Cas 484000-92-2,[(3aS,4S,6R,7R,7aS)-7-(2-Bromo-4,5-dimethoxy-benzyloxy)-4-methoxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ylmethoxy]-tert-butyl-dimethyl-silane

484000-92-2

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Basic information

Product Name: [(3aS,4S,6R,7R,7aS)-7-(2-Bromo-4,5-dimethoxy-benzyloxy)-4-methoxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ylmethoxy]-tert-butyl-dimethyl-silane
Synonyms:
CAS NO:484000-92-2
Molecular Formula:
Molecular Weight: 577.585
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: [(3aS,4S,6R,7R,7aS)-7-(2-Bromo-4,5-dimethoxy-benzyloxy)-4-methoxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ylmethoxy]-tert-butyl-dimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: [(3aS,4S,6R,7R,7aS)-7-(2-Bromo-4,5-dimethoxy-benzyloxy)-4-methoxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ylmethoxy]-tert-butyl-dimethyl-silane(484000-92-2)
EPA Substance Registry System: [(3aS,4S,6R,7R,7aS)-7-(2-Bromo-4,5-dimethoxy-benzyloxy)-4-methoxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ylmethoxy]-tert-butyl-dimethyl-silane(484000-92-2)

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: 484000-92-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 484000-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,4,0,0 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 484000-92:
(8*4)+(7*8)+(6*4)+(5*0)+(4*0)+(3*0)+(2*9)+(1*2)=132
132 % 10 = 2
So 484000-92-2 is a valid CAS Registry Number.

484000-92-2Upstream product

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484000-92-2Relevant academic research and scientific papers

Synthesis of chiral trans-fused pyrano[3,2-c][2]benzoxocines from D-mannose by regioselective 8-endo-aryl radical cyclization

Nandi, Aniruddha,Chattopadhyay, Partha

, p. 5977 - 5980 (2007/10/03)

A simple chiral synthesis of trans-pyrano[3,2-c][2]benzoxocines 8a-d in good yields (60-75%) through regioselective 8-endo-trig aryl radical cyclization of the D-mannose derived enopyranosides 7a-d with Bu3SnH is described.

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