Cas 1046789-85-8,4-(2-ethynyl-5-methoxyphenyl)-2-methylenebutyl (1S,2R,5S)-2-isopropyl-5-methylcyclohexyl carbonate

1046789-85-8

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Basic information

Product Name: 4-(2-ethynyl-5-methoxyphenyl)-2-methylenebutyl (1S,2R,5S)-2-isopropyl-5-methylcyclohexyl carbonate
Synonyms: 4-(2-ethynyl-5-methoxyphenyl)-2-methylenebutyl (1S,2R,5S)-2-isopropyl-5-methylcyclohexyl carbonate
CAS NO:1046789-85-8
Molecular Formula:
Molecular Weight: 398.543
EINECS: N/A
Product Categories: N/A
Mol File: 1046789-85-8.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: 4-(2-ethynyl-5-methoxyphenyl)-2-methylenebutyl (1S,2R,5S)-2-isopropyl-5-methylcyclohexyl carbonate(CAS DataBase Reference)
NIST Chemistry Reference: 4-(2-ethynyl-5-methoxyphenyl)-2-methylenebutyl (1S,2R,5S)-2-isopropyl-5-methylcyclohexyl carbonate(1046789-85-8)
EPA Substance Registry System: 4-(2-ethynyl-5-methoxyphenyl)-2-methylenebutyl (1S,2R,5S)-2-isopropyl-5-methylcyclohexyl carbonate(1046789-85-8)

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: 1046789-85-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1046789-85-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,6,7,8 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1046789-85:
(9*1)+(8*0)+(7*4)+(6*6)+(5*7)+(4*8)+(3*9)+(2*8)+(1*5)=188
188 % 10 = 8
So 1046789-85-8 is a valid CAS Registry Number.

1046789-85-8Upstream product

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1046789-85-8Relevant articles and documents

Construction of quaternary centres for natural polycycles: The Pauson-Khand approach

Arnáiz, Eduardo,Blanco-Urgoiti, Jaime,Abdi, Delbrin,Domínguez, Gema,Castells, Javier Pérez

, p. 2431 - 2437 (2008/09/20)

Construction of quaternary carbons is a challenge in PK chemistry, with few precedents in the literature. Starting from suitable functionalized enynes including an aromatic ring that templates the reaction, polycyclic ketones are obtained with a quaternar

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