Chemical Name | Palladium(II) acetate |
Synonym |
Palladium (II) acetate
{LY} Palladium (II) acetate
{} {LY} Palladium (II) acetate
{} {} {LY} Palladium (II) acetate
{} {} {} {LY} Palladium (II) acetate
{} {} {} {} {LY} Palladium (II) acetate
{} {} {} {} {} {LY} Palladium (II) acetate
{} {} {} {} {} {} {LY} Palladium (II) acetate
{} {} {} {} {} {} {} {LY} Palladium (II) acetate
{} {} {} {} {} {} {} {} {LY} Palladium (II) acetate
{} {} {} {} {} {} {} {} {}
{} {} {} {} {} {} {} {} {} {LY} Palladium (II) acetate
{} {} {} {} {} {} {} {} {} {} {LY} Palladium (II) acetate
{} {} {} {} {} {} {} {} {} {} {} {LY} Palladium (II) acetate
{} {} {} {} {} {} {} {} {} {} {} {} {
{} {} {} {} {} {} {} {} {} {} {} {} {LY} Palladium (II) acetate
{} {} {} {} {} {} {} {} {} {} {} {} {} {LY} Palladium (II) acetate
{} {} {} {} {} {} {} {} {} {} {} {} {} {}
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} Palladium (II) acetate
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} Palladium (II) acetate
{} {} {} {} {} {} {} {} {} {} {} {} |
Beilstein Registry Number | 6086766 |
PubChem Substance ID | 167845 |
CAS Number | 3375-31-3 |
EC Number | 222-164-4 |
MDL Number | MFCD00012453 |
Reaxys-RN | 3375313 |
Merck Number | 6991 |
Chemical Name Translation | 乙酸钯(Ⅱ) |
LabNetwork Molecule ID | LN00193292 |
InChI | InChI=1S/2C2H4O2.Pd/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2 |
Canonical SMILES | C[Pd]C.O=C=O.O=C=O |
Precautionary statements | |
- P305+P351+P338+P310
- 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。
- P264 Wash hands thoroughly after handling. 处理后要彻底洗净双手。
- 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
- 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。
- P310 Immediately call a POISON CENTER or doctor/physician. 立即呼救解毒中心或医生/医师。
- P301+P330+P331
- P337+P313
|
WGK Germany | 2 |
GHS Symbol
Signal word |
Danger |
Hazard statements | |
- H351 Suspected of causing cancer 怀疑致癌
- H318 Causes serious eye damage 严重伤害眼睛
- H314 Causes severe skin burns and eye damage 导致严重的皮肤灼伤和眼睛损伤
- H361d Suspected of damaging the unborn child 怀疑对未出生婴儿造成伤害
- H303 May be harmfully swallowed 吞食可能有害
|
Hazard Codes |
C
8
Xn
Xi
Xi,Xn |
RTECS | AJ1900000 |
Personal Protective Equipment |
dust mask type N95 (US), Eyeshields, Gloves |
Safety Statements | |
- 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);
- S24 Avoid contact with skin 避免皮肤接触;
- S37/39 Wear suitable gloves and eye/face protection 穿戴适当的手套和眼睛/面保护;
- 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;
- S61 Avoid release to the environment. Refer to special instructions/safety data sheet 避免释放到环境中,参考特别指示/安全收据说明书;
- S39 Wear eye/face protection 戴眼睛/面孔保护装置;
- S36 Wear suitable protective clothing 穿戴适当的防护服;
|
Risk Statements | |
- R41 Risk of serious damage to eyes 有严重损伤眼睛的危险
- R43 May cause sensitisation by skin contact 皮肤接触会产生过敏反应
- R53 May cause long-term adverse effects in the aquatic environment 对水生环境有长期的有害作用
- R35 Causes severe burns 会导致严重灼伤
- R36/37/38 Irritating to eyes, respiratory system and skin 对眼睛、呼吸系统和皮肤有刺激性
- R40 Limited evidence of a carcinogenic effect 有限证据表明其致癌作用
|
Packing Group | Ⅲ |
UN Number |
|
Storage condition |
2-8°C, protect from light, stored under nitrogen
{LY} 2-8°C, protect from light, stored under nitrogen
Store at R.T.
{} {LY} 2-8°C, protect from light, stored under nitrogen
{} {} {LY} 2-8°C, protect from light, stored under nitrogen
{} {} {} {LY} 2-8°C, protect from light, stored under nitrogen
{} {} {} {} {LY} 2-8°C, protect from light, stored under nitrogen
{} {} {} {} {} {LY} 2-8°C, protect from light, stored under nitrogen
{} {} {} {} {} {} {LY} 2-8°C, protect from light, stored under nitrogen
{} {} {} {} {} {} {} {LY} 2-8°C, protect from light, stored under nitrogen
{} {} {} {} {} {} {} {} {LY} 2-8°C, protect from light, stored under nitrogen
{} {} {} {} {} {} {} {} {} {LY} 2-8°C, protect from light, stored under nitrogen
{} {} {} {} {} {} {} {} {} {} {LY} 2-8°C, protect from light, stored under nitrogen
{} {} {} {} {} {} {} {} {} {} {} {LY} 2-8°C, protect from light, stored under nitrogen
{} {} {} {} {} {} {} {} {} {} {} {} {LY} 2-8°C, protect |
TYPE OF TEST : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE : Oral
SPECIES OBSERVED : Rodent - mouse
DOSE/DURATION : 2100 mg/kg
TOXIC EFFECTS :
Behavioral - somnolence (general depressed activity)
Lungs, Thorax, or Respiration - dyspnea
Gastrointestinal - ulceration or bleeding from stomach
REFERENCE :
GISAAA Gigiena i Sanitariya. For English translation, see HYSAAV. (V/O
Mezhdunarodnaya Kniga, 113095 Moscow, USSR) V.1- 1936-
Volume(issue)/page/year: 51(12),88,1986
A catalyst for intramolecular coupling.
{ALF} For a brief feature on uses of palladium acetate in synthesis, see: Synlett, 329 (2006).
{ALF}
{ALF} For the Heck-type reaction of arenediazonium salts with alkenes, see p-Anisidine, A10946.
{ALF} Use in an improved "Wacker" oxidation of terminal alkenes to 2-alkanones, with p-Benzoquinone, A13162, as the co-oxidant, gives rates up to 50 times higher than earlier procedures: J. Org. Chem., 55, 2924 (1990).
{ALFA} Use in an improved "Wacker" oxidation of terminal alkenes to 2-alkanones, with p-Benzoquinone, A13162, as the co-oxidant, gives rates up to 50 times higher than earlier procedures: J. O
{ALF} Also catalyzes the allylic acetoxylation of cycloalkenes: Org. Synth. Coll., 8, 137 (1993).
{ALF} Widely used as catalyst, in the presence of a phosphine ligand and a base, in the Heck (or Mizoroki-Heck) reaction, for coupling of aryl or vinyl halides with alkenes. Reviews: Org. React., 27, 345 (1982); Acc. Chem. Res., 12, 146 (1979); 28, 2 (1995); Angew. Chem. Int. Ed., 33, 2379 (1994); Chem. Rev., 100, 3009 (2000). In many reactions, e.g. the arylation of ɑß-unsaturated esters, Tri(o-tolyl)­phosphine, A12093 is superior to triphenylphosphine: J. Org. Chem., 43, 2952 (1978).
{ALF} For catalysis of the efficient "ligandless" Suzuki cross-coupling of arylboronic acids with aryl iodides, see: J. Org. Chem., 59, 5034 (1994); Org. Synth., 75, 61 (1997).
{ALF} In the presence of TBAB, catalyzes direct homocoupling of aryl halides: Tetrahedron Lett., 39, 2559 (1998).
{ALF} o-Allylic or o-vinylic phenols undergo phosphine-free Pd-catalyzed cross-coupling with vinylic halides and triflates, giving dihydrobenzopyrans and dihydrobenzofurans respectively: Tetrahedron Lett., 39, 237 (1998):
{ALF} Use in a