Cas 1354716-16-7,(6R,7R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-6-hydroxy-7-methyl-3-methylene-8-oxooct-4-en-2-yl benzoate

1354716-16-7

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Basic information

Product Name: (6R,7R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-6-hydroxy-7-methyl-3-methylene-8-oxooct-4-en-2-yl benzoate
Synonyms: (6R,7R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-6-hydroxy-7-methyl-3-methylene-8-oxooct-4-en-2-yl benzoate
CAS NO:1354716-16-7
Molecular Formula:
Molecular Weight: 463.53
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: (6R,7R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-6-hydroxy-7-methyl-3-methylene-8-oxooct-4-en-2-yl benzoate(CAS DataBase Reference)
NIST Chemistry Reference: (6R,7R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-6-hydroxy-7-methyl-3-methylene-8-oxooct-4-en-2-yl benzoate(1354716-16-7)
EPA Substance Registry System: (6R,7R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-6-hydroxy-7-methyl-3-methylene-8-oxooct-4-en-2-yl benzoate(1354716-16-7)

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: 1354716-16-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1354716-16-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,4,7,1 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1354716-16:
(9*1)+(8*3)+(7*5)+(6*4)+(5*7)+(4*1)+(3*6)+(2*1)+(1*6)=157
157 % 10 = 7
So 1354716-16-7 is a valid CAS Registry Number.

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1354716-16-7Relevant academic research and scientific papers

Alkene metathesis approach to β-unsubstituted anti -allylic alcohols and their use in ene-yne metathesis

Clark, Joseph R.,French, Jonathan M.,Diver, Steven T.

, p. 1599 - 1604 (2012/04/04)

The synthesis of β-unsubstituted, anti-allylic alcohols using a catalytic Evans aldol reaction conjoined with a relay-type ring-closing alkene metathesis is reported. The metathesis step serves to remove a β-alkenyl group, which facilitated the aldol step

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