Chemical Name |
Nitrosoniumtetrafluoroborate |
Synonym |
四氟硼酸亚硝 tetrafluoro-borate(1-nitrosyl Nitrosonium fluoroborate Nitrosoniumtetrafluoroborate98% nitrosium tetrafluoroborate NITROSYL TETRAFLUOROBORATE Nitrosonium tetrafluoroborate, min. 97% Nitrosoniumtetrafluoroborate,min.97% NITROSONIUM (NITROSYL) TETRAFLUOROBORATE NITROSONIUM TETRAFLUOROBORATE Nitrosonium tetrafluoroborate 98% |
MDL Number |
MFCD00011433 |
PubChem Substance ID |
24850360 |
EC Number |
238-679-2 |
CAS Number |
14635-75-7 |
Merck Number |
14,6649 |
Beilstein Registry Number |
2384789 |
Chemical Name Translation |
亚硝鎓四氟硼酸盐 |
GHS Symbol
WGK Germany |
3 |
Precautionary statements |
|
|
Signal word |
|
Hazard statements |
|
-
H314
Causes severe skin burns and eye damage 导致严重的皮肤灼伤和眼睛损伤
|
Personal Protective Equipment |
Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges |
Safety Statements |
|
-
S45
In case of accident or if you feel unwell seek medical advice immediately (show the label where possible) 发生事故时或感觉不适时,立即求医(可能时出示标签);
-
S26
In case of contact with eyes, rinse immediately with plenty of water and seek medical advice 眼睛接触后,立即用大量水冲洗并征求医生意见;
-
S36/37/39
Wear suitable protective clothing, gloves and eye/face protection 穿戴适当的防护服、手套和眼睛/面保护;
-
S7/8
Keep container tightly closed and dry 保存在严格密闭容器中,保持干燥;
|
Packing Group |
II |
UN Number |
UN3260 |
Risk Statements |
|
|
Storage condition |
Moisture Sensitive 2-8°C |
Hazard Codes |
C |
Hazard Class |
6.1 |
{ALF} With excess reagent, oxidation of the isoxazoline to the isoxazole occurs.
{ALF} Undergoes an interesting insertion reaction with diarylcyclopropanes: Chem. Lett., 233 (1988):
{ALF}
{ALF} Crystalline nitrosating agent: Secondary amines to nitrosamines: Chem. Ber., 89, 2374 (1956); deamination of primary amides: J. Org. Chem., 30, 2386 (1965); conversion of arylhydrazines to azides: Tetrahedron Lett., 28, 5091 (1987). In organic solvents, converts arylamines directly to diazonium tetrafluoroborates which undergo the Balz-Schiemann reaction (see Tetrafluoroboric acid, L14037) in situ to give high yields of aryl fluorides: Chem. Ber., 88, 1939 (1955); EP 430,434 (1991). Methyl or methoxy substituted aromatics in acetonitrile give the nitrosoaromatics in good yield: J. Org. Chem., 59, 5573 (1994).
{ALF} Convenient catalyst for iodination of aromatics by iodide ion with air as oxidant: J. Org. Chem., 53, 3548 (1988), or for addition of iodine (or iodine + nucleophile) to alkenes: Acta Chem. Scand. B, 43, 902 (1989).