Cas 402856-10-4,Propanoic acid, 3-[bis(4-methoxyphenyl)phenylmethoxy]-2-[(2E)-2-heptadecenyloxy]-, methyl ester, (2S)-

402856-10-4

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Basic information

Product Name: Propanoic acid, 3-[bis(4-methoxyphenyl)phenylmethoxy]-2-[(2E)-2-heptadecenyloxy]-, methyl ester, (2S)-
Synonyms:
CAS NO:402856-10-4
Molecular Formula: C42H58O6
Molecular Weight: 658.919
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-[(2E)-2-heptadecenyloxy]-, methyl ester, (2S)-(CAS DataBase Reference)
NIST Chemistry Reference: Propanoic acid, 3-[bis(4-methoxyphenyl)phenylmethoxy]-2-[(2E)-2-heptadecenyloxy]-, methyl ester, (2S)-(402856-10-4)
EPA Substance Registry System: Propanoic acid, 3-[bis(4-methoxyphenyl)phenylmethoxy]-2-[(2E)-2-heptadecenyloxy]-, methyl ester, (2S)-(402856-10-4)

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: 402856-10-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 402856-10-4 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, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 402856-10:
(8*4)+(7*0)+(6*2)+(5*8)+(4*5)+(3*6)+(2*1)+(1*0)=124
124 % 10 = 4
So 402856-10-4 is a valid CAS Registry Number.

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402856-10-4Relevant 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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