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ChemicalBook--->CAS DataBase List--->1214264-88-6

1214264-88-6

1214264-88-6 Structure

1214264-88-6 Structure
IdentificationBack Directory
[Name]

1-pinacolato-2-(1,8)diamo-naphthalenylborane
[CAS]

1214264-88-6
[Synonyms]

(Pin)B-B(Dan)
2-(4,4,5,5-Tetra
1-pinacolato-2-(1,8)diamo-naphthalenylborane
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-...
1H-Naphtho[1,8-de][1,3,2]diazaborinine-2(3H)-boronic Acid Pinacol Ester
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-naphtho[1,8-de][1,3,2]diazaborinane
3-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,4-diaza-3-boratricyclo-[7.3.1.0^{5,13}]trideca-1(13)
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine
1H-Naphtho[1,8-de]-1,3,2-diazaborine, 2,3-dihydro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
3-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,4-diaza-3-boratricyclo-[7.3.1.0 {5,13}]trideca-1(13),5,7,9,11- pentaene
3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,4-diaza-3-boratricyclo[7.3.1.0?13]trideca-1(13),5,7,9,11-pentaene
[Molecular Formula]

C16H20B2N2O2
[MDL Number]

MFCD27980593
[MOL File]

1214264-88-6.mol
[Molecular Weight]

293.96
Chemical PropertiesBack Directory
[Melting point ]

186.7-187.4 °C
[Boiling point ]

384.1±25.0 °C(Predicted)
[density ]

1.14±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

solid
[pka]

-0.85±0.20(Predicted)
[color ]

Off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

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

P260-P280-P301+P310-P302+P350-P302+P352-P304+P340
[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

1-pinacolato-2-(1,8)diamo-naphthalenylborane(1214264-88-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

1,8-Diaminonaphthalene

479-27-6

Bis(pinacolato)diboron

73183-34-3

1-pinacolato-2-(1,8)diamo-naphthalenylborane

1214264-88-6

General Steps: EXAMPLE: A 50 mL reaction flask was placed on a magnetic stirrer and pinacol ester of bisboronic acid (1.0 mmol, 1.0 eq.), 1,8-diaminonaphthalene (1.0 mmol, 1.0 eq.), and sodium methanol (1.0 mmol, 1.0 eq.) were added sequentially. After purging the reaction system with nitrogen three times under nitrogen protection, 10 mL of methanol was added as solvent. The reaction mixture was heated to 70 °C and stirred continuously for 4 hours. After completion of the reaction, the solvent methanol was removed by rotary evaporator. The crude product was purified by column chromatography to afford the target product 1-pinacol-2-(1,8)naphthalenediamine biboronate in 90% yield.

[References]

[1] Patent: CN106946916, 2017, A. Location in patent: Paragraph 0012
[2] Chemical Communications, 2014, vol. 50, # 61, p. 8299 - 8302
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