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63490-92-6

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63490-92-6 Usage

Description

(Z)-3,4-Dihydro-1-(2-hydroxy-3,4-dimethoxybenzylidene)-6,7-dimethoxyisoquinoline-2(1H)-carbaldehyde is a complex organic compound belonging to the benzylisoquinoline alkaloid family. It is derived from the plant Enantia polycarpa and can be crystallized to form colorless rods when dissolved in methanol (MeOH). (Z)-3,4-Dihydro-1-(2-hydroxy-3,4-dimethoxybenzylidene)-6,7-dimethoxyisoquinoline-2(1H)-carbaldehyde exhibits unique optical properties, as demonstrated by its ultraviolet spectrum in ethanol (EtOH) with absorption maxima at 222 and 332 nm, accompanied by a shoulder at 262 nm.

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-

63490-92-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1Z)-1-[(2-hydroxy-3,4-dimethoxyphenyl)methylidene]-6,7-dimethoxy-3,4-dihydroisoquinoline-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names polycarpine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:63490-92-6 SDS

63490-92-6Relevant articles and documents

-

Murugesan,Shamma

, p. 4521,4522 (1979)

-

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.

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