Cas 1160726-17-9,6-bromo-3-(p-benzyloxyphenyl)-1,2,4,5-tetrakis((methoxy)methoxy)benzene

1160726-17-9

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Basic information

Product Name: 6-bromo-3-(p-benzyloxyphenyl)-1,2,4,5-tetrakis((methoxy)methoxy)benzene
Synonyms: 6-bromo-3-(p-benzyloxyphenyl)-1,2,4,5-tetrakis((methoxy)methoxy)benzene
CAS NO:1160726-17-9
Molecular Formula:
Molecular Weight: 579.442
EINECS: N/A
Product Categories: N/A
Mol File: 1160726-17-9.mol
Article Data: 1

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: 6-bromo-3-(p-benzyloxyphenyl)-1,2,4,5-tetrakis((methoxy)methoxy)benzene(CAS DataBase Reference)
NIST Chemistry Reference: 6-bromo-3-(p-benzyloxyphenyl)-1,2,4,5-tetrakis((methoxy)methoxy)benzene(1160726-17-9)
EPA Substance Registry System: 6-bromo-3-(p-benzyloxyphenyl)-1,2,4,5-tetrakis((methoxy)methoxy)benzene(1160726-17-9)

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: 1160726-17-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1160726-17-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,7,2 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1160726-17:
(9*1)+(8*1)+(7*6)+(6*0)+(5*7)+(4*2)+(3*6)+(2*1)+(1*7)=129
129 % 10 = 9
So 1160726-17-9 is a valid CAS Registry Number.

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1160726-17-9Relevant articles and documents

Structural revision of thelephantin G by total synthesis and the inhibitory activity against TNF-α production

Yue, Qi Ye,Koshino, Hiroyuki,Onose, Jun-Ichi,Negishi, Chiemi,Yoshikawa, Kunie,Abe, Naoki,Takahashi, Shunya

experimental part, p. 4642 - 4645 (2009/09/25)

(Chemical Equation Presented) This paper describes the total synthesis of thelephantin G, thus revising the proposed structure 1 to 2. The key steps involved a double Suzuki-Miyaura coupling and an esteri-fication reaction. By a similar strategy, ganbajun

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