19485-63-3 Usage
Description
1,2,3,4-Tetrahydro-6-methoxy-2-methyl-1-(2-methylpropyl)isoquinolin-7-ol is an alkaloid belonging to the isoquinoline group. It is one of the cactus bases found in Lophocereus schottii and is characterized as a colorless oil. 1,2,3,4-Tetrahydro-6-methoxy-2-methyl-1-(2-methylpropyl)isoquinolin-7-ol has a crystalline picrate and a styphnate with melting points of 191.5-193°C and 171-2°C, respectively. Its structure has been confirmed, and it can yield a methyl ether, which also forms a picrate and a styphnate with melting points of 180-2°C and 210-2°C, respectively. The corresponding ethyl ether of this compound also gives a picrate and styphnate with melting points of ISO-3°C and 182-3°C.
Uses
1. Used in Pharmaceutical Industry:
1,2,3,4-Tetrahydro-6-methoxy-2-methyl-1-(2-methylpropyl)isoquinolin-7-ol is used as a pharmaceutical compound for its potential therapeutic applications. As an alkaloid from the isoquinoline group, it may possess bioactive properties that can be harnessed for the development of new drugs or treatments.
2. Used in Chemical Research:
1,2,3,4-Tetrahydro-6-methoxy-2-methyl-1-(2-methylpropyl)isoquinolin-7-ol is used as a subject of study in chemical research, particularly in the field of natural products and their derivatives. Its unique structure and properties make it an interesting candidate for further investigation, which could lead to the discovery of new applications or insights into its chemical behavior.
3. Used in Analytical Chemistry:
The various derivatives of 1,2,3,4-Tetrahydro-6-methoxy-2-methyl-1-(2-methylpropyl)isoquinolin-7-ol, such as its methyl ether and ethyl ether, can be used in analytical chemistry for the development of new methods or techniques for compound identification and analysis. Their distinct melting points and reactivity with other compounds make them valuable tools in this field.
4. Used in Material Science:
The crystalline properties of the picrate and styphnate derivatives of this compound may have potential applications in material science, particularly in the development of new materials with unique properties or for use in specific applications where their specific characteristics can be advantageous.
Synthesis Reference(s)
The Journal of Organic Chemistry, 24, p. 1106, 1959 DOI: 10.1021/jo01090a018
References
Bobbitt, Chou., J. Org. Chem., 24, 1106 (1959)
Check Digit Verification of cas no
The CAS Registry Mumber 19485-63-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,8 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19485-63:
(7*1)+(6*9)+(5*4)+(4*8)+(3*5)+(2*6)+(1*3)=143
143 % 10 = 3
So 19485-63-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H23NO2/c1-10(2)7-13-12-9-14(17)15(18-4)8-11(12)5-6-16(13)3/h8-10,13,17H,5-7H2,1-4H3
19485-63-3Relevant articles and documents
A novel reductive amino-cyclization method and its application for the total syntheses of (±)-aurantio-clavine and (±)-lophocerine
Somei, Masanori,Yamada, Fumio
, p. 943 - 950 (2008/09/19)
A novel reductive amino-cyclization method for the synthesis of azacycloalkanes is developed. Its versatility is proved by the total syntheses of (±)-aurantioclavine (1), an ergot alkaloid, and (±)-lophocerine (2), a cactus alkaloid, as examples of azepan
