Cas 141476-35-9,2(3H)-Isoquinolinecarboxylic acid, 4,4a,5,6,7,8-hexahydro-4a-(3-methoxyphenyl)-, 2,2,2-trichloroethyl ester

141476-35-9

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Basic information

Product Name: 2(3H)-Isoquinolinecarboxylic acid, 4,4a,5,6,7,8-hexahydro-4a-(3-methoxyphenyl)-, 2,2,2-trichloroethyl ester
Synonyms:
CAS NO:141476-35-9
Molecular Formula: C19H22Cl3NO3
Molecular Weight: 418.748
EINECS: N/A
Product Categories: N/A
Mol File: 141476-35-9.mol

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: 2(3H)-Isoquinolinecarboxylic acid, 4,4a,5,6,7,8-hexahydro-4a-(3-methoxyphenyl)-, 2,2,2-trichloroethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2(3H)-Isoquinolinecarboxylic acid, 4,4a,5,6,7,8-hexahydro-4a-(3-methoxyphenyl)-, 2,2,2-trichloroethyl ester(141476-35-9)
EPA Substance Registry System: 2(3H)-Isoquinolinecarboxylic acid, 4,4a,5,6,7,8-hexahydro-4a-(3-methoxyphenyl)-, 2,2,2-trichloroethyl ester(141476-35-9)

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: 141476-35-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141476-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,4,7 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141476-35:
(8*1)+(7*4)+(6*1)+(5*4)+(4*7)+(3*6)+(2*3)+(1*5)=119
119 % 10 = 9
So 141476-35-9 is a valid CAS Registry Number.

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141476-35-9Relevant academic research and scientific papers

Establishment of efficient hydroxylation at angular position of 4a-aryl-trans-decahydro-isoquinolines

Kawai, Koji,Kawamura, Kuniaki,Nagase, Hiroshi

, p. 949 - 959 (2007/10/03)

Efficient hydroxylation method at angular 8a position of 4a-aryl-trans-decahydroisoquinolines was described. By utilizing the transformation process, syntheses of 2-methyl- and 2-cyclopropylmethyl-8a-hydroxy-4a-(3-methoxyphenyl)-6-oxo-trans- decahydroisoq

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