Cas 226950-22-7,((4R,5R)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-tert-butyl-dimethyl-silane

226950-22-7

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Basic information

Product Name: ((4R,5R)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-tert-butyl-dimethyl-silane
Synonyms: ((4R,5R)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-tert-butyl-dimethyl-silane
CAS NO:226950-22-7
Molecular Formula:
Molecular Weight: 366.573
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: ((4R,5R)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-tert-butyl-dimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: ((4R,5R)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-tert-butyl-dimethyl-silane(226950-22-7)
EPA Substance Registry System: ((4R,5R)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-tert-butyl-dimethyl-silane(226950-22-7)

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: 226950-22-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 226950-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,9,5 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 226950-22:
(8*2)+(7*2)+(6*6)+(5*9)+(4*5)+(3*0)+(2*2)+(1*2)=137
137 % 10 = 7
So 226950-22-7 is a valid CAS Registry Number.

226950-22-7Upstream product

151359-19-2 (E)-1-(Benzyloxy)-4-<(tert-butyldimethylsilyl)oxy>-2-butene

226950-22-7Downstream Products

78469-77-9 1-O-benzyl-2,3-O-isopropylidene-D-threitol

226950-22-7Relevant academic research and scientific papers

Synthesis of Carbohydrates and Related Polyhydroxylated Compounds Employing Asymmetric Dihydroxylation. 1. An Access to Erythro-diols

Ko, Soo Y.,Malik, Majbeen

, p. 4675 - 4678 (1993)

Asymmetric dihydroxylation provides an easy access to tetrose: threose directly from the (E)-olefin 1, and erythrose via an irreversible Payne-type rearrangement - opening process of the threitol cyclic sulfate 5.

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