrel
2-thienyl Ester was prepared with CuBr-LiBr and chloroform-treated Grignard reagents.
production method results from bromination of thiophene. Thiophene was dissolved in acetic acid and a solution of bromine in glacial acetic acid was added below 10 °c. Water was then added to the reaction mixture to precipitate an oily liquid. Extract with diethyl ether. The acetic acid was removed by adding potassium carbonate to the extract, dried, distilled off diethyl ether, and then distilled under reduced pressure to obtain 2-46 ° C. (1.73kPa) fractions to obtain 2-bromothiophene in a yield of 55%.

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