Cas 135360-89-3,tert-butyl (4'R,7R,8R)-9-oxo-8-(2'-oxo-4'-phenyl-1',3'-oxazolidin-3'-yl)-1,2-diazabicyclo<5.2.0>nona-3,5-diene-2-carboxylate

135360-89-3

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Basic information

Product Name: tert-butyl (4'R,7R,8R)-9-oxo-8-(2'-oxo-4'-phenyl-1',3'-oxazolidin-3'-yl)-1,2-diazabicyclo<5.2.0>nona-3,5-diene-2-carboxylate
Synonyms:
CAS NO:135360-89-3
Molecular Formula:
Molecular Weight: 397.431
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: tert-butyl (4'R,7R,8R)-9-oxo-8-(2'-oxo-4'-phenyl-1',3'-oxazolidin-3'-yl)-1,2-diazabicyclo<5.2.0>nona-3,5-diene-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (4'R,7R,8R)-9-oxo-8-(2'-oxo-4'-phenyl-1',3'-oxazolidin-3'-yl)-1,2-diazabicyclo<5.2.0>nona-3,5-diene-2-carboxylate(135360-89-3)
EPA Substance Registry System: tert-butyl (4'R,7R,8R)-9-oxo-8-(2'-oxo-4'-phenyl-1',3'-oxazolidin-3'-yl)-1,2-diazabicyclo<5.2.0>nona-3,5-diene-2-carboxylate(135360-89-3)

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: 135360-89-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135360-89-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,3,6 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135360-89:
(8*1)+(7*3)+(6*5)+(5*3)+(4*6)+(3*0)+(2*8)+(1*9)=123
123 % 10 = 3
So 135360-89-3 is a valid CAS Registry Number.

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135360-89-3Relevant academic research and scientific papers

Asymmetric Synthesis of Diazepino-β-lactams by Cycloaddition of an 'Evans-Sjogren' Ketene with 1H-1,2-Diazepines

Muller, Marc,Bur, Daniel,Tschamber, Theophile,Streith, Jacques

, p. 767 - 773 (2007/10/02)

The ketene derivative of the chiral oxazolidone 1 underwent non-converted stereospecific cycloadditions with the (Z)-imine moiety of diazepines 2, leading thereby with good diastereoselection to the trans-β-lactam adducts 3 (major) and 4 (minor).T

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