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CAS RN: 546-67-8 | 제품번호: L0021
Lead Tetraacetate (contains Acetic Acid)
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•보관 조건은 예고없이 변경 될 수 있습니다. 제품 보관 조건의 최신 자료는 홈페이지에 기재되어 있으니 양해 부탁드립니다.
•본건의 원가격은 한국 대리점의 예상 판매가격입니다.자세한 정보가 필요하시면 연락해 주십시오.(SEJIN CI Co., Ltd. (한국총대리점) 전화 : 02-2655-2480 이메일 : sales@sejinci.co.kr)
•보관 조건은 예고없이 변경 될 수 있습니다. 제품 보관 조건의 최신 자료는 홈페이지에 기재되어 있으니 양해 부탁드립니다.
제품번호 | L0021 |
Purity/Analysis Method | >96.0%(T) |
M.F. / M.W. | C__8H__1__2O__8Pb = 443.38 |
물리적 상태 (20 ℃) | Solid |
보관 조건 | Refrigerated (0-10°C) |
불활성 가스 하에서 보관 | Store under inert gas |
피해야 할 조건 | Air Sensitive,Moisture Sensitive,Heat Sensitive |
CAS RN | 546-67-8 |
Reaxys-RN | 3595640 |
PubChem Substance ID | 87571991 |
Merck Index (14) | 5423 |
MDL 번호 | MFCD00008693 |
규격표
Appearance | White to Almost white powder to crystal |
Purity(Iodometric Titration) | min. 96.0 % |
NMR | confirm to structure |
물성치(참고치)
mp | 180 °C |
용해성 (용해) | Nitrobenzene, Benzene, Chloroform, Alcohol |
GHS
픽토그램 | |
신호 워드 | Danger |
위험물 및 유해 등록 | H302 + H332 : Harmful if swallowed or if inhaled. H315 : Causes skin irritation. H361 : Suspected of damaging fertility or the unborn child. H373 : May cause damage to organs through prolonged or repeated exposure. H341 : Suspected of causing genetic defects. H350 : May cause cancer. H272 : May intensify fire; oxidizer. |
주의 사항 | P501 : Dispose of contents/ container to an approved waste disposal plant. P260 : Do not breathe dust/ fume/ gas/ mist/ vapors/ spray. P270 : Do not eat, drink or smoke when using this product. P202 : Do not handle until all safety precautions have been read and understood. P220 : Keep/Store away from clothing/ combustible materials. P210 : Keep away from heat. P201 : Obtain special instructions before use. P221 : Take any precaution to avoid mixing with combustibles. P271 : Use only outdoors or in a well-ventilated area. P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P370 + P378 : In case of fire: Use dry sand, dry chemical or alcohol-resistant foam to extinguish. P308 + P313 : IF exposed or concerned: Get medical advice/ attention. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. P301 + P312 + P330 : IF SWALLOWED: Call a POISON CENTER/doctor if you feel unwell. Rinse mouth. P304 + P340 + P312 : IF INHALED: Remove person to fresh air and keep comfortable for breathing. Call a POISON CENTER/doctor if you feel unwell. P405 : Store locked up. |
법규 정보
RTECS # | AI5300000 |
운송 정보
UN 번호 | UN3087 |
등급 | 5.1 / 6.1 |
포장 그룹 | III |
HS 번호* | 2915.29-000 |
Application
Generation of Benzyne using Pb(OAc)4 and Synthesis of Dibenzocyclobutadiene
Reference
- Reactivity of Dehydrometallophthalocyanines and -porphyrazines
Application
Oxidation of 1,2-Diols (Criegee Oxidation)1)
Typical Procedure:
To a solution of olefine 1 (11.9 mg, 0.030 mmol) and DMAP (7.33 mg, 0.060 mmol, 2 eq.) in t-BuOH (100 µL) is added a solution of OsO4 (7.62 mg, 0.030 mmol, 1 eq.) in water (200 µL). The orange-red solution is stirred at rt for 5-10 min. Solid Na2SO3 (19 mg, 0.15 mmol, 5 eq.) is added. The resulting mixture is applied directly to preparative TLC (CHCl3 : MeOH : NH4OH = 25 : 10 : 1) and diol is collected by washing silica gel with a mixture of CHCl3 : MeOH = 2 : 1. Concentration under reduced pressure (< 25 ℃) affords the slightly unstable diol 2, which is dissolved in CH2Cl2 (2 mL). The solution then is cooled to -20 ℃ and AcOH (9.0 mg, 8.6 µL, 5 eq.) is added, followed by solid Pb(OAc)4 (11 mg, 0.025 mmol) in portions. TLC (CH2Cl2 : MeOH = 1 : 1 and 25 : 1) monitors the end of the reaction. The resulting yellow solution is stirred at -20 ℃ for 5-10 min, washed with water, saturated NaHCO3 and brine, dried over Na2SO4 and evaporated under reduced pressure to give 3 (8.5 mg, Y. 71%) of silica gel labile ketone as a yellow powder.
To a solution of olefine 1 (11.9 mg, 0.030 mmol) and DMAP (7.33 mg, 0.060 mmol, 2 eq.) in t-BuOH (100 µL) is added a solution of OsO4 (7.62 mg, 0.030 mmol, 1 eq.) in water (200 µL). The orange-red solution is stirred at rt for 5-10 min. Solid Na2SO3 (19 mg, 0.15 mmol, 5 eq.) is added. The resulting mixture is applied directly to preparative TLC (CHCl3 : MeOH : NH4OH = 25 : 10 : 1) and diol is collected by washing silica gel with a mixture of CHCl3 : MeOH = 2 : 1. Concentration under reduced pressure (< 25 ℃) affords the slightly unstable diol 2, which is dissolved in CH2Cl2 (2 mL). The solution then is cooled to -20 ℃ and AcOH (9.0 mg, 8.6 µL, 5 eq.) is added, followed by solid Pb(OAc)4 (11 mg, 0.025 mmol) in portions. TLC (CH2Cl2 : MeOH = 1 : 1 and 25 : 1) monitors the end of the reaction. The resulting yellow solution is stirred at -20 ℃ for 5-10 min, washed with water, saturated NaHCO3 and brine, dried over Na2SO4 and evaporated under reduced pressure to give 3 (8.5 mg, Y. 71%) of silica gel labile ketone as a yellow powder.
References
- 1)Eine oxydative spaltung von glykolen (II. Mitteil. über oxydationen mit blei(IV)-salzen)
- 2)Enantioselective total synthesis of aspidophytine
PubMed Literature
기사 / 브로셔
TCIMail
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