Cas 204981-52-2,(3S,4R)-dicyclohexylammonium-2-(3-benzyl-4-hydroxy-3,4-dihydrobenzopyran-7-yl)-4-trifluoromethyl-benzoate

204981-52-2

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Basic information

Product Name: (3S,4R)-dicyclohexylammonium-2-(3-benzyl-4-hydroxy-3,4-dihydrobenzopyran-7-yl)-4-trifluoromethyl-benzoate
Synonyms: (3S,4R)-dicyclohexylammonium-2-(3-benzyl-4-hydroxy-3,4-dihydrobenzopyran-7-yl)-4-trifluoromethyl-benzoate
CAS NO:204981-52-2
Molecular Formula:
Molecular Weight: 609.729
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: (3S,4R)-dicyclohexylammonium-2-(3-benzyl-4-hydroxy-3,4-dihydrobenzopyran-7-yl)-4-trifluoromethyl-benzoate(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4R)-dicyclohexylammonium-2-(3-benzyl-4-hydroxy-3,4-dihydrobenzopyran-7-yl)-4-trifluoromethyl-benzoate(204981-52-2)
EPA Substance Registry System: (3S,4R)-dicyclohexylammonium-2-(3-benzyl-4-hydroxy-3,4-dihydrobenzopyran-7-yl)-4-trifluoromethyl-benzoate(204981-52-2)

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: 204981-52-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 204981-52-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,9,8 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 204981-52:
(8*2)+(7*0)+(6*4)+(5*9)+(4*8)+(3*1)+(2*5)+(1*2)=132
132 % 10 = 2
So 204981-52-2 is a valid CAS Registry Number.

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204981-52-2Relevant academic research and scientific papers

Benzoic acid substituted benzopyrans for the treatment of atherosclerosis

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, (2008/06/13)

A method of treating atherosclerosis in a mammal, including a human, comprising administering to said mammal an amount of the compound of the formula an enantiomer, or the pharmaceutically acceptable salt thereof; effective to treat atherosclerosis, where

Processes for preparing substituted chromanol derivatives

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, (2008/06/13)

PCT No. PCT/IB97/01024 Sec. 371 Date Mar. 5, 1999 Sec. 102(e) Date Mar. 5, 1999 PCT Filed Aug. 25, 1997 PCT Pub. No. WO98/11085 PCT Pub. Date Mar. 19, 1998The invention relates to processes for preparing a compound of the formula (X) and the enantiomer of

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