Cas 274263-53-5,(2S,6S,7S,8S)-8-(4-Methoxy-benzyloxy)-6-methoxymethoxy-2,7-dimethyl-3-oxo-decanoic acid methoxy-methyl-amide

274263-53-5

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Basic information

Product Name: (2S,6S,7S,8S)-8-(4-Methoxy-benzyloxy)-6-methoxymethoxy-2,7-dimethyl-3-oxo-decanoic acid methoxy-methyl-amide
Synonyms:
CAS NO:274263-53-5
Molecular Formula:
Molecular Weight: 453.576
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: (2S,6S,7S,8S)-8-(4-Methoxy-benzyloxy)-6-methoxymethoxy-2,7-dimethyl-3-oxo-decanoic acid methoxy-methyl-amide(CAS DataBase Reference)
NIST Chemistry Reference: (2S,6S,7S,8S)-8-(4-Methoxy-benzyloxy)-6-methoxymethoxy-2,7-dimethyl-3-oxo-decanoic acid methoxy-methyl-amide(274263-53-5)
EPA Substance Registry System: (2S,6S,7S,8S)-8-(4-Methoxy-benzyloxy)-6-methoxymethoxy-2,7-dimethyl-3-oxo-decanoic acid methoxy-methyl-amide(274263-53-5)

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: 274263-53-5(Hazardous Substances Data)

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274263-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 274263-53-5 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 274263-53:
(8*2)+(7*7)+(6*4)+(5*2)+(4*6)+(3*3)+(2*5)+(1*3)=145
145 % 10 = 5
So 274263-53-5 is a valid CAS Registry Number.

274263-53-5Upstream product

274263-53-5Downstream Products

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

274263-53-5Relevant 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 (2000)

(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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