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(R)-2-Benzyloxycarbonylamino-3-((R)-2-benzyloxycarbonylamino-2-methoxycarbonyl-ethylsulfanylmethylsulfanyl)-propionic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

226899-29-2

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226899-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226899-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,8,9 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 226899-29:
(8*2)+(7*2)+(6*6)+(5*8)+(4*9)+(3*9)+(2*2)+(1*9)=182
182 % 10 = 2
So 226899-29-2 is a valid CAS Registry Number.

226899-29-2Downstream Products

226899-29-2Relevant academic research and scientific papers

Asymmetric induction through metalation of chiral dithioacetals and oxathioacetals

Zaidi, Javid H.,Gunjial, Naseem Iqbal

, p. 2835 - 2845 (2008/03/11)

The work presented in this article consists of synthesis of chiral dithioacetals and oxathioacetals using pure chiral auxiliaries, such as, (+) camphor, (-) menthol, and L-cysteine. Metalation of these chiral dithioacetals and oxathioacetals, followed by nucleophilic addition to benzaldehyde and removal of chiral auxiliary, furnished scalemic mandelic acid with various enantiomeric purities. Copyright Taylor & Francis Group, LLC.

A new efficient method for S-CH2-S bond formation and its application to a djenkolic acid-containing cyclic enkephalin analog

Ueki, Masaaki,Ikeo, Takayoshi,Hokari, Kumiko,Nakamura, Keiko,Saeki, Akihiko,Komatsu, Hiroshi

, p. 829 - 838 (2007/10/03)

An efficient methylene insertion reaction to construct an S-CH2-S bridge between two cysteine residues occurred when the thiol-protecting dimethylphosphinothioyl (Mpt) group of Z-Cys(Mpt)-OMe was removed with tetrabutylammonium fluoride hydrate in CH2Cl2. The thiol-free form gave similar results, albeit the yields were somewhat lower. In both cases, the best yields were obtained using 2 molar amounts of the reagent. Higher amounts of the reagent reduced the yield because of dehydroalanine formation. In the case of penicillamine, the thiol-free form was better in reactivity than the S-Mpt form, which required double the amount of the reagent to give the same yield. The reaction was successfully used in a synthesis of a cyclic enkephalin analog with the S-CH2-S bridge.

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