Cas 246137-20-2,(3aR,4S,6aR)-6-(Benzyloxymethyl)-4-(triisopropylsilyloxy)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol

246137-20-2

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Basic information

Product Name: (3aR,4S,6aR)-6-(Benzyloxymethyl)-4-(triisopropylsilyloxy)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol
Synonyms: (3aR,4S,6aR)-6-(Benzyloxymethyl)-4-(triisopropylsilyloxy)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol
CAS NO:246137-20-2
Molecular Formula:
Molecular Weight: 432.676
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: (3aR,4S,6aR)-6-(Benzyloxymethyl)-4-(triisopropylsilyloxy)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,4S,6aR)-6-(Benzyloxymethyl)-4-(triisopropylsilyloxy)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol(246137-20-2)
EPA Substance Registry System: (3aR,4S,6aR)-6-(Benzyloxymethyl)-4-(triisopropylsilyloxy)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol(246137-20-2)

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: 246137-20-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 246137-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,6,1,3 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 246137-20:
(8*2)+(7*4)+(6*6)+(5*1)+(4*3)+(3*7)+(2*2)+(1*0)=122
122 % 10 = 2
So 246137-20-2 is a valid CAS Registry Number.

246137-20-2Upstream product

246137-20-2Downstream Products

243462-53-5 (4aS)-4,4a-Anhydro-5-O-benzyl-4a-carba-1-O-(triisopropylsilyl)-2,3-O-isopropylidene-β-L-lyxofuranose

246137-20-2Relevant academic research and scientific papers

Chiral pool synthesis of 4a-substituted carbocyclic cyclopentanoid nucleoside precursors, I

Csuk, Rene,Doerr, Petra,Kuehn, Martin,Krieger, Claus,Antipin, Mikhael Y.

, p. 1068 - 1078 (2007/10/03)

A suitable protected D-ribono-1,4-lactone derivative has been used for the straightforward chiral pool synthesis of cyclopentanoid nucleoside precursors. Thus, epoxidation followed by deoxygenation or regioselective ring opening led to nucleoside precurso

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