Cas 130412-91-8,(6R,7R,10R)-7-Isopropyl-5-(4-methoxy-phenyl)-10-methyl-1-oxa-5-aza-spiro[5.5]undecane-2,4-dione

130412-91-8

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Basic information

Product Name: (6R,7R,10R)-7-Isopropyl-5-(4-methoxy-phenyl)-10-methyl-1-oxa-5-aza-spiro[5.5]undecane-2,4-dione
Synonyms:
CAS NO:130412-91-8
Molecular Formula:
Molecular Weight: 345.439
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,10R)-7-Isopropyl-5-(4-methoxy-phenyl)-10-methyl-1-oxa-5-aza-spiro[5.5]undecane-2,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: (6R,7R,10R)-7-Isopropyl-5-(4-methoxy-phenyl)-10-methyl-1-oxa-5-aza-spiro[5.5]undecane-2,4-dione(130412-91-8)
EPA Substance Registry System: (6R,7R,10R)-7-Isopropyl-5-(4-methoxy-phenyl)-10-methyl-1-oxa-5-aza-spiro[5.5]undecane-2,4-dione(130412-91-8)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 130412-91-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 130412-91-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,4,1 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 130412-91:
(8*1)+(7*3)+(6*0)+(5*4)+(4*1)+(3*2)+(2*9)+(1*1)=78
78 % 10 = 8
So 130412-91-8 is a valid CAS Registry Number.

130412-91-8Upstream product

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130412-91-8Relevant academic research and scientific papers

CHIRAL SPIROCYCLIC 1,3-OXAZINE-4,6-DIONES AS NOVEL SYNTHONS FOR ENANTIOMERICALLY PURE COMPOUNDS

Sato, Masayuki,Hisamichi, Hiroyuki,Kitazawa, Noritaka,Kaneko, Chikara,Furuya, Toshio,et al.

, p. 3605 - 3608 (2007/10/02)

Chiral spirocyclic 1,3-oxazine-4,6-diones have been synthesized from 1-menthone.Base-catalysed alkylation of the 5-monosubstituted derivatives provides an efficient synthetic method of enantiomerically pure malonamic acids.

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