ChemicalBook > CAS DataBase List > 6-BROMOTETRAZOLO[1,5-A]PYRIDINE

6-BROMOTETRAZOLO[1,5-A]PYRIDINE

Product Name
6-BROMOTETRAZOLO[1,5-A]PYRIDINE
CAS No.
5799-75-7
Chemical Name
6-BROMOTETRAZOLO[1,5-A]PYRIDINE
Synonyms
1-(Prop-2-yn-1-yl)piperidine;1-(prop-2-ynyl)piperidine;1-(2-Propyn-1-yl)piperidine;Piperidine, 1-(2-propyn-1-yl)-
CBNumber
CB42457639
Molecular Formula
C8H13N
Formula Weight
123.2
MOL File
5799-75-7.mol
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6-BROMOTETRAZOLO[1,5-A]PYRIDINE Property

Boiling point:
55-57 °C(Press: 12 Torr)
Density 
0.8944 g/cm3
pka
7.78±0.10(Predicted)
InChI
InChI=1S/C8H13N/c1-2-6-9-7-4-3-5-8-9/h1H,3-8H2
InChIKey
LQSQLFOKTMSBEC-UHFFFAOYSA-N
SMILES
N1(CC#C)CCCCC1
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
B524378
Product name
1-(prop-2-yn-1-yl)piperidine
Packaging
50mg
Price
$60
Updated
2021/12/16
TRC
Product number
B524378
Product name
1-(prop-2-yn-1-yl)piperidine
Packaging
250mg
Price
$200
Updated
2021/12/16
AK Scientific
Product number
8568AB
Product name
1-(Prop-2-yn-1-yl)piperidine
Packaging
250mg
Price
$253
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0311382
Product name
1-(PROP-2-YN-1-YL)PIPERIDINE
Purity
95.00%
Packaging
5MG
Price
$505.02
Updated
2021/12/16
AK Scientific
Product number
8568AB
Product name
1-(Prop-2-yn-1-yl)piperidine
Packaging
10g
Price
$1593
Updated
2021/12/16
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6-BROMOTETRAZOLO[1,5-A]PYRIDINE Chemical Properties,Usage,Production

Synthesis

110-89-4

106-96-7

5799-75-7

General method: Potassium carbonate (25.41 mmol) was added to an N,N-dimethylformamide (DMF) mixture of 3-bromopropargyl (8.47 mmol) and hexahydropyridine (16.94 mmol), and the reaction mixture was stirred at room temperature for 10-12 hours. After completion of the reaction, the reaction mixture was quenched with ice water and extracted with ethyl acetate. The organic layers were combined and dried over anhydrous sodium sulfate, followed by evaporation of the solvent under reduced pressure to give 1-alkynylpiperidine.

References

[1] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 7, p. 1795 - 1801
[2] Organometallics, 2011, vol. 30, # 20, p. 5471 - 5479
[3] European Journal of Medicinal Chemistry, 2015, vol. 99, p. 36 - 50
[4] Journal of the American Chemical Society, 2013, vol. 135, # 34, p. 12627 - 12633
[5] Journal of Medicinal Chemistry, 2001, vol. 44, # 17, p. 2719 - 2734

6-BROMOTETRAZOLO[1,5-A]PYRIDINE Preparation Products And Raw materials

Raw materials

Preparation Products

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6-BROMOTETRAZOLO[1,5-A]PYRIDINE Suppliers

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5799-75-7, 6-BROMOTETRAZOLO[1,5-A]PYRIDINERelated Search:


  • 1-(prop-2-ynyl)piperidine
  • 1-(Prop-2-yn-1-yl)piperidine
  • Piperidine, 1-(2-propyn-1-yl)-
  • 1-(2-Propyn-1-yl)piperidine
  • 5799-75-7