63490-92-6 Usage
Uses
Used in Pharmaceutical Industry:
(Z)-3,4-Dihydro-1-(2-hydroxy-3,4-dimethoxybenzylidene)-6,7-dimethoxyisoquinoline-2(1H)-carbaldehyde is used as a pharmaceutical compound for its potential therapeutic applications. (Z)-3,4-Dihydro-1-(2-hydroxy-3,4-dimethoxybenzylidene)-6,7-dimethoxyisoquinoline-2(1H)-carbaldehyde's unique structure and optical properties make it a candidate for the development of new drugs, particularly in the treatment of various diseases and disorders.
Used in Chemical Research:
In the field of chemical research, (Z)-3,4-Dihydro-1-(2-hydroxy-3,4-dimethoxybenzylidene)-6,7-dimethoxyisoquinoline-2(1H)-carbaldehyde serves as a valuable subject for studying the properties and reactivity of benzylisoquinoline alkaloids. Its synthesis, structural analysis, and potential reactions with other molecules can provide insights into the broader class of isoquinoline alkaloids and their applications in various industries.
Used in Material Science:
(Z)-3,4-Dihydro-1-(2-hydroxy-3,4-dimethoxybenzylidene)-6,7-dimethoxyisoquinoline-2(1H)-carbaldehyde may also find applications in material science due to its unique optical properties. (Z)-3,4-Dihydro-1-(2-hydroxy-3,4-dimethoxybenzylidene)-6,7-dimethoxyisoquinoline-2(1H)-carbaldehyde's absorption maxima in the ultraviolet spectrum suggest potential uses in the development of materials with specific light-absorbing or light-emitting characteristics, which could be beneficial in various technological applications, such as sensors or optoelectronic devices.
Used in Analytical Chemistry:
(Z)-3,4-Dihydro-1-(2-hydroxy-3,4-dimethoxybenzylidene)-6,7-dimethoxyisoquinoline-2(1H)-carbaldehyde's distinct ultraviolet spectrum can be utilized in analytical chemistry for the identification and quantification of similar compounds in complex mixtures. By employing techniques such as high-performance liquid chromatography (HPLC) or ultra-performance liquid chromatography (UPLC) coupled with UV-Vis detection, researchers can accurately analyze and characterize samples containing (Z)-3,4-Dihydro-1-(2-hydroxy-3,4-dimethoxybenzylidene)-6,7-dimethoxyisoquinoline-2(1H)-carbaldehyde and related alkaloids.
Check Digit Verification of cas no
The CAS Registry Mumber 63490-92-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,9 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63490-92:
(7*6)+(6*3)+(5*4)+(4*9)+(3*0)+(2*9)+(1*2)=136
136 % 10 = 6
So 63490-92-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H23NO6/c1-25-17-6-5-14(20(24)21(17)28-4)9-16-15-11-19(27-3)18(26-2)10-13(15)7-8-22(16)12-23/h5-6,9-12,24H,7-8H2,1-4H3/b16-9-
63490-92-6Relevant academic research and scientific papers
Chemical Transformation of Protoberbines. XI. A Novel Synthesis of 2,3,10,11-Tetraoxygenated Protoberberine Alkaloids from Corresponding 2,3,9,10-Tetraoxygenated Protoberberine Alkaloids.
Hanaoka, Miyoji,Cho, Won Jea,Marutani, Mari,Mukai, Chisato
, p. 195 - 199 (2007/10/02)
2,3,9,10-Tetraoxygenated protoberberin alkaloids, berberine (1a), palmatine (1b), and coptisine (1c) were efficiently converted into the corresponding 12-hydroxy-2,3,10,11-tetraoxygenated protoberberines (6a, 6b, 6c) through an oxidative C8-C8a bond cleav
TRANSFORMATION OF 2,3,9,10-TETRAOXYGENATED PROTOBERBERINE ALKALOIDS INTO 2,3,10,11-TETRAOXYGENATED PROTOBERBERINE ALKALOIDS
Hanaoka, Miyoji,Marutani, Mari,Saitoh, Kazuhiro,Mukai, Chisato
, p. 2927 - 2930 (2007/10/02)
2,3,10,11-Tetraoxygenated tetrahydroprotoberberine (6) were synthesized from the corresponding 2,3,9,10-tetraoxygenated protoberberine alkaloids (1) through oxidative C8-C8a bond cleavage, photocyclization, and deoxygenation.
