Cas 165449-25-2,(1R,3R,4S)-8-phenyl-p-menthan-3-yl (2'S)-2'benzyl-2'-fluoro-3'-(p-methoxybenzyloxy)propionate

165449-25-2

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Basic information

Product Name: (1R,3R,4S)-8-phenyl-p-menthan-3-yl (2'S)-2'benzyl-2'-fluoro-3'-(p-methoxybenzyloxy)propionate
Synonyms:
CAS NO:165449-25-2
Molecular Formula:
Molecular Weight: 532.696
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: (1R,3R,4S)-8-phenyl-p-menthan-3-yl (2'S)-2'benzyl-2'-fluoro-3'-(p-methoxybenzyloxy)propionate(CAS DataBase Reference)
NIST Chemistry Reference: (1R,3R,4S)-8-phenyl-p-menthan-3-yl (2'S)-2'benzyl-2'-fluoro-3'-(p-methoxybenzyloxy)propionate(165449-25-2)
EPA Substance Registry System: (1R,3R,4S)-8-phenyl-p-menthan-3-yl (2'S)-2'benzyl-2'-fluoro-3'-(p-methoxybenzyloxy)propionate(165449-25-2)

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: 165449-25-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 165449-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,4,4 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 165449-25:
(8*1)+(7*6)+(6*5)+(5*4)+(4*4)+(3*9)+(2*2)+(1*5)=152
152 % 10 = 2
So 165449-25-2 is a valid CAS Registry Number.

165449-25-2Upstream product

89238-99-3 O-(4-methoxybenzyl)-trichloroacetimidate

165449-25-2Downstream Products

162252-06-4 (2R)-2-benzyl-2-fluoro-3-(p-methoxybenzyloxy)-1-propanol

165449-25-2Relevant academic research and scientific papers

Enantiocontrolled synthesis of chiral propane-1,3-diol derivatives possessing fluorinated quaternary stereogenic centers

Ihara,Kawabuchi,Tokunaga,Fukumoto

, p. 1041 - 1050 (2007/10/02)

A general method for the preparation of chiral propane-1,3-diol derivatives possessing fluorinated quaternary stereogenic centers was established as follows. The diastereoselective alkylation of (1R,3R,4S)-8-phenylmenthyl hydrogen fluoromalonate 9, follow

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