Chemical Name | Boron trifluoride acetic acid |
MDL Number | MFCD00036359 |
CAS Number | 373-61-5 |
PubChem Substance ID | 11116786 |
EC Number | 206-768-5 |
Beilstein Registry Number | 3686517 |
Synonym |
ACETIC ACID-BORON TRIFLUORIDE COMPLEX
Aceticacidborontrifluoride(2:1)
BORON TRIFLUORIDE DIACETIC ACID COMPLEX
BORON TRIFLUORIDE-ACETIC ACID
Borate(1-), bis(acetato-.kappa.O)difluoro-, hydrogen fluoride (1:2:1), (T-4)-
Borate(1-),bis(acetato-O)difluoro-,dihydrogenfluoride,(T-4)-
Boron trifluoride acetic acid complex
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Chemical Name Translation | 三氟化硼-乙酸 |
InChIKey | OVYKFNOIPQYMRU-UHFFFAOYSA-K |
LabNetwork Molecule ID | LN00223529 |
InChI | InChI=1S/2C2H4O2.BF3/c2*1-2(3)4;2-1(3)4/h2*1H3,(H,3,4); |
Canonical SMILES | O=C(OB(F)(F)OC(C)=O)C.[F-].[H+] |
GHS Symbol
WGK Germany | 3 |
Hazard statements | |
- H314 Causes severe skin burns and eye damage 导致严重的皮肤灼伤和眼睛损伤
- H302 Harmful if swallowed 吞食有害
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Personal Protective Equipment |
Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter |
Precautionary statements | |
- P310 Immediately call a POISON CENTER or doctor/physician. 立即呼救解毒中心或医生/医师。
- P280 Wear protective gloves/protective clothing/eye protection/face protection. 戴防护手套/防护服/眼睛的保护物/面部保护物。
- P305+P351+P338
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Signal word |
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Packing Group | II |
UN Number |
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Risk Statements | |
- R22 Harmful if swallowed 吞咽有害
- R34 Causes burns 会导致灼伤
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Safety Statements | |
- S25 Avoid contact with eyes 避免眼睛接触;
- 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;
- 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);
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Storage condition |
Moisture Sensitive
N/A
N/A℃
No Data Available
避免潮湿。 |
Hazard Codes |
C |
{ALD} Beilstein: 2,IV,95
{ALF} Mild acid catalyst which has found use as a desilylating agent: Allylsilanes undergo desilylation, via ß-stabilized carbocations, to give alkenes with allylic rearrangement: Tetrahedron Lett., 446 (1979); J. Chem. Soc., Perkin 1, 3267 (1992). -Silyl tertiary alcohols undergo a pinacol-like rearrangement to give alkenes: Tetrahedron Lett., 22, 2321 (1981). Has been used in the protodesilylation of the phenyl group as part of the conversion of the dimethylphenylsilyl group into a hydroxyl group with retention of configuration: J. Chem. Soc., Perkin 1, 317 (1995). For reaction scheme, see Chlorodimethyl­phenyl­silane, A15638.