Cas 1374982-11-2,(2S,6R)-benzyl 2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-6-methoxymorpholine-4-carboxylate

1374982-11-2

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Basic information

Product Name: (2S,6R)-benzyl 2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-6-methoxymorpholine-4-carboxylate
Synonyms:
CAS NO:1374982-11-2
Molecular Formula:
Molecular Weight: 410.426
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: (2S,6R)-benzyl 2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-6-methoxymorpholine-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,6R)-benzyl 2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-6-methoxymorpholine-4-carboxylate(1374982-11-2)
EPA Substance Registry System: (2S,6R)-benzyl 2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-6-methoxymorpholine-4-carboxylate(1374982-11-2)

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: 1374982-11-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1374982-11-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,9,8 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1374982-11:
(9*1)+(8*3)+(7*7)+(6*4)+(5*9)+(4*8)+(3*2)+(2*1)+(1*1)=192
192 % 10 = 2
So 1374982-11-2 is a valid CAS Registry Number.

1374982-11-2Upstream product

501-53-1 benzyl chloroformate

1374982-11-2Downstream Products

1374982-11-2Relevant academic research and scientific papers

Stereocontrolled access to optically-enriched oxabispidines

Brice, Heloise,Gill, Duncan M.,Goldie, Laura,Keegan, Philip S.,Kerr, William J.,Svensson, Per H.

supporting information; experimental part, p. 4836 - 4838 (2012/06/16)

A range of chiral, optically-enriched bicyclic oxabispidines were prepared from (S)-(-)-2,3-epoxypropylphthalimide using an efficient sequence featuring a stereocontrolled intramolecular Mannich reaction as the key transformation.

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