Cas 187756-39-4,(4R,5R)-2-[(E)-6-(2,4-Dimethoxy-phenyl)-6-oxo-hex-1-enyl]-[1,3]dioxolane-4,5-dicarboxylic acid bis-dimethylamide

187756-39-4

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Basic information

Product Name: (4R,5R)-2-[(E)-6-(2,4-Dimethoxy-phenyl)-6-oxo-hex-1-enyl]-[1,3]dioxolane-4,5-dicarboxylic acid bis-dimethylamide
Synonyms: (4R,5R)-2-[(E)-6-(2,4-Dimethoxy-phenyl)-6-oxo-hex-1-enyl]-[1,3]dioxolane-4,5-dicarboxylic acid bis-dimethylamide
CAS NO:187756-39-4
Molecular Formula:
Molecular Weight: 448.516
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: (4R,5R)-2-[(E)-6-(2,4-Dimethoxy-phenyl)-6-oxo-hex-1-enyl]-[1,3]dioxolane-4,5-dicarboxylic acid bis-dimethylamide(CAS DataBase Reference)
NIST Chemistry Reference: (4R,5R)-2-[(E)-6-(2,4-Dimethoxy-phenyl)-6-oxo-hex-1-enyl]-[1,3]dioxolane-4,5-dicarboxylic acid bis-dimethylamide(187756-39-4)
EPA Substance Registry System: (4R,5R)-2-[(E)-6-(2,4-Dimethoxy-phenyl)-6-oxo-hex-1-enyl]-[1,3]dioxolane-4,5-dicarboxylic acid bis-dimethylamide(187756-39-4)

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: 187756-39-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 187756-39-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,7,5 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 187756-39:
(8*1)+(7*8)+(6*7)+(5*7)+(4*5)+(3*6)+(2*3)+(1*9)=194
194 % 10 = 4
So 187756-39-4 is a valid CAS Registry Number.

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187756-39-4Relevant academic research and scientific papers

Remote stereochemical control of both reacting centers in ketyl-olefin radical cyclizations: Involvement of a samarium tridentate ligate

Molander, Gary A.,McWilliams, J. Christopher,Noll, Bruce C.

, p. 1265 - 1276 (1997)

High diastereoselection in a samarium(II) iodide-promoted ketyl-olefin cyclization reaction has been achieved using tartramide-derived keto allylic acetals as chiral auxiliaries. The unique features of the reaction include the fact that remote diastereose

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