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1385-43-9

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1385-43-9 Usage

General Description

2,3,5,6-tetramethoxy-9,11,12,13,13a,14-hexahydrodibenzo[f,h]pyrrolo[1,2-b]isoquinoline is a chemical compound with a complex structure that contains multiple methoxy (CH3O) groups and a dibenzo[f,h]pyrrolo[1,2-b]isoquinoline core. 2,3,5,6-tetramethoxy-9,11,12,13,13a,14-hexahydrodibenzo[f,h]pyrrolo[1,2-b]isoquinoline is a type of alkaloid and is not commonly found in nature, but can be synthesized in a laboratory. It may have potential pharmacological properties due to its unique structure and could be of interest for medicinal or research purposes. However, further studies and research are needed to understand its potential uses and effects on the human body.

Check Digit Verification of cas no

The CAS Registry Mumber 1385-43-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,3,8 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1385-43:
(6*1)+(5*3)+(4*8)+(3*5)+(2*4)+(1*3)=79
79 % 10 = 9
So 1385-43-9 is a valid CAS Registry Number.

1385-43-9Downstream Products

1385-43-9Relevant articles and documents

Total synthesis of (S)-(+)-tylophorine via enantioselective intramolecular alkene carboamination

Zeng, Wei,Chemler, Sherry R.

, p. 6045 - 6047 (2008)

(Chemical Equation Presented) The enantioselective synthesis of (S)-(+)-tylophorine, a potent cancer cell growth inhibitor, has been accomplished in eight steps from commercially available 3,4-dimethoxybenzyl alcohol. A copper (II)-catalyzed enantioselective intramolecular alkene carboanimation was employed as the key step to construct the chiral indolizidine ring.

Collective asymmetric synthesis of (-)-Antofine, (-)-cryptopleurine, (-)-tylophorine, and (-)-tylocrebrine with tert- butanesulfinamide as a chiral auxiliary

Zheng, Yanlong,Liu, Yuxiu,Wang, Qingmin

, p. 3348 - 3357 (2014/05/06)

A collective asymmetric synthesis of phenanthroindolizidine and phenanthroquinolizidine alkaloids (-)-antofine, (-)-cryptopleurine, (-)-tylophorine, and (-)-tylocrebrine was achieved by means of a reaction sequence involving efficient generation of chiral homoallylic amine intermediates by asymmetric allylation of the corresponding tert-butanesulfinyl imine. From these intermediates, the pyrrolidine and piperidine rings were constructed by means of an intramolecular SN2 substitution reaction and a ring-closing metathesis reaction, respectively. The unusual C5-methoxy-substituted phenanthrene moiety of (-)-tylocrebrine was generated by means of an InCl3-catalyzed cycloisomerization reaction of an o-propargylbiaryl compound.

Compounds and compositions for treating infection

-

, (2009/04/24)

Compounds from 14 Kenyan plants, including from the root of Dovyalis abyssinica and Clutia robusta have been characterized and isolated, and their uses are disclosed.

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