Cas 153186-19-7,3,5-O-(p-methoxybenzylidene)-4-C-hydroxymethyl-1,2-O-isopropylidene-α-D-xylofuranose

153186-19-7

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Basic information

Product Name: 3,5-O-(p-methoxybenzylidene)-4-C-hydroxymethyl-1,2-O-isopropylidene-α-D-xylofuranose
Synonyms: 3,5-O-(p-methoxybenzylidene)-4-C-hydroxymethyl-1,2-O-isopropylidene-α-D-xylofuranose
CAS NO:153186-19-7
Molecular Formula:
Molecular Weight: 338.357
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: 3,5-O-(p-methoxybenzylidene)-4-C-hydroxymethyl-1,2-O-isopropylidene-α-D-xylofuranose(CAS DataBase Reference)
NIST Chemistry Reference: 3,5-O-(p-methoxybenzylidene)-4-C-hydroxymethyl-1,2-O-isopropylidene-α-D-xylofuranose(153186-19-7)
EPA Substance Registry System: 3,5-O-(p-methoxybenzylidene)-4-C-hydroxymethyl-1,2-O-isopropylidene-α-D-xylofuranose(153186-19-7)

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: 153186-19-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 153186-19-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,1,8 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 153186-19:
(8*1)+(7*5)+(6*3)+(5*1)+(4*8)+(3*6)+(2*1)+(1*9)=127
127 % 10 = 7
So 153186-19-7 is a valid CAS Registry Number.

153186-19-7Upstream product

153186-18-6 1,2-O-isopropylidene-4-C-hydroxymethyl-3-O-(p-methoxybenzyl)-β-L-threo-pentofuranose

153186-19-7Downstream Products

153186-20-0 3,5-O-(p-methoxybenzylidene)-4-C-iodomethyl-1,2-O-isopropylidene-α-D-xylofuranose

153186-19-7Relevant academic research and scientific papers

Synthesis of 4'-C-methylnucleosides.

Waga,Nishizaki,Miyakawa,Ohrui,Meguro

, p. 1433 - 1438 (1993)

Several 4'-C-methylnucleosides were prepared. 1H-NMR studies on these nucleotides showed that they have the 3'-exo furanose ring conformation different from the 3'-endo conformation of natural nucleosides.

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