Basic Information |
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Product Name: | BIS(1,5-CYCLOOCTADIENE)NICKEL(0) |
CAS: | 1295-35-8 |
English Synonyms: | NICKEL(COD)2 ; CYCLOOCTA-1,5-DIENE, NICKEL ; NI(COD)2 ; BIS(CYCLOOCTADIENE)NICKEL ; BIS(1,5-CYCLOOCTADIENE)NICKEL ; BIS(1,5-CYCLOOCTADIENE)NICKEL(0) |
MDL Number.: | MFCD00058902 |
H bond acceptor: | 0 |
H bond donor: | 0 |
Smile: | C/1C/C=C\CC/C=C1.C/1C/C=C\CC/C=C1.[Ni] |
InChi: | InChI=1S/2C8H12.Ni/c2*1-2-4-6-8-7-5-3-1;/h2*1-2,7-8H,3-6H2;/b2*2-1-,8-7-; |
InChiKey: | InChIKey=JRTIUDXYIUKIIE-KZUMESAESA-N |
Property |
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Melting Point: | 60 DEG C (DEC)(LIT)/60 °C |
Comments: | APPLICATION: CATALYST FOR THE CYCLOADDITION OF 1,3-DIENES APPLICATION: REACTANT FOR: OXIDATIVE ADDITION REACTIONS. CATALYST FOR: ASYMMETRIC ALPHA-ARYLATION AND HETEROARYLATION OF KETONES WITH CHLOROARENES. CROSS-COUPLING REACTIONS. REGIOSELECTIVE AND STEREOSELECTIVE CARBOXYLATION/CYCLIZATION OF ALLENYL ALDEHYDES UNDER A CARBON DIOXIDE ATMOSPHERE. METHYL CARBOXYLATION OF HOMOPROPARGYLIC ALCOHOLS. STEREOSELECTIVE BORYLATIVE KETONE-DIENE COUPLING. CYCLOADDITION OF BENZAMIDES WITH INTERNAL ALKYNES APPLICATION: USED TO CATALYZE THE ADDITION OF ALLYL PHENYL SULFIDE TO ALKYNES LEADING TO 1,4-DIENES. THE REACTION WITH TERMINAL ACETYLENES PROCEEDS IN HIGH YIELD AND HIGH SELECTIVITY. A VARIETY OF FUNCTIONAL GROUPS ARE TOLERATED RIDADR: UN 1325 4.1/PG 2 RTECS: QR6135000 STORAGE TEMPERATURE: -20 DEG C UNSPSC: 12352103 WGK: 3 |
Safety information |
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Symbol: | GHS02 GHS08 |
Signal word: | Danger |
Hazard statements: | H228-H334-H351 |
Precautionary statements: | P210-P261-P281-P342 + P311 |
hazard symbol: | F,Xn |
Risk Code: | R:11-40 |
Safe Code: | S:36/37 |
WGK Germany: | 3 |
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