Cas 232603-19-9,(2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-[3-((1R,2S,3R)-2,3-bis-benzyloxy-1-benzyloxymethyl-pent-4-enyloxy)-but-3-enyl]-tetrahydro-pyran

232603-19-9

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Basic information

Product Name: (2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-[3-((1R,2S,3R)-2,3-bis-benzyloxy-1-benzyloxymethyl-pent-4-enyloxy)-but-3-enyl]-tetrahydro-pyran
Synonyms: (2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-[3-((1R,2S,3R)-2,3-bis-benzyloxy-1-benzyloxymethyl-pent-4-enyloxy)-but-3-enyl]-tetrahydro-pyran
CAS NO:232603-19-9
Molecular Formula:
Molecular Weight: 995.265
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: (2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-[3-((1R,2S,3R)-2,3-bis-benzyloxy-1-benzyloxymethyl-pent-4-enyloxy)-but-3-enyl]-tetrahydro-pyran(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-[3-((1R,2S,3R)-2,3-bis-benzyloxy-1-benzyloxymethyl-pent-4-enyloxy)-but-3-enyl]-tetrahydro-pyran(232603-19-9)
EPA Substance Registry System: (2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-[3-((1R,2S,3R)-2,3-bis-benzyloxy-1-benzyloxymethyl-pent-4-enyloxy)-but-3-enyl]-tetrahydro-pyran(232603-19-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 232603-19-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 232603-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,2,6,0 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 232603-19:
(8*2)+(7*3)+(6*2)+(5*6)+(4*0)+(3*3)+(2*1)+(1*9)=99
99 % 10 = 9
So 232603-19-9 is a valid CAS Registry Number.

232603-19-9Upstream product

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232603-19-9Relevant academic research and scientific papers

Convergent preparation of 1,6-linked C-disaccharides via olefin metathesis

Postema, Maarten H. D.,Calimente, Daniel

, p. 4755 - 4759 (2007/10/03)

The DCC mediated coupling reaction of 3,4,6-tri-O-benzyl-1,2-dideoxy-D- arabino-hex-1-enitol (5a) with a variety of sugar based carboxylic acids 6a- d gave esters 7a-d in good yield. Methylenation of the formed esters led to the acyclic enol ethers 8a-d a

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