Cas 638204-29-2,Sm(3+)*((C6H2(C4H9)2O)CH2N(CH3)(C6H3(CH3)))2(2-)*N(Si(CH3)2H)2(1-) = SmC50H76N3O2Si2

638204-29-2

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Basic information

Product Name: Sm⁽³⁺⁾*((C₆H₂(C₄H₉)2O)CH₂N(CH₃)(C₆H₃(CH₃)))2^(2-)*N(Si(CH₃)2H)2^(1-) = SmC₅₀H₇₆N₃O₂Si₂
Synonyms:
CAS NO:638204-29-2
Molecular Formula:
Molecular Weight: 957.703
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Sm⁽³⁺⁾*((C₆H₂(C₄H₉)2O)CH₂N(CH₃)(C₆H₃(CH₃)))2^(2-)*N(Si(CH₃)2H)2^(1-) = SmC₅₀H₇₆N₃O₂Si₂(CAS DataBase Reference)
NIST Chemistry Reference: Sm⁽³⁺⁾*((C₆H₂(C₄H₉)2O)CH₂N(CH₃)(C₆H₃(CH₃)))2^(2-)*N(Si(CH₃)2H)2^(1-) = SmC₅₀H₇₆N₃O₂Si₂(638204-29-2)
EPA Substance Registry System: Sm⁽³⁺⁾*((C₆H₂(C₄H₉)2O)CH₂N(CH₃)(C₆H₃(CH₃)))2^(2-)*N(Si(CH₃)2H)2^(1-) = SmC₅₀H₇₆N₃O₂Si₂(638204-29-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 638204-29-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 638204-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,8,2,0 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 638204-29:
(8*6)+(7*3)+(6*8)+(5*2)+(4*0)+(3*4)+(2*2)+(1*9)=152
152 % 10 = 2
So 638204-29-2 is a valid CAS Registry Number.

638204-29-2Upstream product

637743-50-1 ((C₆H₂(C(CH₃)3)2OH)CH₂N(CH₃)(C₆H₃(CH₃)))2

638204-29-2Downstream Products

638204-29-2Relevant academic research and scientific papers

Chiral-at-metal organolanthanides: Enantioselective aminoalkene hydroamination/cyclisation with non-cyclopentadienyls

O'Shaughnessy, Paul N.,Knight, Paul D.,Morton, Colin,Gillespie, Kevin M.,Scott, Peter

, p. 1770 - 1771 (2003)

Chiral non-racemic complexes [ML{N(SiMe2H)2}(thf)] (M = Y, La, H2L = salicylaldimine ligands derived from 2,2′-diamino-6,6′-dimethylbiphenyl) are found not to be effective catalysts for the intramolecular hydroamination of

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