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1-Hepten-4-ol, 7-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-iodo-, (4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

481048-35-5

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481048-35-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 481048-35-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,1,0,4 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 481048-35:
(8*4)+(7*8)+(6*1)+(5*0)+(4*4)+(3*8)+(2*3)+(1*5)=145
145 % 10 = 5
So 481048-35-5 is a valid CAS Registry Number.

481048-35-5Downstream Products

481048-35-5Relevant academic research and scientific papers

New syntheses of E7389 C14-C35 and halichondrin C14-C38 building blocks: Double-inversion approach

Kim, Dae-Shik,Dong, Cheng-Guo,Kim, Joseph T.,Guo, Haibing,Huang, Jian,Tiseni, Paolo S.,Kishi, Yoshito

supporting information; scheme or table, p. 15636 - 15641 (2010/01/30)

With sequential use of catalytic asymmetric Cr-mediated coupling reactions, E7389 C14-C35 and halichondrin C14-C38 building blocks have been stereoselectively synthesized. The C19-C20 bond is first formed via the catalytic asymmetric Ni/Cr-mediated coupli

Further improvement on sulfonamide-based ligand for catalytic asymmetric 2-haloallylation and allylation

Zhang, Zhiyu,Huang, Jian,Ma, Bin,Kishi, Yoshito

supporting information; experimental part, p. 3073 - 3076 (2009/05/11)

(Chemical Equation Presented) The sulfonamide-based ligand B was found to exhibit an outstanding crystallinity and perform well as a ligand for Cr-mediated catalytic asymmetric 2-haloallylation and allylation. The new ligand has an appealing advantage ove

Fe/Cr- and Co/Cr-mediated catalytic asymmetric 2-haloallylations of aldehydes

Kurosu, Michio,Lin, Mei-Huey,Kishi, Yoshito

, p. 12248 - 12249 (2007/10/03)

The first example to couple aldehydes and 3-bromo-2-halopropenes in a catalytic asymmetric manner is reported. The coupling reaction is effected by the use of a chiral sulfonamide-Cr complex (prepared in situ from 1d, CrBr3, Fe(III) or from Co(II), Et3N, and Mn), TMSCl, and 2,6-lutidine. The method reported here is operationally simple and scalable, furnishing 3-halohomoallylic alcohols with a synthetically useful level of enantiomeric excess. Copyright

New catalytic cycle for couplings of aldehydes with organochromium reagents

Namba, Kosuke,Kishi, Yoshito

, p. 5031 - 5033 (2007/10/03)

(Chemical Equation Presented) A new catalytic cycle has been developed to effect all three subgroups of Cr-mediated couplings, i.e., (1) Ni/Cr-mediated alkenylation, alkynylation, and arylation, (2) Co/Cr-mediated 2-haloallylation, alkylation, and proparg

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