Cas 1246868-07-4,(R)-1-((4S,5S)-2,2-dimethyl-5-((E)-styryl)-1,3-dioxolan-4-yl)ethyl acetate

1246868-07-4

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Basic information

Product Name: (R)-1-((4S,5S)-2,2-dimethyl-5-((E)-styryl)-1,3-dioxolan-4-yl)ethyl acetate
Synonyms: (R)-1-((4S,5S)-2,2-dimethyl-5-((E)-styryl)-1,3-dioxolan-4-yl)ethyl acetate
CAS NO:1246868-07-4
Molecular Formula:
Molecular Weight: 290.359
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: (R)-1-((4S,5S)-2,2-dimethyl-5-((E)-styryl)-1,3-dioxolan-4-yl)ethyl acetate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-1-((4S,5S)-2,2-dimethyl-5-((E)-styryl)-1,3-dioxolan-4-yl)ethyl acetate(1246868-07-4)
EPA Substance Registry System: (R)-1-((4S,5S)-2,2-dimethyl-5-((E)-styryl)-1,3-dioxolan-4-yl)ethyl acetate(1246868-07-4)

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: 1246868-07-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1246868-07-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,8,6 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1246868-07:
(9*1)+(8*2)+(7*4)+(6*6)+(5*8)+(4*6)+(3*8)+(2*0)+(1*7)=184
184 % 10 = 4
So 1246868-07-4 is a valid CAS Registry Number.

1246868-07-4Upstream product

108-05-4 vinyl acetate

1246868-07-4Downstream Products

1246868-07-4Relevant academic research and scientific papers

Oxygenated stereotriads with definite absolute configuration by lipase-mediated kinetic resolution: De novo synthesis of imino sugars and 6-deoxy- C-glycosides

Acctti, Daniela,Brenna, Elisabetta,Gatti, Francesco G.

experimental part, p. 4468 - 4475 (2010/10/02)

The lipase-mediated kinetic resolution of compound 1 was investigated, to prepare chiral synthons showing oxygenated stereotriads in a definite configurational arrangement. These key intermediates were embedded in biologically relevant structures, such as hydroxylated pyrrolidine 3 and C-phenyl glycosides by classical organic reactions.

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