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tert-butyl((2S,3S,4R,5S,E)-3,5-dimethoxy-2,4-dimethyl-7-phenylhept-6-enyloxy)diphenylsilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

307492-70-2

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307492-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 307492-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,7,4,9 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 307492-70:
(8*3)+(7*0)+(6*7)+(5*4)+(4*9)+(3*2)+(2*7)+(1*0)=142
142 % 10 = 2
So 307492-70-2 is a valid CAS Registry Number.

307492-70-2Relevant academic research and scientific papers

Step-economic synthesis of (+)-crocacin C: A concise crotylboronation/[3,3] -sigmatropic rearrangement approach

Pasqua, Adele E.,Ferrari, Frank D.,Hamman, Chris,Liu, Yanzhou,Crawford, James J.,Marquez, Rodolfo

experimental part, p. 6989 - 6997 (2012/09/25)

The step-economic total synthesis of (+)-crocacin C has been achieved in 20% yield from commercially available starting materials. This approach requires the isolation of only 8 intermediates and can provide a reliable supply of (+)-crocacin C for the development of new antifungal and crop protection agents.

Total synthesis of (+)-crocacin C

Sirasani, Gopal,Paul, Tapas,Andrade, Rodrigo B.

scheme or table, p. 3648 - 3655 (2010/08/03)

Two approaches toward the total synthesis of cytotoxic polyketide natural product (+)-crocacin C (1) are described. The first approach, which was ultimately unsuccessful, was replaced altogether with a second that afforded target 1 in 10 linear steps from commercially available Evans' chiral propionimide (5% overall yield). No protecting groups were utilized in the total synthesis of 1.

Asymmetric total synthesis of the myxobacteria metabolites crocacins A-D

Feutrill, John T.,Lilly, Michael J.,White, Jonathan M.,Rizzacasa, Mark A.

, p. 4880 - 4895 (2008/09/21)

The total syntheses of crocacins A-D are described. The key steps were a syn-aldol reaction followed by anti-reduction to secure the stereotetrad and acylation of an ene- or dienecarbamate to form the enamide. Crown Copyright

Total synthesis of (+)-crocacin D

Dias, Luiz C.,De Oliveira, Luciana G.,Vilcachagua, Janaina D.,Nigsch, Florian

, p. 2225 - 2234 (2007/10/03)

(Chemical Equation Presented) The total synthesis of (+)-crocacin D is described. The convergent asymmetric synthesis relies on the use of a Stille cross-coupling between an (E)-vinyl stannane with an (E)-vinyl iodide to establish the (E,E)-dienamide moie

Total synthesis of (+)-crocacin C

Dias, Luiz C.,De Oliveira, Luciana G.

, p. 3951 - 3953 (2007/10/03)

equation presented The total synthesis of (+)-crocacin C is described. The convergent asymmetric synthesis relies on the use of a regio- and diastereoselective epoxidation of an allylic alcohol with m-CPBA followed by epoxide opening with Me2Cu

Total synthesis of (+)-crocacin C.

Feutrill,Lilly,Rizzacasa

, p. 3365 - 3367 (2007/10/03)

The first asymmetric synthesis of (+)-crocacin C (3) is described which served to confirm the absolute configuration of this compound. The key step in the sequence was the stereoselective assembly of the (E,E)-diene amide side chain by a Stille cross-coup

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