Cas 374087-95-3,(R)-(2-Methoxy-ethoxymethoxy)-phenyl-acetic acid (R)-1-methyl-2-oxo-ethyl ester

374087-95-3

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Basic information

Product Name: (R)-(2-Methoxy-ethoxymethoxy)-phenyl-acetic acid (R)-1-methyl-2-oxo-ethyl ester
Synonyms: (R)-(2-Methoxy-ethoxymethoxy)-phenyl-acetic acid (R)-1-methyl-2-oxo-ethyl ester
CAS NO:374087-95-3
Molecular Formula:
Molecular Weight: 296.32
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)-(2-Methoxy-ethoxymethoxy)-phenyl-acetic acid (R)-1-methyl-2-oxo-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-(2-Methoxy-ethoxymethoxy)-phenyl-acetic acid (R)-1-methyl-2-oxo-ethyl ester(374087-95-3)
EPA Substance Registry System: (R)-(2-Methoxy-ethoxymethoxy)-phenyl-acetic acid (R)-1-methyl-2-oxo-ethyl ester(374087-95-3)

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: 374087-95-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 374087-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,4,0,8 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 374087-95:
(8*3)+(7*7)+(6*4)+(5*0)+(4*8)+(3*7)+(2*9)+(1*5)=173
173 % 10 = 3
So 374087-95-3 is a valid CAS Registry Number.

374087-95-3Upstream product

19967-57-8 bromo-2 propanal

374087-95-3Downstream Products

374087-95-3Relevant academic research and scientific papers

Enantioselective synthesis of ancepsenolide and its analogs

Takai, Katsuki,Iriye, Ryozo

, p. 1903 - 1906 (2001)

Ancepsenolide (1a-s) and the enantiomer (1a-r) were respectively synthesized from (S)-and (R)-2-[(R)-O-MEM-mandeloyloxylpropanal (3a-s and 3a-r) and diisopropyl hexadecanedioate (5). The analogs (1b, 2a and 2b) were synthesized by a similar method.

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