Cas 1352007-47-6,(R)-4-benzyl-3-((R)-2,3-bis(4-methoxyphenyl)propanoyl)oxazolidin-2-one

1352007-47-6

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Basic information

Product Name: (R)-4-benzyl-3-((R)-2,3-bis(4-methoxyphenyl)propanoyl)oxazolidin-2-one
Synonyms: (R)-4-benzyl-3-((R)-2,3-bis(4-methoxyphenyl)propanoyl)oxazolidin-2-one
CAS NO:1352007-47-6
Molecular Formula:
Molecular Weight: 445.515
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: (R)-4-benzyl-3-((R)-2,3-bis(4-methoxyphenyl)propanoyl)oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (R)-4-benzyl-3-((R)-2,3-bis(4-methoxyphenyl)propanoyl)oxazolidin-2-one(1352007-47-6)
EPA Substance Registry System: (R)-4-benzyl-3-((R)-2,3-bis(4-methoxyphenyl)propanoyl)oxazolidin-2-one(1352007-47-6)

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: 1352007-47-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1352007-47-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,0,0 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1352007-47:
(9*1)+(8*3)+(7*5)+(6*2)+(5*0)+(4*0)+(3*7)+(2*4)+(1*7)=116
116 % 10 = 6
So 1352007-47-6 is a valid CAS Registry Number.

1352007-47-6Upstream product

1352007-47-6Downstream Products

524047-78-7 (R)-DPN

1352007-47-6Relevant academic research and scientific papers

Diarylpropionitrile (DPN) enantiomers: Synthesis and evaluation of estrogen receptor β-selective ligands

Carroll, Vincent M.,Jeyakumar,Carlson, Kathryn E.,Katzenellenbogen, John A.

, p. 528 - 537 (2012)

Two estrogen receptor (ER) subtypes, ERα and ERβ, mediate the actions of estrogens in diverse reproductive and nonreproductive target tissues. ER subtype-selective ligands, which bind to and activate these subtypes differentially, have proved to be useful

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