Cas 274263-54-6,Methanesulfonic acid (1S,4S,5S,6S)-6-(4-methoxy-benzyloxy)-4-methoxymethoxy-1-[(S)-1-(methoxy-methyl-carbamoyl)-ethyl]-5-methyl-octyl ester

274263-54-6

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Basic information

Product Name: Methanesulfonic acid (1S,4S,5S,6S)-6-(4-methoxy-benzyloxy)-4-methoxymethoxy-1-[(S)-1-(methoxy-methyl-carbamoyl)-ethyl]-5-methyl-octyl ester
Synonyms:
CAS NO:274263-54-6
Molecular Formula:
Molecular Weight: 533.684
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: Methanesulfonic acid (1S,4S,5S,6S)-6-(4-methoxy-benzyloxy)-4-methoxymethoxy-1-[(S)-1-(methoxy-methyl-carbamoyl)-ethyl]-5-methyl-octyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Methanesulfonic acid (1S,4S,5S,6S)-6-(4-methoxy-benzyloxy)-4-methoxymethoxy-1-[(S)-1-(methoxy-methyl-carbamoyl)-ethyl]-5-methyl-octyl ester(274263-54-6)
EPA Substance Registry System: Methanesulfonic acid (1S,4S,5S,6S)-6-(4-methoxy-benzyloxy)-4-methoxymethoxy-1-[(S)-1-(methoxy-methyl-carbamoyl)-ethyl]-5-methyl-octyl ester(274263-54-6)

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: 274263-54-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 274263-54-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,4,2,6 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 274263-54:
(8*2)+(7*7)+(6*4)+(5*2)+(4*6)+(3*3)+(2*5)+(1*4)=146
146 % 10 = 6
So 274263-54-6 is a valid CAS Registry Number.

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274263-54-6Relevant academic research and scientific papers

Catalytic, Asymmetric Synthesis of the C1′-C10′ Segment of Pamamycin 621A

Calter, Michael A.,Bi, F. Christopher

, p. 1529 - 1531 (2007/10/03)

(Equation Presented) This paper describes a catalytic, asymmetric approach to the C1′-C10′ segment of pamamycin 621A. We synthesize this segment in a convergent manner, with each of the coupling partners ultimately deriving from enantiomerically enriched methylketene dimer.

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