Cas 1355955-89-3,3-[((4bS,8R,8aR)-2-isopropyl-8-(methoxycarbonyl)-4b,8-dimethyl-4b,5,6,7,8,8a,9,10-octahydrophenanthren-3-yl)methyl]-1-mesityl-3H-imidazol-1-ium chloride

1355955-89-3

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Basic information

Product Name: 3-[((4bS,8R,8aR)-2-isopropyl-8-(methoxycarbonyl)-4b,8-dimethyl-4b,5,6,7,8,8a,9,10-octahydrophenanthren-3-yl)methyl]-1-mesityl-3H-imidazol-1-ium chloride
Synonyms:
CAS NO:1355955-89-3
Molecular Formula:
Molecular Weight: 549.197
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: 3-[((4bS,8R,8aR)-2-isopropyl-8-(methoxycarbonyl)-4b,8-dimethyl-4b,5,6,7,8,8a,9,10-octahydrophenanthren-3-yl)methyl]-1-mesityl-3H-imidazol-1-ium chloride(CAS DataBase Reference)
NIST Chemistry Reference: 3-[((4bS,8R,8aR)-2-isopropyl-8-(methoxycarbonyl)-4b,8-dimethyl-4b,5,6,7,8,8a,9,10-octahydrophenanthren-3-yl)methyl]-1-mesityl-3H-imidazol-1-ium chloride(1355955-89-3)
EPA Substance Registry System: 3-[((4bS,8R,8aR)-2-isopropyl-8-(methoxycarbonyl)-4b,8-dimethyl-4b,5,6,7,8,8a,9,10-octahydrophenanthren-3-yl)methyl]-1-mesityl-3H-imidazol-1-ium chloride(1355955-89-3)

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: 1355955-89-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1355955-89-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,5,9,5 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1355955-89:
(9*1)+(8*3)+(7*5)+(6*5)+(5*9)+(4*5)+(3*5)+(2*8)+(1*9)=203
203 % 10 = 3
So 1355955-89-3 is a valid CAS Registry Number.

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1355955-89-3Relevant academic research and scientific papers

N-heterocyclic carbenes. IV.1synthesis of symmetrical and unsymmetrical imidazolium salts with abietane moiety

Glushkov,Arapov,Kotelev,Rudowsky,Suponitsky,Gorbunov,Maiorova,Slepukhin

experimental part, p. 5 - 15 (2012/03/27)

Methyl 12-chloromethyl-dehydroabie-tate reacts with 1-benzyl- and 1-arylimidazoles to give unsymmetrically substituted imidazolium chlorides (1a-i), with abietane moiety. Starting from methyl 12-aminodehydroabietate, symmetrically substituted diterpene-ba

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