Chemical Name | Tin(II) Trifluoromethanesulfonate |
Alfabeta Name | TINTRIFLUOROMETHANESULFONATE |
Synonym |
Sn(OTf)2 三氟甲烷磺酸锡(II) 三氟甲磺酸锡 |
PubChem Substance ID | 87576975 |
Reaxys-RN | 11552396 |
Chemical Name Translation | 三氟甲烷磺酸锡 |
MDL Number | MFCD00191251 |
CAS Number | 62086-04-8 |
LabNetwork Molecule ID | LN00117898 |
Warnings |
IRRITANT |
Safety Statements | |
- S9 Keep container in a well-ventilated place 保持容器在通风良好的场所;
- 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;
- S36/37 Wear suitable protective clothing and gloves 穿戴适当的防护服和手套;
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Packing Group | III |
UN Number |
UN3288
3146 |
Risk Statements | |
|
Storage condition |
Moisture Sensitive
0-10
冷库贮存。
0-10°C |
WGK Germany | 3 |
GHS Symbol
Precautionary statements | |
- 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。
- P403+P233
- P261 Avoid breathing dust/fume/gas/mist/vapours/spray. 避免吸入粉尘/烟/气体/烟雾/蒸汽/喷雾。
- P264 Wash hands thoroughly after handling. 处理后要彻底洗净双手。
- P271 Use only outdoors or in a well-ventilated area.? 只能在室外或通风良好的地方使用。
- P312 Call a POISON CENTER or doctor/physician if you feel unwell. 如果你感觉不适,呼叫解毒中心或医生/医师。
- P301+P310+P330
- P332+P313
- P302+P352+P312+P361+P364
- P501 Dispose of contents/container to..… 处理内容物/容器.....
- P405 Store locked up. 上锁保管。
- P305+P351+P338+P337+P313
- P304+P340+P311
- P270 Do not eat, drink or smoke when using this product. 使用本产品时不要吃东西,喝水或吸烟。
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Signal word |
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Hazard statements | |
- H301+H311+H331
- 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 |
Hazard Codes |
C |
Hazard Class | 6.1 |
{ALF} Promotes glycosidation reactions, e.g. of acetobromoglucose to give, stereoselectively, ß-glucosides: Tetrahedron Lett., 26, 1713 (1985). Also used in a variety of other glycosidation reactions; see, e.g.: Tetrahedron Lett., 28, 5041 (1987); Chem. Lett., 1123 (1996); Liebigs Ann. Chem., 1623 (1996); Tetrahedron, 52, 3897 (1996); Eur. J. Org. Chem., 1423 (2000).
{ALF} Can transfer an allyl group from a homoallylic alcohol to an aldehyde: J. Am. Chem. Soc., 120, 6609 (1998); 122, 1310 (2000).
{ALF} In combination with a base (e.g. DBU), promotes the addition of 1-alkynes to carbonyl groups to give alkynols: J. Org. Chem., 56, 4091 (1991).
{ALF} Catalyzes electrophilic sulfonylation of aromatic rings by sulfonyl chlorides, generally in good yields: Tetrahedron, 57, 241 (2001).
{ALF} Versatile mild Lewis acid catalyst.
{ALF} Introduced by Mukaiyama to promote aldol-type reactions via tin enolates, either stoichiometrically: Tetrahedron, 40, 1381 (1984), or catalytically: Tetrahedron, 45, 1197 (1989). In the presence of a chiral amine, the reaction is enantioselective: Chem. Lett., 1209 (1991); J. Am. Chem. Soc., 113, 4247 (1991). For further discussion of this and other reactions of tin enolates, see: Encyclopedia of Reagents for Organic Synthesis, L. A. Paquette, Ed., Wiley, Chichester (1995), vol. 7, p. 4907.
{ALF} Reagent for selective deprotection of N-Boc groups: Synth. Commun., 33, 445 (2003).