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Silane, (1,1-dimethylethyl)dimethyl[(1S)-1-[[(2S,5R)-tetrahydro-5-[(1S)-1-methyl -2-(phenylmethoxy)ethyl]-2-furanyl]methyl]butoxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

406673-94-7

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406673-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 406673-94-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,6,7 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 406673-94:
(8*4)+(7*0)+(6*6)+(5*6)+(4*7)+(3*3)+(2*9)+(1*4)=157
157 % 10 = 7
So 406673-94-7 is a valid CAS Registry Number.

406673-94-7Downstream Products

406673-94-7Relevant academic research and scientific papers

Synthesis of the L-acid (C1-C18) fragment of pamamycin-593 and De-N-methylpamamycin-579

Miura, Ayako,Takigawa, Shin-Ya,Furuya, Yukito,Yokoo, Yusuke,Kuwahara, Shigefumi,Kiyota, Hiromasa

experimental part, p. 4955 - 4962 (2009/06/06)

The L-acid (C1-C18) fragment of pamamycin-593 and de-N-methylpamamycin-579, strong aerial mycelium-inducers of Streptomyces alboniger, was synthesized using a cis-selective iodoetherification and a nucleophilic addition of a cerium acetylide to an aldehyde as the key steps. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

Synthesis of southern (C1′-C11′) and eastern (C8-C18) fragments of pamamycin-607, an aerial mycelium-inducing substance of Streptomyces alboniger

Kiyota, Hiromasa,Furuya, Yukito,Kuwahara, Shigefumi,Oritani, Takayuki

, p. 2630 - 2637 (2007/10/03)

Synthesis of the southern C1′-C11′ and eastern C8-C18 fragments of pamamycin-607, an aerial mycelium-inducing substance of Streptomyces alboniger, was achieved. The southern fragment was synthesized by using the Evans aldol reaction and cis-selective iodoetherification as the key steps in a 9.6% overall yield (7 steps). The eastern fragment was constructed via the Julia coupling reaction and cis-selective iodoetherification in a 3.0% overall yield (8 steps from the known epoxide).

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