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1-Phenyl-1H-benzotriazole

Product Name
1-Phenyl-1H-benzotriazole
CAS No.
883-39-6
Chemical Name
1-Phenyl-1H-benzotriazole
Synonyms
1-phenylbenzotriazole;1-Phenyl-1H-benzotriazole;1H-Benzotriazole, 1-phenyl-;1-Phenyl-1H-benzo[d][1,2,3]triazole
CBNumber
CB12304572
Molecular Formula
C12H9N3
Formula Weight
195.22
MOL File
883-39-6.mol
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1-Phenyl-1H-benzotriazole Property

Melting point:
108-109 °C
Boiling point:
359.3±25.0 °C(Predicted)
Density 
1.21±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
0.82±0.30(Predicted)
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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
P319963
Product name
1-Phenyl-1H-benzo[d][1,2,3]triazole
Packaging
100mg
Price
$60
Updated
2021/12/16
Oakwood
Product number
382479
Product name
1-Phenyl-1H-benzo[d][1,2,3]triazole
Purity
97%
Packaging
10mg
Price
$125
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0983064
Product name
1-PHENYL-1H-BENZOTRIAZOLE
Purity
95.00%
Packaging
5MG
Price
$504.76
Updated
2021/12/16
Crysdot
Product number
CD11034770
Product name
1-Phenyl-1H-benzo[d][1,2,3]triazole
Purity
95+%
Packaging
1g
Price
$218
Updated
2021/12/16
Alichem
Product number
883396
Product name
1-Phenyl-1H-benzo[d][1,2,3]triazole
Packaging
1g
Price
$224.4
Updated
2021/12/16
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1-Phenyl-1H-benzotriazole Chemical Properties,Usage,Production

Uses

1-Phenyl-1H-benzo[d][1,2,3]triazole is a reagent used in the prepartion of possible surrogates for kobayashi’s aryne precursors.

Synthesis

95-14-7

591-50-4

883-39-6

GENERAL METHODS: Cu(OAc)2-H2O (0.01 mmol) was dissolved in DMF (2 mL) under nitrogen protection, and iodobenzene (1.2 mmol), benzotriazole (1.0 mmol), and Cs2CO3 (2 mmol) were added sequentially. The reaction system was stirred at 110 °C for 24 hours. After completion of the reaction, it was cooled to room temperature and the reaction mixture was partitioned between water and ethyl acetate. The organic phase was separated and the aqueous phase was extracted with ethyl acetate. The organic phases were combined, washed with saturated brine, dried over anhydrous Na2SO4 and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to afford the target product 1-phenyl-1H-benzo[d][1,2,3]triazole.

References

[1] Tetrahedron Letters, 1998, vol. 39, # 31, p. 5617 - 5620
[2] RSC Advances, 2015, vol. 5, # 51, p. 40628 - 40635
[3] Synthetic Communications, 2012, vol. 42, # 15, p. 2217 - 2228
[4] Journal of Organic Chemistry, 2004, vol. 69, # 17, p. 5578 - 5587
[5] Synthesis, 2012, vol. 44, # 7, p. 1063 - 1068

1-Phenyl-1H-benzotriazole Preparation Products And Raw materials

Raw materials

Preparation Products

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883-39-6, 1-Phenyl-1H-benzotriazoleRelated Search:


  • 1-Phenyl-1H-benzotriazole
  • 1-phenylbenzotriazole
  • 1-Phenyl-1H-benzo[d][1,2,3]triazole
  • 1H-Benzotriazole, 1-phenyl-
  • 883-39-6