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64329-89-1

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64329-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64329-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,2 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64329-89:
(7*6)+(6*4)+(5*3)+(4*2)+(3*9)+(2*8)+(1*9)=141
141 % 10 = 1
So 64329-89-1 is a valid CAS Registry Number.

64329-89-1Relevant articles and documents

Copper-Photocatalyzed Contra-Thermodynamic Isomerization of Polarized Alkenes

Bouillon, Jean-Philippe,Brégent, Thibaud,Poisson, Thomas

, p. 7688 - 7693 (2020/10/09)

The contra-thermodynamic isomerization of α- and β-substituted cinnamate derivatives catalyzed by the Cu(OAc)2/rac-BINAP complex under blue light irradiation is reported. The use of an oxazolidinone template, which favored the complexation of the copper catalyst to the substrate, allowed the E → Z isomerization of the catalytically formed chromophore under simple and robust reaction conditions in good to excellent ratios. The mechanism of this process based on the transient formation of a chromophore was also studied.

An enantioselective approach to the preparation of chiral sulfones by ir-catalyzed asymmetric hydrogenation

Peters, Byron K.,Zhou, Taigang,Rujirawanich, Janjira,Cadu, Alban,Singh, Thishana,Rabten, Wangchuk,Kerdphon, Sutthichat,Andersson, Pher G.

, p. 16557 - 16562 (2015/01/09)

Several chiral sulfonyl compounds were prepared using the iridium catalyzed asymmetric hydrogenation reaction. Vinylic, allylic and homoallylic sulfone substitutions were investigated, and high enantioselectivity is maintained regardless of the location of the olefin with respect to the sulfone. Impressive stereoselectivity was obtained for dialkyl substitutions, which typically are challenging substrates in the hydrogenation. As expected, the more bulky Z-substrates were hydrogenated slower than the corresponding E isomers, and in slightly lower enantioselectivity.

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