Chemical Name | Trifluoromethanesulfonic Anhydride |
CAS Number | 358-23-6 |
Synonym |
TRIFLUOROMETHANESULFONIC ACID ANHYDRIDE
Trifluoromethylsulfonic acid anhydride
Trifluoromethanesulphonicanhydride99%
trifluormethanesulfonic anhydride
TRIFLUOROMETHANESULFONYL ANHYDRIDE
三氟甲烷磺酸酐
三氟甲磺酸酐 溶液
Tirflic anhydride
TRIFLUOROMETHANESULFONIC ANHYDRIDE SET W ITH 10 X 1 ML
Perfluoromethanesulfonic anhydride solution 三氟甲烷磺酸酐 溶液
Trifluoromethanesulfonic acid anhydride
TRIFLIC ANHYDRIDE
三氟甲磺酸酐,三氟甲基磺酸酐
TriFluoroMethaneSulfonic Anhydride(TFMSAA)
Trifluoromethanesulfonic anhydride
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Trifluoromethanesulfonicanhydride,98%
Trifluorme
TRIFLUOROMETHANESULFONIC ANHYDRIDE, 99+%
Trifluoromethanesufonic anhydride
{uni_ |
MDL Number | MFCD00000408 |
EC Number | 206-616-8 |
Beilstein Registry Number | 1813600 |
PubChem Substance ID | 67749 |
Reaxys-RN | 1813600 |
Chemical Name Translation | 三氟甲磺酸酐 |
LabNetwork Molecule ID | LN00008016 |
InChI | InChI=1S/C2F6O5S2/c3-1(4,5)14(9,10)13-15(11,12)2(6,7)8 |
Signal word |
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GHS Symbol
WGK Germany | 3 |
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;
- S43 In case of fire use ... (indicate in the space the precise type of fire-fighting equipment. If water increases the risk add -?Never use water) 着火时使用(指明具体的消防器材种类,如果用水增加危险,注明“禁止用水”
- S8 Keep container dry 保持容器干燥;
- S30 Never add water to this product 切勿将水加入该产品中;
- S60 This material and its container must be disposed of as hazardous waste 该物质及其容器必须作为危险废物处置;
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Risk Statements | |
- R35 Causes severe burns 会导致严重灼伤
- R14 Reacts violently with water 遇水会猛烈反应
- R22 Harmful if swallowed 吞咽有害
- R40 Limited evidence of a carcinogenic effect 有限证据表明其致癌作用
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Precautionary statements | |
- P303+P361+P353+P310+P363
- P390 Absorb spillage to prevent material damage. 吸收溢出物,防止重大损害。
- P264 Wash hands thoroughly after handling. 处理后要彻底洗净双手。
- P501 Dispose of contents/container to..… 处理内容物/容器.....
- P261 Avoid breathing dust/fume/gas/mist/vapours/spray. 避免吸入粉尘/烟/气体/烟雾/蒸汽/喷雾。
- P305+P351+P338
- 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。
- P301+P330+P331
- P405 Store locked up. 上锁保管。
- P304+P340
- P260 Do not breathe dust/fume/gas/mist/vapours/spray. 不要吸入粉尘/烟/气体/烟雾/蒸汽/喷雾。
- P304+P340+P310
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Hazard statements | |
- H290 May be corrosive to metals 可能腐蚀金属。
- 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
- H351 Suspected of causing cancer 怀疑致癌
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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 |
RTECS | PB2772000 |
Packing Group | II |
UN Number |
UN3265
UN 3265 8/PG 2
3265 |
Storage condition |
Moisture Sensitive
易吸潮,2-8°C密封充氩保存
储存温度2-8℃,充氩保存
Refrigerator
0-10°C
0-10 |
Hazard Codes |
C |
Hazard Class | 8 |
Restrict |
危险品 |
广泛地用于合成烷基和乙烯基三氟甲基磺酸盐。在化工和制药合成中,催化应用于三氟酐、酸和酯。
{ALF} For use in the Vilsmeier formylation of less active substrates, see N,N-Dimethyl­formamide, A13547.
{ALD} Beilstein: 3,IV,35
{ALF} Enolizable carbonyl compounds in the presence of base can be converted to vinyl (enol) triflates: Synthesis, 85 (1982); Org. Synth. Coll., 6, 757 (1988). For conditions employing preferred base, 2,6-Di-tert-butyl-4-methyl­pyridine, L14143, see: Org. Synth. Coll., 8, 97, 126 (1993). Enol triflates behave as a source of vinyl cations. For reviews, see: Angew. Chem. Int. Ed., 17, 333 (1978);
{TRC} Cai, D. et al.: Org. Synth., 10, 112 (2004);
{ALF} Enolizable carbonyl compounds in the presence of base can be converted to vinyl (enol) triflates: Synthesis, 85 (1982); Org. Synth. Coll., 6, 757 (1988). For conditions
{ALF} For formation of keteniminium triflates, see N,N-Dimethyl­acetamide, A10924.
{uni_hamburg} Short: EINECS
{ALF} For a review of chemical transformations induced by the reagent, see: Tetrahedron, 56, 3077 (2000). For a brief feature on uses in synthesis, see: Synlett, 390 (2004).
{ALF} Enolizable carbonyl compounds in the presence of base can be converted to vinyl (enol) triflates: Synthesis, 85 (1982); Org. Synth. Coll., 6, 757 (1988). For conditions employing preferred base, 2,6-Di-tert-butyl-4-methyl­pyridine, L14143, see: Org. Synth. Coll., 8, 9
{ALF} Enolizable carbonyl compounds in the presence of base can be converted to vinyl (enol) triflates: Synthesis, 85 (1982); Org. Synth. Coll., 6, 757 (1988). For conditions employing preferred base, 2,6-Di-tert-butyl-4-methyl­pyridine, L14143, see: Org. Synth. Coll., 8, 97, 126 (1993
{ALF} The Ritter reaction is normally most successful with tertiary alcohols. In contrast, a useful variation allows conversion of primary or secondary alcohols to amides in good yield: Tetrahedron Lett., 30, 581 (1989):
{ALF} Triflic anhydride has also been found to promote the nitration of arenes, even deactivated ones, under mild conditions: Synth