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Benzaldehyde, 6-bromo-2-methoxy-3-(phenylmethoxy)-, also known as 6-bromo-2-methoxy-3-(phenylmethoxy)benzaldehyde, is an organic compound with the molecular formula C15H13BrO3. It is a derivative of benzaldehyde, featuring a bromine atom at the 6th position, a methoxy group at the 2nd position, and a phenylmethoxy group at the 3rd position. Benzaldehyde, 6-bromo-2-methoxy-3-(phenylmethoxy)- is characterized by its aromatic structure and the presence of functional groups that contribute to its chemical properties. It is used in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique structure and reactivity.

95712-55-3

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95712-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95712-55-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,7,1 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95712-55:
(7*9)+(6*5)+(5*7)+(4*1)+(3*2)+(2*5)+(1*5)=153
153 % 10 = 3
So 95712-55-3 is a valid CAS Registry Number.

95712-55-3Relevant academic research and scientific papers

Synthesis of 1,7-dimethoxy-2-hydroxyxanthone, a natural product with potential activity on erectile dysfunction

Liu, Wen-Jing,Mei, De-Sheng,Duan, Wen-Hu

, p. 515 - 517 (2013/07/27)

The natural product, 1,7-dimethoxy-2-hydroxyxanthone (1), isolated from Securidaca inappendiculate Hassk, has a potential in the treatment of erectile dysfunction due to its significant relaxation activity on rabbit Corpus cavernosum. However, the isolation of compound 1 is problematic because of its high similarity in structure to its analogs. In this paper, the first synthesis of 1 was reported featuring two key reactions: a copper-catalyzed coupling reaction and an intramolecular cyclization.

Revision of the structure of fagaridine based on the comparison of UV and NMR data of synthetic compounds

Nakanishi, Takeshi,Suzuki, Masanobu

, p. 1263 - 1267 (2007/10/03)

Fagaridine is a quaternary benzo[c]phenanthridine alkaloid, originally isolated from Fagara xanthoxyloides in 1973. The assigned structure of this alkaloid was 7-hydroxy-8-methoxy-5-methyl-2,3-(methylenedioxy)- benzo[c]phenanthridinium (1). We have synthe

Benzyne Cyclization Route to Benzophenanthridine Alkaloids. Synthesis of Chelerythrine, Decarine, and Nitidine

Kessar, Satinder V.,Gupta, Yash P.,Balakrishnan, Prasanna,Sawal, Kewal K.,Mohammad, Taj,Dutt, Mahesh

, p. 1708 - 1713 (2007/10/02)

The alkaloids chelerythrine (8b) and decarine (7c) have been synthesized through a benzyne-mediated cyclization of N-(2-halobenzyl)-1-naphthylamines 4 with KNH2 in ammonia/ether.The 7-hydroxybenzophenanthridine structure 16a proposed for the alkaloid fagaridine is questioned on the basis of comparison with a model compound (16b) synthesized by benzyne cyclization.For the 8,9-oxygenated alkaloids like nitidine (8i), this cyclization proceeded poorly, but a dramatic improvement occurred when LDA/THF at -78 deg C was used instead of KNH2/NH3.

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