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459-64-3

459-64-3 Structure

459-64-3 Structure
IdentificationBack Directory
[Name]

4-METHOXYBENZENEDIAZONIUM TETRAFLUOROBORATE
[CAS]

459-64-3
[Synonyms]

4-Mebenzenediazonium tetrafluoroborate
MethoxybenzenediazoniuM tetrafluoroborate
4-METHOXYBENZENEDIAZONIUM TETRAFLUOROBORATE
4-MethoxybenzenediazoniumTetrafluoroborate98%
[EINECS(EC#)]

207-296-2
[Molecular Formula]

C7H7BF4N2O
[MDL Number]

MFCD00011897
[MOL File]

459-64-3.mol
[Molecular Weight]

221.95
Chemical PropertiesBack Directory
[Appearance]

grey-brown powder
[Melting point ]

142-144 °C(lit.)
[storage temp. ]

Refrigerator (+4°C)
[form ]

powder to crystal
[color ]

White to Orange to Green
[Water Solubility ]

Decompose in water
[λmax]

315nm(CHCl3)(lit.)
[BRN ]

3579591
[InChI]

InChI=1S/C7H7N2O.BF4/c1-10-7-4-2-6(9-8)3-5-7;2-1(3,4)5/h2-5H,1H3;/q+1;-1
[InChIKey]

CNKRQRKNUIYISU-UHFFFAOYSA-M
[SMILES]

[B-](F)(F)(F)F.C1(OC)=CC=C([N+]#N)C=C1
Hazard InformationBack Directory
[Chemical Properties]

grey-brown powder
[Uses]

4-Methoxybenzenediazonium tetrafluoroborate has been used in the preparation of azo coupled cyclic β-enaminones.
[General Description]

Interaction of 4-methoxybenzenediazonium tetrafluoroborate with synthetic DOPA-melanin and its precursors has been studied using EPR spectroscopy and spin-trapping technique.
[Synthesis]

Hydrogen fluoride

7664-39-3

Boric acid

11113-50-1

p-Anisidine

104-94-9

4-METHOXYBENZENEDIAZONIUM TETRAFLUOROBORATE

459-64-3

The general procedure for the synthesis of tetrafluoroborate-4-methoxybenzenediazonium ortho ester from hydrofluoric acid, boric acid and p-aminoanisole was as follows: first, a mixture of aqueous hydrofluoric acid (2.08 g, 104 mmol, 17.2 eq.), boric acid (2.29 g, 26.0 mmol, 4.3 eq.), and water (5 mL) was added to p-aminomethyl ether (6.0 mmol). After stirring for 5 minutes, sodium nitrite (765 mg, 11.1 mmol, 1.9 eq.) was added in portions over 3 minutes at room temperature. After 15 minutes of reaction, the precipitate formed was filtered, washed with ether (5 mL) and subsequently suspended in acetonitrile (10 mL), filtered again and dissolved in acetonitrile (4 mL). Finally, after the addition of ether, the precipitate formed was filtered and dried under reduced pressure to give pure n-phenyl tetrafluoroborate-4-methoxy diazepine.

[References]

[1] Beilstein Journal of Organic Chemistry, 2015, vol. 11, p. 1494 - 1502
Safety DataBack Directory
[Hazard Codes ]

C
[Risk Statements ]

34
[Safety Statements ]

26-36/37/39-45
[RIDADR ]

UN 3261 8/PG 2
[WGK Germany ]

3
[F ]

10-21
[HazardClass ]

8
[PackingGroup ]

III
[HS Code ]

29270000
[Storage Class]

8A - Combustible corrosive hazardous materials
[Hazard Classifications]

Eye Dam. 1
Skin Corr. 1B
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Diethyl ether-->Sodium nitrite-->Acetone-->Fluoroboric acid-->p-Anisidine-->Sulfamic acid-->Hydrogen fluoride-->Boric acid
[Preparation Products]

4,4'-Dimethoxybiphenyl-->trans-O-Methyl-p-coumaric acid-->ETHYL 4-FORMYL-1-(4-METHOXYPHENYL)-1H-PYRAZOLE-3-CARBOXYLATE-->2-(4-Methoxybenzenesulfonyl)acetonitrile
Spectrum DetailBack Directory
[Spectrum Detail]

4-METHOXYBENZENEDIAZONIUM TETRAFLUOROBORATE(459-64-3)1HNMR
4-METHOXYBENZENEDIAZONIUM TETRAFLUOROBORATE(459-64-3)Raman
4-METHOXYBENZENEDIAZONIUM TETRAFLUOROBORATE(459-64-3)FT-IR
4-METHOXYBENZENEDIAZONIUM TETRAFLUOROBORATE(459-64-3)IR
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