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(1S)-1-(4-methoxy-phenyl)-1,5-anhydro-D-mannitol is a complex organic compound with the molecular formula C11H14O6. It is a chiral molecule, denoted by the (1S) configuration, which refers to the spatial arrangement of atoms around the chiral center. (1S)-1-(4-methoxy-phenyl)-1,5-anhydro-D-mannitol features a 4-methoxy-phenyl group attached to a 1,5-anhydro-D-mannitol moiety. The 1,5-anhydro-D-mannitol part of the molecule is a derivative of D-mannitol, a sugar alcohol, with the hydroxyl groups at the 1 and 5 positions removed, forming a double bond. The 4-methoxy-phenyl group adds a methoxy (-OCH3) substituent to a phenyl ring, which is attached to the 1-position of the anhydro-D-mannitol. (1S)-1-(4-methoxy-phenyl)-1,5-anhydro-D-mannitol is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structure and functional groups.

28538-11-6

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28538-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28538-11-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,3 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 28538-11:
(7*2)+(6*8)+(5*5)+(4*3)+(3*8)+(2*1)+(1*1)=126
126 % 10 = 6
So 28538-11-6 is a valid CAS Registry Number.

28538-11-6Relevant academic research and scientific papers

Cyanide-Free Synthesis of Glycosyl Carboxylic Acids and Application for the Synthesis of Scleropentaside A

Zou, Liang-Jing,Pan, Qiang,Li, Cai-Yi,Zhang, Ze-Ting,Zhang, Xiao-Wei,Hu, Xiang-Guo

supporting information, p. 8302 - 8306 (2020/11/18)

We have developed a cyanide-free strategy for the synthesis of glycosyl carboxylic acids, which can provide 1,2-trans or 1,2-cis glycosyl carboxylic acids and is compatible with common protecting groups. The synthetic utility was demonstrated by the synth

Aryl-β-C-glucosidation using glucal boronate: Application to the synthesis of tri-O-methylnorbergenin

Sakamaki, Shigeki,Kawanishi, Eiji,Nomura, Sumihiro,Ishikawa, Tsutomu

, p. 5744 - 5753 (2012/09/08)

Novel aryl-β-C-glucosidation method using glucal boronate was developed. This protocol can offer several advantages including use of non-toxic, easily handling glucal boronate as a crystalline solid and storable at room temperature for several months. Tri-O-methylnorbergenin (8,10-di-O-methylbergenin), an anti-HIV active bergenin derivative, was concisely synthesized by application of the aryl-β-C-glucosidation method.

Triisobutylaluminium (TIBAL) promoted rearrangement of C-glycosides

Sollogoub, Matthieu,Sinay, Pierre

, p. 843 - 858 (2007/10/03)

Triisobutylaluminium-promoted rearrangement of unsaturated glycosides containing electron-donating aglycons, such as C-aryl glycosides, provides direct access to highly functionalised cyclohexane derivatives.

Carbocyclic ring closure of unsaturated S-, Se-, and C-aryl glycosides

Sollogoub, Matthieu,Mallet, Jean-Maurice,Sinay, Pierre

, p. 362 - 364 (2007/10/03)

Triisobutylaluminum-promoted rearrangement of unsaturated glycosides containing electron-donating aglycons - such as C-aryl glycoside 1, or O-, S- , and Seglycosides - provides direct access to highly functionalized cyclohexane derivatives such as 2.

The First Direct Method for C-Glucopyranosyl Derivatization of 2,3,4,6-Tetra-O-benzyl-D-glucopyranose

Allevi, Pietro,Anastasia, Mario,Ciuffreda, Pierangela,Fiecchi, Alberto,Scala, Antonio

, p. 1245 - 1246 (2007/10/02)

Commercially available 2,3,4,6-tetra-O-benzyl-D-glucopyranose, activated by trifluoroacetic anhydride reacts, in the presence of Lewis acids, with various silyl enol ethers or with allylsilane to yield C-D-glucopyranosyl derivatives of the α-configuration

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