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3,4,5,7-tetra-O-benzyl-1,2,6-trideoxy-D-galacto-hept-1-en-6-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

176540-14-0

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176540-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176540-14-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,5,4 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 176540-14:
(8*1)+(7*7)+(6*6)+(5*5)+(4*4)+(3*0)+(2*1)+(1*4)=140
140 % 10 = 0
So 176540-14-0 is a valid CAS Registry Number.

176540-14-0Relevant academic research and scientific papers

Divergent synthesis of aminocyclopentitol analogues via stereoselective amination of cyclic polybenzyl ether with chlorosulfonyl isocyanate

Jung, Young Hoon,Kim, Seung In,Hong, Yeon Ju,Park, Sook Jin,Kang, Kyung Tae,Kim, So Yeon,Park, Jung Sang,Kim, In Su

, p. 1089 - 1092 (2015)

Abstract The divergent synthesis of some novel aminocyclopentitol analogues was concisely achieved from readily available d-galactose via the highly diastereoselective amination of carbocyclic polybenzyl ether using chlorosulfonyl isocyanate, diastereosel

Enantioselective synthesis of carba-L-furanose precursors of carbanucleosides, using ring-closing metathesis

Gillaizeau, Isabelle,Charamon, Steve,Agrofoglio, Luigi A

, p. 8817 - 8819 (2001)

Carba-L-sugars were synthesized in seven steps from known tetra-O-benzyl-D-galactopyranose (3). The synthesis of cyclopentene ring has been accomplished via a ring-closing metathesis step. Schrock's catalyst was employed on the unique diene, key intermedi

Total synthesis of carbocyclic nucleoside (+)-neplanocin A

Jung, Young Hoon,Kim, Seung In,Hong, Yeon Ju,Park, Sook Jin,Kang, Kyung Tae,Kim, So Yeon,Kim, In Su

, p. 1068 - 1073 (2015/01/30)

Asymmetric total synthesis of (+)-neplanocin A was concisely achieved from readily available d-galactose via the regioselective and diastereoselective amination of carbocyclic polybenzyl ether using chlorosulfonyl isocyanate and intramolecular olefin meta

Intramolecular ketonitrone-olefin cycloaddition reaction: direct and stereocontrolled synthesis of nitrogenated quaternary centered aminocyclopentitols as galactosidase inhibitors

Suman Reddy,Kadigachalam,Doddi, Venkata Ramana,Vankar, Yashwant D.

scheme or table, p. 5827 - 5830 (2010/01/11)

Synthesis of nitrogenated quaternary centered polyhydroxylated aminocyclopentanes by implementation of ketonitrone-olefin cycloaddition reaction as a key step has been accomplished in a stereocontrolled manner. The target molecules were found to be modera

Synthetic iminosugar derivatives as new potential immunosuppressive agents

Ye, Xin-Shan,Sun, Fang,Liu, Min,Li, Qin,Wang, Yuhang,Zhang, Guisheng,Zhang, Li-He,Zhang, Xiao-Lian

, p. 3688 - 3691 (2007/10/03)

Several iminosugar derivatives were synthesized, and their effects on the secretion of IL-4 and IFN-γ from the mouse splenocytes were examined. The effects on membrane expression of other T cell-associated molecules (CD3, CD4, CD8) and B cell-associated m

An efficient synthetic approach to aza-C-glycosyl compounds. Application to the synthesis of an aza-C-disaccharide

Martin, Olivier R.,Liu, Li,Yang, Feng

, p. 1991 - 1994 (2007/10/03)

The NIS-mediated cyclization of aminoheptenitols 5-8 (prepared in three steps from tetra-O-benzyl-D-hexopyranoses) provided 1,2,6-trideoxy-2,6-imino-l-iodoheptitol derivatives 9-12, respectively, highly stereoselectively and in high yield. The "α-D-glucoα

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