Cas 1244032-48-1,(2R)-2-[2-(1-benzyloxyethyl)-1,3-dioxolan-2-yl]-4,5-dimethoxynapghthalen-1-ol

1244032-48-1

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Basic information

Product Name: (2R)-2-[2-(1-benzyloxyethyl)-1,3-dioxolan-2-yl]-4,5-dimethoxynapghthalen-1-ol
Synonyms: (2R)-2-[2-(1-benzyloxyethyl)-1,3-dioxolan-2-yl]-4,5-dimethoxynapghthalen-1-ol
CAS NO:1244032-48-1
Molecular Formula:
Molecular Weight: 410.467
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)-2-[2-(1-benzyloxyethyl)-1,3-dioxolan-2-yl]-4,5-dimethoxynapghthalen-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (2R)-2-[2-(1-benzyloxyethyl)-1,3-dioxolan-2-yl]-4,5-dimethoxynapghthalen-1-ol(1244032-48-1)
EPA Substance Registry System: (2R)-2-[2-(1-benzyloxyethyl)-1,3-dioxolan-2-yl]-4,5-dimethoxynapghthalen-1-ol(1244032-48-1)

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: 1244032-48-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1244032-48-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,4,0,3 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1244032-48:
(9*1)+(8*2)+(7*4)+(6*4)+(5*0)+(4*3)+(3*2)+(2*4)+(1*8)=111
111 % 10 = 1
So 1244032-48-1 is a valid CAS Registry Number.

1244032-48-1Upstream product

1244032-44-7 (2R)-2-(1-benzyloxyethyl)-2-ethynyl-1,3-dioxolane

1244032-48-1Downstream Products

1244032-49-2 (2R)-2-(1-benzyloxyethyl)-2-(1,4,5-trimethoxynaphthalen-2-yl)-1,3-dioxolane

1244032-48-1Relevant academic research and scientific papers

A concise asymmetric synthesis of (-)-hongconin and (-)-1-epi-hongconin

Fernandes, Rodney A.,Chavan, Vijay P.

, p. 4306 - 4311 (2010)

A concise asymmetric synthesis of (-)-hongconin and (-)-1epi-hongconin is described. The synthesis features an efficient combination of Doetz benzannulation or lactaldehyde arylation and the oxa-Pictet-Spengler reaction as the key steps. The synthesis is

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