Cas 260444-81-3,[3-((3aR,4R,6S,6aR)-2,2-Dimethyl-6-phenylselanyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethoxy)-prop-1-ynyl]-trimethyl-silane

260444-81-3

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Basic information

Product Name: [3-((3aR,4R,6S,6aR)-2,2-Dimethyl-6-phenylselanyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethoxy)-prop-1-ynyl]-trimethyl-silane
Synonyms:
CAS NO:260444-81-3
Molecular Formula:
Molecular Weight: 439.485
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-((3aR,4R,6S,6aR)-2,2-Dimethyl-6-phenylselanyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethoxy)-prop-1-ynyl]-trimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: [3-((3aR,4R,6S,6aR)-2,2-Dimethyl-6-phenylselanyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethoxy)-prop-1-ynyl]-trimethyl-silane(260444-81-3)
EPA Substance Registry System: [3-((3aR,4R,6S,6aR)-2,2-Dimethyl-6-phenylselanyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethoxy)-prop-1-ynyl]-trimethyl-silane(260444-81-3)

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: 260444-81-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 260444-81-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,0,4,4 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 260444-81:
(8*2)+(7*6)+(6*0)+(5*4)+(4*4)+(3*4)+(2*8)+(1*1)=123
123 % 10 = 3
So 260444-81-3 is a valid CAS Registry Number.

260444-81-3Upstream product

260444-81-3Downstream Products

260444-81-3Relevant academic research and scientific papers

C-glycosylation via radical cyclization: Synthetic application to a new C-glycoside

Kim, Guncheol,Kim, Hee Seok

, p. 225 - 227 (2000)

Radical cyclization of ribo-phenylselenoglycoside tethered with propargyl moieties on C-5 hydroxyl group afforded new potential intermediates for the synthesis of C-nucleoside derivatives.

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