Cas 402856-26-2,Propanoic acid, 3-[bis(4-methoxyphenyl)phenylmethoxy]-2-(2-propenyloxy)-, methyl ester, (2R)-

402856-26-2

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Basic information

Product Name: Propanoic acid, 3-[bis(4-methoxyphenyl)phenylmethoxy]-2-(2-propenyloxy)-, methyl ester, (2R)-
Synonyms:
CAS NO:402856-26-2
Molecular Formula: C28H30O6
Molecular Weight: 462.543
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: Propanoic acid, 3-[bis(4-methoxyphenyl)phenylmethoxy]-2-(2-propenyloxy)-, methyl ester, (2R)-(CAS DataBase Reference)
NIST Chemistry Reference: Propanoic acid, 3-[bis(4-methoxyphenyl)phenylmethoxy]-2-(2-propenyloxy)-, methyl ester, (2R)-(402856-26-2)
EPA Substance Registry System: Propanoic acid, 3-[bis(4-methoxyphenyl)phenylmethoxy]-2-(2-propenyloxy)-, methyl ester, (2R)-(402856-26-2)

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: 402856-26-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 402856-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,2,8,5 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 402856-26:
(8*4)+(7*0)+(6*2)+(5*8)+(4*5)+(3*6)+(2*2)+(1*6)=132
132 % 10 = 2
So 402856-26-2 is a valid CAS Registry Number.

402856-26-2Upstream product

402856-26-2Downstream Products

606124-30-5 methyl (R)-3-O-(4,4'-dimethoxytrityl)-2-O-propargyl-glycerate

402856-26-2Relevant academic research and scientific papers

A cross metathesis-based synthesis of analogues of the 2-O-alkyl glycerate part of the moenomycins

Eichelberger, Uwe,Mansourova, Madina,Hennig, Lothar,Findeisen, Matthias,Giesa, Sabine,Müller, Dietrich,Welzel, Peter

, p. 9737 - 9742 (2007/10/03)

Conditions are reported which allow to convert optically active methyl glycerate to the 2-O-allyl derivative without racemization. Cross metathesis reactions then lead to analogues of the 2-O-alkyl glycerate part of the moenomycin antibiotics.

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