Cas 894422-95-8,6-acetoxy-3-hydroxy-5-methyl-biphenyl-2-carboxylic acid methyl ester

894422-95-8

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Basic information

Product Name: 6-acetoxy-3-hydroxy-5-methyl-biphenyl-2-carboxylic acid methyl ester
Synonyms:
CAS NO:894422-95-8
Molecular Formula:
Molecular Weight: 300.311
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: 6-acetoxy-3-hydroxy-5-methyl-biphenyl-2-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 6-acetoxy-3-hydroxy-5-methyl-biphenyl-2-carboxylic acid methyl ester(894422-95-8)
EPA Substance Registry System: 6-acetoxy-3-hydroxy-5-methyl-biphenyl-2-carboxylic acid methyl ester(894422-95-8)

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: 894422-95-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 894422-95-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,4,4,2 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 894422-95:
(8*8)+(7*9)+(6*4)+(5*4)+(4*2)+(3*2)+(2*9)+(1*5)=208
208 % 10 = 8
So 894422-95-8 is a valid CAS Registry Number.

894422-95-8Upstream product

74590-73-1 1,3-bis(trimethylsiloxy)-1-methoxybuta-1,3-diene

894422-95-8Downstream Products

894422-95-8Relevant academic research and scientific papers

Synthesis of functionalized p-dihydrobenzoquinones and p-benzoquinones based on [3+3] cyclizations of 1,3-bis-silyl enol ethers

Ahmed, Zafar,Fischer, Christine,Spannenberg, Anke,Langer, Peter

, p. 4800 - 4806 (2006)

Functionalized mono-protected p-dihydrobenzoquinones were prepared by [3+3] cyclization of 1,3-bis-silyl enol ethers with 2-acyloxy-3-(silyloxy)alk-2-en-1-ones. Deprotection and oxidation of the products afforded the corresponding p-benzoquinones.

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