Cas 1279018-06-2,(S)-tert-butyl 2-((S)-3,4-dichloro-5-oxo-2,5-dihydrofuran-2-yl)-2-hydroxy-2-(4-methoxyphenyl)acetate

1279018-06-2

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Basic information

Product Name: (S)-tert-butyl 2-((S)-3,4-dichloro-5-oxo-2,5-dihydrofuran-2-yl)-2-hydroxy-2-(4-methoxyphenyl)acetate
Synonyms:
CAS NO:1279018-06-2
Molecular Formula:
Molecular Weight: 389.232
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: (S)-tert-butyl 2-((S)-3,4-dichloro-5-oxo-2,5-dihydrofuran-2-yl)-2-hydroxy-2-(4-methoxyphenyl)acetate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-tert-butyl 2-((S)-3,4-dichloro-5-oxo-2,5-dihydrofuran-2-yl)-2-hydroxy-2-(4-methoxyphenyl)acetate(1279018-06-2)
EPA Substance Registry System: (S)-tert-butyl 2-((S)-3,4-dichloro-5-oxo-2,5-dihydrofuran-2-yl)-2-hydroxy-2-(4-methoxyphenyl)acetate(1279018-06-2)

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: 1279018-06-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1279018-06-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,9,0,1 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1279018-06:
(9*1)+(8*2)+(7*7)+(6*9)+(5*0)+(4*1)+(3*8)+(2*0)+(1*6)=162
162 % 10 = 2
So 1279018-06-2 is a valid CAS Registry Number.

1279018-06-2Upstream product

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1279018-06-2Relevant academic research and scientific papers

The direct asymmetric vinylogous aldol reaction of furanones with α-ketoesters: Access to chiral γ-Butenolides and glycerol derivatives

Luo, Jie,Wang, Haifei,Han, Xiao,Xu, Li-Wen,Kwiatkowski, Jacek,Huang, Kuo-Wei,Lu, Yixin

supporting information; experimental part, p. 1861 - 1864 (2011/04/22)

Twice as good: The title reaction using the tryptophan-derived bifunctional organic catalyst 1 has been developed. The reported method led to the synthesis of chiral γ-substituted butenolides in excellent yields, with high diastereo- and enantioselectivit

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