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Carbamic acid, [(1R)-1-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2,2-dimethoxyprop yl]-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

161150-58-9

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161150-58-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161150-58-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,1,5 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 161150-58:
(8*1)+(7*6)+(6*1)+(5*1)+(4*5)+(3*0)+(2*5)+(1*8)=99
99 % 10 = 9
So 161150-58-9 is a valid CAS Registry Number.

161150-58-9Downstream Products

161150-58-9Relevant academic research and scientific papers

Synthesis of functional "top-half" partial structures of azinomycin A and B

Coleman, Robert S.,Tierney, Mark T.,Cortright, Sarah B.,Carper, Daniel J.

, p. 7726 - 7735 (2008/02/12)

(Chemical Equation Presented) The design and synthesis of a detailed series of functional "top-half substructures of azinomycin A and B is described.

Synthetic studies of carzinophilin. Part 2: Synthesis of 3,4-dibenzyloxy-2-methylidene-1-azabicyclo[3.1.0]hexane systems corresponding to the C1-C17 fragment of carzinophilin

Hashimoto, Masaru,Matsumoto, Miyoko,Terashima, Shiro

, p. 3041 - 3062 (2007/10/03)

A model compound bearing the C1-C17 fragment of carzinophilin was synthesized. The synthesis involved coupling reaction of a cyclic thioimidate with the 4H-oxazol-5-one derivative, ring-opening of the 4H-oxazol-5-one to furnish a dehydropeptide system, elaboration of the C1-C6 enolamide, and construction of the aziridine ring as key steps.

A Novel Synthesis of the C1-C17 Fragment of Carzinophilin

Hashimoto, Masaru,Terashima, Shiro

, p. 9409 - 9412 (2007/10/02)

The title synthesis was achieved by featuring i) condensation of the 2-methylthio-Δ1-pyrroline (C8-C13 moiety) with the Δ2-oxazolin-5-one (C6,C7,N16, and C17 moiety), ii) activation of the Δ2-oxazolin-5-one system toward n

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