Cas 1335018-87-5,(3R,4'S)-1-benzyl-4'-(4,4-dimethyl-2-oxooxazolidine-3-carbonyl)-2'-thioxospiro[indoline-3,5'-oxazolidin]-2-one

1335018-87-5

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Basic information

Product Name: (3R,4'S)-1-benzyl-4'-(4,4-dimethyl-2-oxooxazolidine-3-carbonyl)-2'-thioxospiro[indoline-3,5'-oxazolidin]-2-one
Synonyms: (3R,4'S)-1-benzyl-4'-(4,4-dimethyl-2-oxooxazolidine-3-carbonyl)-2'-thioxospiro[indoline-3,5'-oxazolidin]-2-one
CAS NO:1335018-87-5
Molecular Formula:
Molecular Weight: 451.503
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: (3R,4'S)-1-benzyl-4'-(4,4-dimethyl-2-oxooxazolidine-3-carbonyl)-2'-thioxospiro[indoline-3,5'-oxazolidin]-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4'S)-1-benzyl-4'-(4,4-dimethyl-2-oxooxazolidine-3-carbonyl)-2'-thioxospiro[indoline-3,5'-oxazolidin]-2-one(1335018-87-5)
EPA Substance Registry System: (3R,4'S)-1-benzyl-4'-(4,4-dimethyl-2-oxooxazolidine-3-carbonyl)-2'-thioxospiro[indoline-3,5'-oxazolidin]-2-one(1335018-87-5)

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: 1335018-87-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1335018-87-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,5,0,1 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1335018-87:
(9*1)+(8*3)+(7*3)+(6*5)+(5*0)+(4*1)+(3*8)+(2*8)+(1*7)=135
135 % 10 = 5
So 1335018-87-5 is a valid CAS Registry Number.

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1335018-87-5Relevant academic research and scientific papers

Organocatalytic enantioselective tandem aldol-cyclization reaction of α-isothiocyanato imides and activated carbonyl compounds

Guang, Jie,Zhao, Cong-Gui

, p. 1205 - 1211 (2011)

The organocatalytic enantioselective tandem aldol-cyclization reactions of α-isothiocyanato imides and activated carbonyl compounds, such as isatins, an α-ketolactone and a 1,2-dione, have been studied with cinchona alkaloid-derived thiourea-catalysts. Th

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