Cas 62701-83-1,Acetic acid (1R,2S)-2-(2-acetoxy-4,6-dimethoxy-phenyl)-2-(4-acetoxy-phenyl)-1-(2,4-dimethoxy-6-methoxymethoxy-benzoyl)-ethyl ester

62701-83-1

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Basic information

Product Name: Acetic acid (1R,2S)-2-(2-acetoxy-4,6-dimethoxy-phenyl)-2-(4-acetoxy-phenyl)-1-(2,4-dimethoxy-6-methoxymethoxy-benzoyl)-ethyl ester
Synonyms:
CAS NO:62701-83-1
Molecular Formula:
Molecular Weight: 640.641
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: Acetic acid (1R,2S)-2-(2-acetoxy-4,6-dimethoxy-phenyl)-2-(4-acetoxy-phenyl)-1-(2,4-dimethoxy-6-methoxymethoxy-benzoyl)-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (1R,2S)-2-(2-acetoxy-4,6-dimethoxy-phenyl)-2-(4-acetoxy-phenyl)-1-(2,4-dimethoxy-6-methoxymethoxy-benzoyl)-ethyl ester(62701-83-1)
EPA Substance Registry System: Acetic acid (1R,2S)-2-(2-acetoxy-4,6-dimethoxy-phenyl)-2-(4-acetoxy-phenyl)-1-(2,4-dimethoxy-6-methoxymethoxy-benzoyl)-ethyl ester(62701-83-1)

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: 62701-83-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 62701-83-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,0 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62701-83:
(7*6)+(6*2)+(5*7)+(4*0)+(3*1)+(2*8)+(1*3)=111
111 % 10 = 1
So 62701-83-1 is a valid CAS Registry Number.

62701-83-1Upstream product

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62701-83-1Relevant academic research and scientific papers

Base-catalysed Acyloin Rearrangement: the First Synthesis of 4-Arylflavan-3-ones via Chalcone Epoxides

Hall, Alida J.,Ferreira, Daneel,Roux, David G.

, p. 1025 - 1028 (2007/10/02)

3,3-Diaryl-2-hydroxypropiophenones are amenable to base-catalysed α-ketol rearrangements yielding isomeric 1-hydroxypropan-2-ones.These structural isomers exhibit marked differences in oxidation potencial and serve as useful synthetic intermediates for no

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