Cas 245369-13-5,3-((2S,3S,4S,5R,6R)-2-Allyl-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-3-yloxy)-pent-4-ene-1,2-diol

245369-13-5

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Basic information

Product Name: 3-((2S,3S,4S,5R,6R)-2-Allyl-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-3-yloxy)-pent-4-ene-1,2-diol
Synonyms: 3-((2S,3S,4S,5R,6R)-2-Allyl-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-3-yloxy)-pent-4-ene-1,2-diol
CAS NO:245369-13-5
Molecular Formula:
Molecular Weight: 574.714
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-((2S,3S,4S,5R,6R)-2-Allyl-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-3-yloxy)-pent-4-ene-1,2-diol(CAS DataBase Reference)
NIST Chemistry Reference: 3-((2S,3S,4S,5R,6R)-2-Allyl-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-3-yloxy)-pent-4-ene-1,2-diol(245369-13-5)
EPA Substance Registry System: 3-((2S,3S,4S,5R,6R)-2-Allyl-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-3-yloxy)-pent-4-ene-1,2-diol(245369-13-5)

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: 245369-13-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 245369-13-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,3,6 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 245369-13:
(8*2)+(7*4)+(6*5)+(5*3)+(4*6)+(3*9)+(2*1)+(1*3)=145
145 % 10 = 5
So 245369-13-5 is a valid CAS Registry Number.

245369-13-5Upstream product

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245369-13-5Relevant academic research and scientific papers

Expeditious tandem-metathesis route to the AB-ring fragment of ciguatoxin

Oguri, Hiroki,Sasaki, Shin-ya,Oishi, Tohru,Hirama, Masahiro

, p. 5405 - 5408 (1999)

The AB-ring fragment of ciguatoxin was synthesized in ten steps from tri-O-benzyl-D-glucal based on a highly diastereoselective ring-closing metathesis and subsequent cross metathesis.

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