Cas 404391-02-2,4,5,6,7-Tetrachloro-2-((2R,4aR,6S,7R,8R,8aS)-8-hydroxy-2-phenyl-6-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-isoindole-1,3-dione

404391-02-2

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Basic information

Product Name: 4,5,6,7-Tetrachloro-2-((2R,4aR,6S,7R,8R,8aS)-8-hydroxy-2-phenyl-6-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-isoindole-1,3-dione
Synonyms: 4,5,6,7-Tetrachloro-2-((2R,4aR,6S,7R,8R,8aS)-8-hydroxy-2-phenyl-6-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-isoindole-1,3-dione
CAS NO:404391-02-2
Molecular Formula:
Molecular Weight: 627.329
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4,5,6,7-Tetrachloro-2-((2R,4aR,6S,7R,8R,8aS)-8-hydroxy-2-phenyl-6-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-isoindole-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 4,5,6,7-Tetrachloro-2-((2R,4aR,6S,7R,8R,8aS)-8-hydroxy-2-phenyl-6-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-isoindole-1,3-dione(404391-02-2)
EPA Substance Registry System: 4,5,6,7-Tetrachloro-2-((2R,4aR,6S,7R,8R,8aS)-8-hydroxy-2-phenyl-6-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-isoindole-1,3-dione(404391-02-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 404391-02-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 404391-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,4,3,9 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 404391-02:
(8*4)+(7*0)+(6*4)+(5*3)+(4*9)+(3*1)+(2*0)+(1*2)=112
112 % 10 = 2
So 404391-02-2 is a valid CAS Registry Number.

404391-02-2Upstream product

217814-68-1 1-phenylsulfenyl-3,4,6-tri-O-acetyl-1,2-dideoxy-2-N-tetrachlorophthalimido-β-D-glucopyranoside

404391-02-2Downstream Products

404391-02-2Relevant academic research and scientific papers

Dialkylphosphates as stereodirecting protecting groups in oligosaccharide synthesis

Yamada, Takeshi,Takemura, Kazunobu,Yoshida, Jun-Ichi,Yamago, Shigeru

, p. 7575 - 7578 (2008/02/01)

(Chemical Equation Presented) Double duty: A phosphoric ester at the C2 position in glycosyl donors directs the glycosylation to occur selectively at the anomeric carbon atom with complete 1,2-trans selectivity. Since the phosphoric ester can be removed to give the hydroxy function, this group serves as a stereodirecting protecting group in oligosaccharide synthesis.

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