Cas 1294481-75-6,7,4'-(R)-(-)-α-methoxy-α-(trifluoromethyl)phenylacetoxy pentacecilide C

1294481-75-6

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Basic information

Product Name: 7,4'-(R)-(-)-α-methoxy-α-(trifluoromethyl)phenylacetoxy pentacecilide C
Synonyms: 7,4'-(R)-(-)-α-methoxy-α-(trifluoromethyl)phenylacetoxy pentacecilide C
CAS NO:1294481-75-6
Molecular Formula:
Molecular Weight: 918.881
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: 7,4'-(R)-(-)-α-methoxy-α-(trifluoromethyl)phenylacetoxy pentacecilide C(CAS DataBase Reference)
NIST Chemistry Reference: 7,4'-(R)-(-)-α-methoxy-α-(trifluoromethyl)phenylacetoxy pentacecilide C(1294481-75-6)
EPA Substance Registry System: 7,4'-(R)-(-)-α-methoxy-α-(trifluoromethyl)phenylacetoxy pentacecilide C(1294481-75-6)

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: 1294481-75-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1294481-75-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,4,4,8 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1294481-75:
(9*1)+(8*2)+(7*9)+(6*4)+(5*4)+(4*8)+(3*1)+(2*7)+(1*5)=186
186 % 10 = 6
So 1294481-75-6 is a valid CAS Registry Number.

1294481-75-6Upstream product

39637-99-5 (S)-(+)-2-methoxy-2-trifluoromethyl-2-phenylacetyl chloride

1294481-75-6Downstream Products

1294481-75-6Relevant academic research and scientific papers

Absolute stereochemistry of pentacecilides, new inhibitors of lipid droplet formation in mouse macrophages, produced by Penicillium cecidicola FKI-3765-1

Yamazaki, Hiroyuki,Ugaki, Narihiro,Matsuda, Daisuke,Tomoda, Hiroshi

, p. 315 - 318 (2010)

The structure of a new pentacecilide congener, pentacecilide D, produced by Penicillium cecidicola FKI-3765-1 was elucidated by various NMR experiments. The absolute stereochemistry of pentacecilides was elucidated by using the modified Mosher method for

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