ChemicalBook--->CAS DataBase List--->55981-29-8

55981-29-8

55981-29-8 Structure

55981-29-8 Structure
IdentificationBack Directory
[Name]

1,3,4-Thiadiazole, 2,5-dibroMo-
[CAS]

55981-29-8
[Synonyms]

2,5-DibroMothiadiazole
2,5-DibroMo-1,3,4-thiadiazole
1,3,4-Thiadiazole, 2,5-dibroMo-
[EINECS(EC#)]

692-177-1
[Molecular Formula]

C2Br2N2S
[MDL Number]

MFCD00466397
[MOL File]

55981-29-8.mol
[Molecular Weight]

243.91
Chemical PropertiesBack Directory
[Melting point ]

112-113°
[Boiling point ]

289.4±23.0 °C(Predicted)
[density ]

2.495±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

-2.77±0.10(Predicted)
[Appearance]

White to yellow Solid
[InChI]

InChI=1S/C2Br2N2S/c3-1-5-6-2(4)7-1
[InChIKey]

MNHUBBRVPVSVCM-UHFFFAOYSA-N
[SMILES]

S1C(Br)=NN=C1Br
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P260-P280-P312
[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

1,3,4-Thiadiazole, 2,5-dibroMo-(55981-29-8)13CNMR
Hazard InformationBack Directory
[Synthesis]

2-AMINO-5-BROMO-[1,3,4]THIADIAZOLE

37566-39-5

1,3,4-Thiadiazole, 2,5-dibroMo-

55981-29-8

General procedure for the synthesis of 2,5-dibromo-1,3,4-thiadiazole from 2-amino-5-bromo-1,3,4-thiadiazole: 2-amino-5-bromo-1,3,4-thiadiazole (20 g, 0.111 mol) was slowly added under nitrogen protection to a non-homogeneous mixture containing CuBr2 (29.8 g, 1.2 eq.) and t-BuNO2 (19.8 mL, density = 0.867 g/mL) in a non-homogeneous mixture of MeCN (600 mL, 0.2 M solution), taking care to control the rate of addition to avoid intense exotherm. The reaction mixture was stirred overnight at room temperature. Upon completion of the reaction, the reaction was quenched with 600 mL of saturated aqueous NH4Cl solution and then extracted with ether. The organic layer was dried with MgSO4, filtered and concentrated in vacuum to give the crude product. The crude product was ground in 200 mL MeOH and the solid was collected by filtration to afford the target compound 2,5-dibromo-1,3,4-thiadiazole (18.7 g, 70% yield).

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 2, p. 861 - 864
[2] Macromolecules, 2005, vol. 38, # 4, p. 1500 - 1503
[3] Patent: WO2010/45303, 2010, A2. Location in patent: Page/Page column 97
[4] ACS Medicinal Chemistry Letters, 2012, vol. 3, # 3, p. 198 - 202
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