Cas 1426084-55-0,(R)-2-(1-(ethoxycarbonyl)-5,5-dimethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-4-methyl-4,5-dihydrofuran-3-carboxylic acid

1426084-55-0

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Basic information

Product Name: (R)-2-(1-(ethoxycarbonyl)-5,5-dimethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-4-methyl-4,5-dihydrofuran-3-carboxylic acid
Synonyms:
CAS NO:1426084-55-0
Molecular Formula:
Molecular Weight: 358.434
EINECS: N/A
Product Categories: N/A
Mol File: 1426084-55-0.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: (R)-2-(1-(ethoxycarbonyl)-5,5-dimethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-4-methyl-4,5-dihydrofuran-3-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-(1-(ethoxycarbonyl)-5,5-dimethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-4-methyl-4,5-dihydrofuran-3-carboxylic acid(1426084-55-0)
EPA Substance Registry System: (R)-2-(1-(ethoxycarbonyl)-5,5-dimethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-4-methyl-4,5-dihydrofuran-3-carboxylic acid(1426084-55-0)

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: 1426084-55-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1426084-55-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,6,0,8 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1426084-55:
(9*1)+(8*4)+(7*2)+(6*6)+(5*0)+(4*8)+(3*4)+(2*5)+(1*5)=150
150 % 10 = 0
So 1426084-55-0 is a valid CAS Registry Number.

1426084-55-0Upstream product

35825-57-1 Cryptotanshinone

1426084-55-0Downstream Products

1426084-55-0Relevant articles and documents

Oxygen insertion of o-quinone under catalytic hydrogenation conditions

Zhang, Da-Li,Zhou, Li-Yan,Quan, Jun-Min,Zhang, Wei,Gu, Lian-Quan,Huang, Zhi-Shu,An, Lin-Kun

, p. 1162 - 1165 (2013)

An oxygen-insertion reaction that transforms an o-quinone and a conjugated α-diketone substrate into an anhydride product or derivative under catalytic hydrogenation conditions is reported. The experiments and computations indicate that the oxygen insertion proceeds via a radical mechanism mediated by an acetoxyl radical.

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