Cas 848138-66-9,(1R,5R,6S)-6-(4-hydroxy-3,5-dimethoxyphenyl)-5-hydroxymethyl-8-oxabicyclo[3.2.1]oct-3-en-2-one

848138-66-9

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Basic information

Product Name: (1R,5R,6S)-6-(4-hydroxy-3,5-dimethoxyphenyl)-5-hydroxymethyl-8-oxabicyclo[3.2.1]oct-3-en-2-one
Synonyms:
CAS NO:848138-66-9
Molecular Formula:
Molecular Weight: 306.315
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,5R,6S)-6-(4-hydroxy-3,5-dimethoxyphenyl)-5-hydroxymethyl-8-oxabicyclo[3.2.1]oct-3-en-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (1R,5R,6S)-6-(4-hydroxy-3,5-dimethoxyphenyl)-5-hydroxymethyl-8-oxabicyclo[3.2.1]oct-3-en-2-one(848138-66-9)
EPA Substance Registry System: (1R,5R,6S)-6-(4-hydroxy-3,5-dimethoxyphenyl)-5-hydroxymethyl-8-oxabicyclo[3.2.1]oct-3-en-2-one(848138-66-9)

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: 848138-66-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 848138-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,1,3 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 848138-66:
(8*8)+(7*4)+(6*8)+(5*1)+(4*3)+(3*8)+(2*6)+(1*6)=199
199 % 10 = 9
So 848138-66-9 is a valid CAS Registry Number.

848138-66-9Upstream product

848138-66-9Downstream Products

848138-66-9Relevant academic research and scientific papers

Catalytic asymmetric synthesis of descurainin via 1, 3-dipolar cycloaddition of a carbonyl ylide using Rh2(R-TCPTTL)4

Shimada, Naoyuki,Hanari, Taiki,Kurosaki, Yasunobu,Anada, Masahiro,Nambu, Hisanori,Hashimoto, Shunichi

, p. 6572 - 6575 (2010)

A catalytic asymmetric synthesis of descurainin has been achieved by incorporating an enantioselective 1,3-dipolar cycloaddition, a stereoselective alkene hydrogénation, an oxidation with Fremy's salt and a regioselective demethylation with NbCl5/su

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