Cas 880462-49-7,(6E)-(2S,4R,5R)-8-ethoxycarbonyloxy-2-benzyloxy-4,6-dimethyl-5-hydroxy-6-octen-3-one

880462-49-7

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Basic information

Product Name: (6E)-(2S,4R,5R)-8-ethoxycarbonyloxy-2-benzyloxy-4,6-dimethyl-5-hydroxy-6-octen-3-one
Synonyms: (6E)-(2S,4R,5R)-8-ethoxycarbonyloxy-2-benzyloxy-4,6-dimethyl-5-hydroxy-6-octen-3-one
CAS NO:880462-49-7
Molecular Formula:
Molecular Weight: 364.439
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: (6E)-(2S,4R,5R)-8-ethoxycarbonyloxy-2-benzyloxy-4,6-dimethyl-5-hydroxy-6-octen-3-one(CAS DataBase Reference)
NIST Chemistry Reference: (6E)-(2S,4R,5R)-8-ethoxycarbonyloxy-2-benzyloxy-4,6-dimethyl-5-hydroxy-6-octen-3-one(880462-49-7)
EPA Substance Registry System: (6E)-(2S,4R,5R)-8-ethoxycarbonyloxy-2-benzyloxy-4,6-dimethyl-5-hydroxy-6-octen-3-one(880462-49-7)

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: 880462-49-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 880462-49-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,0,4,6 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 880462-49:
(8*8)+(7*8)+(6*0)+(5*4)+(4*6)+(3*2)+(2*4)+(1*9)=187
187 % 10 = 7
So 880462-49-7 is a valid CAS Registry Number.

880462-49-7Upstream product

880462-49-7Downstream Products

880462-50-0 (6E)-(2S,4R,5R)-8-ethoxycarbonyloxy-2-benzyloxy-4,6-dimethyl-5-tert-butyldimethylsiloxy-6-octen-3-one

880462-49-7Relevant academic research and scientific papers

Diastereoselective palladium-catalyzed formate reduction of allylic carbonates en route to polypropionate systems

Chau, Anh,Paquin, Jean-Francois,Lautens, Mark

, p. 1924 - 1933 (2007/10/03)

Diastereoselective palladium-catalyzed formate reduction of allylic carbonates presents unique opportunities for applications in target-oriented organic synthesis provided that selectivity, in particular stereoselectivity, in the course of this metal-cata

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