Cas 1242065-90-2,(1R)-1-methyl-2-[(2S,3R)-3-vinyloxiran-2-yl]ethyl (3R)-3-[(4-methoxybenzyl)oxy]-4-pentenoate

1242065-90-2

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Basic information

Product Name: (1R)-1-methyl-2-[(2S,3R)-3-vinyloxiran-2-yl]ethyl (3R)-3-[(4-methoxybenzyl)oxy]-4-pentenoate
Synonyms: (1R)-1-methyl-2-[(2S,3R)-3-vinyloxiran-2-yl]ethyl (3R)-3-[(4-methoxybenzyl)oxy]-4-pentenoate
CAS NO:1242065-90-2
Molecular Formula:
Molecular Weight: 346.423
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: (1R)-1-methyl-2-[(2S,3R)-3-vinyloxiran-2-yl]ethyl (3R)-3-[(4-methoxybenzyl)oxy]-4-pentenoate(CAS DataBase Reference)
NIST Chemistry Reference: (1R)-1-methyl-2-[(2S,3R)-3-vinyloxiran-2-yl]ethyl (3R)-3-[(4-methoxybenzyl)oxy]-4-pentenoate(1242065-90-2)
EPA Substance Registry System: (1R)-1-methyl-2-[(2S,3R)-3-vinyloxiran-2-yl]ethyl (3R)-3-[(4-methoxybenzyl)oxy]-4-pentenoate(1242065-90-2)

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: 1242065-90-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1242065-90-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,2,0,6 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1242065-90:
(9*1)+(8*2)+(7*4)+(6*2)+(5*0)+(4*6)+(3*5)+(2*9)+(1*0)=122
122 % 10 = 2
So 1242065-90-2 is a valid CAS Registry Number.

1242065-90-2Upstream product

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1242065-90-2Relevant academic research and scientific papers

Total synthesis of decarestrictine i and botryolide B via RCM protocol

Radha Krishna, Palakodety,Rao, T. Jagannadha

supporting information; experimental part, p. 3130 - 3132 (2010/08/21)

A convergent stereoselective total synthesis of decarestrictine I (1) and botryolide B (1a) invoking a common synthetic strategy is reported. The key steps are: ring-closing metathesis of epoxy dienoic esters obtained through the Yamaguchi esterification

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