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3355-28-0

3355-28-0 Structure

3355-28-0 Structure
IdentificationMore
[Name]

1-BROMO-2-BUTYNE
[CAS]

3355-28-0
[Synonyms]

1-BROMO-2-BUTYNE
2-BUTYNYL BROMIDE
1-BROMO-2-BUTYNE 98%
[EINECS(EC#)]

608-891-3
[Molecular Formula]

C4H5Br
[MDL Number]

MFCD00190233
[Molecular Weight]

132.99
[MOL File]

3355-28-0.mol
Chemical PropertiesBack Directory
[Appearance]

Clear pale yellow-greenish liquid
[Boiling point ]

40-41 °C/20 mmHg (lit.)
[density ]

1.519 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.508(lit.)
[Fp ]

97 °F
[storage temp. ]

Flammables area
[solubility ]

Miscible with acetonitrile.
[form ]

Liquid
[color ]

Clear pale yellow-greenish
[Specific Gravity]

1.519
[BRN ]

605306
[InChI]

InChI=1S/C4H5Br/c1-2-3-4-5/h4H2,1H3
[InChIKey]

LNNXOEHOXSYWLD-UHFFFAOYSA-N
[SMILES]

C(Br)C#CC
[CAS DataBase Reference]

3355-28-0(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)Exclamation Mark (GHS07)
GHS02,GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335-H226
[Precautionary statements ]

P261-P303+P361+P353-P305+P351+P338-P405-P501a-P210-P233-P240-P241+P242+P243-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P403+P235-P501
[Risk Statements ]

R10:Flammable.
[Safety Statements ]

S16:Keep away from sources of ignition-No smoking .
[RIDADR ]

UN 1993 3/PG 3
[WGK Germany ]

3
[F ]

10-23
[HazardClass ]

3
[PackingGroup ]

III
[HS Code ]

29033990
Hazard InformationBack Directory
[Chemical Properties]

Clear pale yellow-greenish liquid
[Uses]

1-Bromo-2-butyne is used in the preparation of six to eight annulated ring compounds in reaction with indoles and pseudopterane (+/-)-Kallolide B, which is a marine natural product. Further, it acts as a precursor in the preparation of axially chiral teranyl compounds, alkylation of L-tryptophan methyl ester, 4-butynyloxybenzene sulfonyl chloride and mono-propargylated diene derivative. In addition to this, it is also used in the synthesis of isopropylbut-2-ynylamine, allenylcyclobutanol derivatives, allyl-[4-(but-2-ynyloxy)phenyl]sulfane, allenylindium and axially chiral teranyl compounds.
[Preparation]

1-bromo-2-butyne is obtained by reacting 2-butyn-1-ol and organic solvent, pyridine.First react bromoethane with metal magnesium in THF to prepare Grignard reagent, then add paraformaldehyde to Grignard reagent for Grignard reaction, separate and recover after Grignard reaction 2-butyn-1-ol, then mix 2-butyn-1-ol with organic solvent and pyridine, add phosphorus tribromide dropwise for bromination reaction, separate and recover the product after bromination reaction.
[General Description]

1-Bromo-2-butyne is a propargyl bromide derivative. It is one of the constitutional isomer of bromo butyne. Its Br-loss threshold photoionization breakdown diagram has been analyzed to derive dissociative photoionization thresholds to C4H5+ production. It participates in the preparation of linagliptin.
Spectrum DetailBack Directory
[Spectrum Detail]

1-BROMO-2-BUTYNE(3355-28-0)MS
1-BROMO-2-BUTYNE(3355-28-0)1HNMR
1-BROMO-2-BUTYNE(3355-28-0)IR1
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

1-Bromo-2-butyne, 98%(3355-28-0)
[Alfa Aesar]

1-Bromo-2-butyne, 98%(3355-28-0)
[Sigma Aldrich]

3355-28-0(sigmaaldrich)
[TCI AMERICA]

1-Bromo-2-butyne,>96.0%(GC)(3355-28-0)
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