Cas 115129-99-2,(R)-1,4-anhydro-5-O-<(1,1-dimethylethyl)dimethylsilyl>-2,3-O-(1-methylethylidene)-1-C-(4-methylphenyl)-D-ribitol

115129-99-2

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Basic information

Product Name: (R)-1,4-anhydro-5-O-<(1,1-dimethylethyl)dimethylsilyl>-2,3-O-(1-methylethylidene)-1-C-(4-methylphenyl)-D-ribitol
Synonyms:
CAS NO:115129-99-2
Molecular Formula:
Molecular Weight: 378.584
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: (R)-1,4-anhydro-5-O-<(1,1-dimethylethyl)dimethylsilyl>-2,3-O-(1-methylethylidene)-1-C-(4-methylphenyl)-D-ribitol(CAS DataBase Reference)
NIST Chemistry Reference: (R)-1,4-anhydro-5-O-<(1,1-dimethylethyl)dimethylsilyl>-2,3-O-(1-methylethylidene)-1-C-(4-methylphenyl)-D-ribitol(115129-99-2)
EPA Substance Registry System: (R)-1,4-anhydro-5-O-<(1,1-dimethylethyl)dimethylsilyl>-2,3-O-(1-methylethylidene)-1-C-(4-methylphenyl)-D-ribitol(115129-99-2)

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: 115129-99-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 115129-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,1,2 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 115129-99:
(8*1)+(7*1)+(6*5)+(5*1)+(4*2)+(3*9)+(2*9)+(1*9)=112
112 % 10 = 2
So 115129-99-2 is a valid CAS Registry Number.

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115129-99-2Relevant academic research and scientific papers

NEW APPROACHES TO SYNTHETIC RECEPTORS. STUDIES ON THE SYNTHESIS AND PROPERTIES OF MACROCYCLIC C-GLYCOSYL COMPOUNDS AS CHIRAL, WATER-SOLUBLE CYCLOPHANES

Wilcox, Craig S.,Cowart, Marlon D.

, p. 141 - 160 (2007/10/02)

In an approach for the preparation of macrocyclic C-glycosyl compounds, the C-glycosyl residue is synthesized by acid assisted reduction of a cyclic hemiacetal with sodium cyanoborohydride.Macrocyclic formation is effected by the reaction of a symmetrical

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