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2-benzyloxy-5,6,12,12a-tetrahydro-3,9,10-trimethoxydibenz[b,g]indolizine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17138-39-5

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17138-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17138-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,3 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17138-39:
(7*1)+(6*7)+(5*1)+(4*3)+(3*8)+(2*3)+(1*9)=105
105 % 10 = 5
So 17138-39-5 is a valid CAS Registry Number.

17138-39-5Relevant academic research and scientific papers

N-fused indolines through non-carbonyl-stabilized rhodium carbenoid C-H insertion of N-aziridinyl imines

Mahoney, Stuart J.,Fillion, Eric

, p. 68 - 71 (2012/02/04)

Under rhodium catalysis, N-aziridinyl imines provided access to N-fused indolines through non-carbonyl-stabilized rhodium carbenoid C-H insertion. The utility of this methodology for the synthesis of architecturally complex heterocycles was further demonstrated by an expedient total synthesis of ( ±)-cryptaustoline (see scheme). Copyright

Use of (NHC)Pd(η3-allyl)Cl (NHC = N-Heterocyclic Carbene) in a Palladium-mediated Approach to Cryptocarya Alkaloids

C?mmerer, Simon S.,Viciu, Mihai S.,Stevens, Edwin D.,Nolan, Steven P.

, p. 1871 - 1873 (2007/10/03)

The palladium-mediated intramolecular aryl amination of 7-benzyloxy-1-(2-bromo-4,5-dimethoxy-benzyl)-1,2,3, 4-tetrahydro-6-methoxy-isoquinoline catalyzed by a recently discovered, air and moisture stable (NHC)Pd(η3-allyl)Cl (NHC = N-heterocycli

A facile route to indolo[2,1-a]isoquinolines and dibenzopyrrocoline alkaloids

Orito, Kazuhiko,Harada, Rika,Uchiito, Shiho,Tokuda, Masao

, p. 1799 - 1801 (2007/10/03)

(Formula presented) Treatment of 1-(2′-bromobenzyl)-3,4-dihydroisoquinolines 2 in the presence of K2CO3 in boiling DMF efficiently provided a variety of alkoxysubstituted indolo[2,1-a]isoquinolines 3. Application of this cyclization

A NOVEL TOTAL SYNTHESIS OF (+/-)-CRYPTAUSTOLINE, A DIBENZOPYRROCOLINE ALKALOID

Yasuda, Shingo,Hirasawa, Taeko,Yoshida, Shuji,Hanaoka, Miyoji

, p. 1682 - 1683 (2007/10/02)

(+/-)-Cryptaustoline (1), a dibenzopyrrocoline alkaloid, was efficiently synthesized from the readily available N-phenethylaniline (7) via the N-phenethyloxindole (12) or the N-phenethylindole (14) by the Bischler-Napieralski reaction or by radical cycliz

SILICON-MEDIATED ISOQUINOLINE ALKALOID SYNTHESIS: A NEW ROUTE TO THE DIBENZOPYRROCOLINE ALKALOID (+/-)-CRYPTAUSTOLINE

Takano, Seiichi,Satoh, Shigeki,Ogasawara, Kunio

, p. 1483 - 1485 (2007/10/02)

A fundamentally new synthesis of the benzopyrrocoline alkaloid (+/-)-cryptaustoline iodide (12) has been devised by employing the silicon mediated ring closure through a formal 5-Endo-Trigonal process.

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