Cas 240116-14-7,2-[(E)-3-((2R,3S,4S,5R,6S)-4-Benzyloxy-6-methoxy-3,5-dimethyl-tetrahydro-pyran-2-yl)-propenyl]-5-methoxy-oxazole-4-carboxylic acid methyl ester

240116-14-7

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Basic information

Product Name: 2-[(E)-3-((2R,3S,4S,5R,6S)-4-Benzyloxy-6-methoxy-3,5-dimethyl-tetrahydro-pyran-2-yl)-propenyl]-5-methoxy-oxazole-4-carboxylic acid methyl ester
Synonyms: 2-[(E)-3-((2R,3S,4S,5R,6S)-4-Benzyloxy-6-methoxy-3,5-dimethyl-tetrahydro-pyran-2-yl)-propenyl]-5-methoxy-oxazole-4-carboxylic acid methyl ester
CAS NO:240116-14-7
Molecular Formula:
Molecular Weight: 445.513
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: 2-[(E)-3-((2R,3S,4S,5R,6S)-4-Benzyloxy-6-methoxy-3,5-dimethyl-tetrahydro-pyran-2-yl)-propenyl]-5-methoxy-oxazole-4-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(E)-3-((2R,3S,4S,5R,6S)-4-Benzyloxy-6-methoxy-3,5-dimethyl-tetrahydro-pyran-2-yl)-propenyl]-5-methoxy-oxazole-4-carboxylic acid methyl ester(240116-14-7)
EPA Substance Registry System: 2-[(E)-3-((2R,3S,4S,5R,6S)-4-Benzyloxy-6-methoxy-3,5-dimethyl-tetrahydro-pyran-2-yl)-propenyl]-5-methoxy-oxazole-4-carboxylic acid methyl ester(240116-14-7)

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: 240116-14-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 240116-14-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,0,1,1 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 240116-14:
(8*2)+(7*4)+(6*0)+(5*1)+(4*1)+(3*6)+(2*1)+(1*4)=77
77 % 10 = 7
So 240116-14-7 is a valid CAS Registry Number.

240116-14-7Upstream product

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240116-14-7Relevant academic research and scientific papers

Synthesis of the enantiopure C15-C26 segment of phorboxazole A and B

Wolbers, Peter,Misske, Andrea M.,Hoffmann, H. Martin R.

, p. 4527 - 4530 (2007/10/03)

Two approaches towards an enantiopure C15-C26 segment of the phorboxazoles starting from the corresponding C20-C26 aldehyde are presented. A variety of functionalized oxazoles have been synthesized via the rhodium(II) acetate catalyzed cycloaddition of dimethyl diazomalonate to substituted nitriles.

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