Cas 1265223-71-9,(4R,5R)-4-((2R,3R,4R)-3-(benzyloxy)-4-methylhexan-2-yl)-2,2,5-trimethyl-1,3-dioxane

1265223-71-9

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Basic information

Product Name: (4R,5R)-4-((2R,3R,4R)-3-(benzyloxy)-4-methylhexan-2-yl)-2,2,5-trimethyl-1,3-dioxane
Synonyms: (4R,5R)-4-((2R,3R,4R)-3-(benzyloxy)-4-methylhexan-2-yl)-2,2,5-trimethyl-1,3-dioxane
CAS NO:1265223-71-9
Molecular Formula:
Molecular Weight: 334.499
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)-4-((2R,3R,4R)-3-(benzyloxy)-4-methylhexan-2-yl)-2,2,5-trimethyl-1,3-dioxane(CAS DataBase Reference)
NIST Chemistry Reference: (4R,5R)-4-((2R,3R,4R)-3-(benzyloxy)-4-methylhexan-2-yl)-2,2,5-trimethyl-1,3-dioxane(1265223-71-9)
EPA Substance Registry System: (4R,5R)-4-((2R,3R,4R)-3-(benzyloxy)-4-methylhexan-2-yl)-2,2,5-trimethyl-1,3-dioxane(1265223-71-9)

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: 1265223-71-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1265223-71-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,5,2,2 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1265223-71:
(9*1)+(8*2)+(7*6)+(6*5)+(5*2)+(4*2)+(3*3)+(2*7)+(1*1)=139
139 % 10 = 9
So 1265223-71-9 is a valid CAS Registry Number.

1265223-71-9Upstream product

1265223-71-9Downstream Products

1265223-71-9Relevant academic research and scientific papers

Total synthesis of (+)-bourgeanic acid utilizing desymmetrization strategy

Yadav, Jhillu S.,Rao, K. V. Raghavendra,Ravindar,Reddy, B. V. Subba

, p. 58 - 61 (2011)

A highly stereoselective total synthesis of an aliphatic depside (+)-bourgeanic acid via (-)-hemibourgeanic acid and bourgeanic lactone is described. The key steps involved in this synthesis are desymmetrization of bicyclic olefin with Brown's asymmetric

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