|  | |  |  | 1-BROMO-2-BUTYNE Basic information | 
|  |  | 1-BROMO-2-BUTYNE Chemical Properties | 
 | 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. | Inert atmosphere,Room Temperature |  | solubility | Miscible with acetonitrile. |  | form | Liquid |  | Specific Gravity | 1.519 |  | color | Clear pale yellow-greenish |  | BRN | 605306 |  | InChIKey | LNNXOEHOXSYWLD-UHFFFAOYSA-N |  | CAS DataBase Reference | 3355-28-0(CAS DataBase Reference) | 
| Risk Statements | 10 |  | Safety Statements | 16-24/25 |  | RIDADR | UN 1993 3/PG 3 |  | WGK Germany | 3 |  | F | 10-23 |  | HazardClass | 3 |  | PackingGroup | III |  | HS Code | 29033990 | 
|  |  | 1-BROMO-2-BUTYNE Usage And Synthesis | 
 | 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. | 
|  |  | 1-BROMO-2-BUTYNE Preparation Products And Raw materials | 
 |