70866-38-5 Usage
Uses
Used in Medicinal Chemistry:
2,3-dimethoxy-6-[(6-methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl)methyl]phenylmethanol is used as a key intermediate for the synthesis of various pharmaceutical compounds due to its complex structure and potential reactivity.
Used in Organic Synthesis:
In the field of organic synthesis, 2,3-dimethoxy-6-[(6-methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl)methyl]phenylmethanol serves as a valuable building block for creating novel molecules with potential applications in various industries.
Used in Pharmacological Research:
2,3-dimethoxy-6-[(6-methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl)methyl]phenylmethanol is used as a research tool to study its potential effects on neurotransmission and neuronal function, given the presence of the tetrahydroisoquinoline ring.
Used in the Pharmaceutical Industry:
In the pharmaceutical industry, 2,3-dimethoxy-6-[(6-methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl)methyl]phenylmethanol is used as a starting material for the development of new drugs targeting neurological disorders and other conditions related to neurotransmission.
Used in the Chemical Industry:
2,3-dimethoxy-6-[(6-methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl)methyl]phenylmethanol is utilized in the chemical industry for the production of specialty chemicals and materials that can be applied in various sectors, such as coatings, adhesives, and polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 70866-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,8,6 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70866-38:
(7*7)+(6*0)+(5*8)+(4*6)+(3*6)+(2*3)+(1*8)=145
145 % 10 = 5
So 70866-38-5 is a valid CAS Registry Number.
70866-38-5Relevant academic research and scientific papers
Pyrolysis and Photolysis of the N-Oxides of Protopines and Hexahydrobenzophenanthridines. Syntheses of the Secoberbines and Benzophenanthridines
Iwasa, Kinuko,Sugiura, Makiko,Takao, Narao
, p. 998 - 1008 (2007/10/02)
Pyrolysis and photolysis of the N-oxides of the protopines 9 and 16 produces the ring-enlarged compounds 10 and 17, whose reduction with zinc in acetic acid leads to the secoberbines (+/-)-corydalisol (11) and (+/-)-hypecorine (12) from 9, and the corresponding analogs (18 and 19) from 16.Pyrolysis of (+)-chelidonine N-oxide (24) generates dihydrosanguinarine (22).Keywords - pyrolysis; photolysis; N-oxide; protopine; sanguinarine; corydalisol; hypecorine
Chemical Transformation of Protoberberines. IV. A Novel, Simple Synthesis of (+/-)-Canadaline and a Retroprotoberberine from Tetrahydroberberine
Hanaoka, Miyoji,Nagami, Kazuyoshi,Inoue, Mitsuru,Yasuda, Shingo
, p. 2685 - 2690 (2007/10/02)
Heating of tetrahydroberberine (1) in ethyl chloroformate preferentially afforded the C8-N bond cleavage (4) with small amounts of the C6-N and C14-N bond cleavage products (5 and 6, respectively).The urethane (4) was effe
THE PYROLYSIS AND PHOTOLYSIS OF THE PROTOPINE TYPE ALKALOID N-OXIDES. THE SYNTHESIS OF THE SECOBERBINES AND BENZOPHENANTHRIDINES
Iwasa, Kinuko,Takao, Narao
, p. 1535 - 1539 (2007/10/02)
The pyrolysis of the N-oxides of the protopine-type alkaloids afforded three products, one of which was converted to the naturally occurring secoberbines.The photolysis of the N-oxides of the protopines supplied the benzophenanthridines as well as the one of the pyrolysis products.
