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1-[N-(benzyl)-amino]-2-[N'-(tert-butoxycarbonyl)amino]-1-(indol-3'-yl)ethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

940965-03-7

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940965-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 940965-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,0,9,6 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 940965-03:
(8*9)+(7*4)+(6*0)+(5*9)+(4*6)+(3*5)+(2*0)+(1*3)=187
187 % 10 = 7
So 940965-03-7 is a valid CAS Registry Number.

940965-03-7Downstream Products

940965-03-7Relevant academic research and scientific papers

Total synthesis of marine sponge bis(indole) alkaloids of the topsentin class

Guinchard, Xavier,Vallee, Yannick,Denis, Jean-Noel

, p. 3972 - 3975 (2007)

(Chemical Equation Presented) The synthesis of four natural bis(indole) alkaloids of topsentin class 1 and 2 is described. Their bis(indole) α-carbonylimidazoline and subsequently bis(indole) α- carbonylimidazole moieties have been built via the condensation between indolic α-ketothioimidate salts 4 and l-(indol-3′-y1)-1,2-diaminoethane 3. This compound results from the β-amino indolic hydroxylamine 5 by a two-step sequence. This is the first total synthesis of compounds 1d, 2a, and 2b.

Three-Component Coupling-Oxidative Amidation-Heterocycloannulation: Synthesis of the Indole Alkaloids Hamacanthin A and trans -2,5-Bis(3′-Indolyl)piperazine

Srinivasan, A. Kaliyaperumal,Banerjee, Shyamapada,Pachore, Sharad S.,Syam Kumar

supporting information, p. 1057 - 1064 (2017/05/19)

Concise and highly convergent syntheses of antifungal marine bis(indole) alkaloids, hamacanthin A and trans-2,5-bis(3′-indolyl)piperazine is described. The total synthesis of hamacanthin A is accomplished via the oxidative amidation-chemoselective heterocycloannulation of 2,2-dibromo-1-(1H-indol-3-yl)ethanone with 1-(1H-indol-3-yl)ethane-1,2-diamine. The reduction of desbromo hamacanthin with aluminum borohydride afforded the alkaloid trans-2,5-bis(3′-indolyl)piperazine. Two novel and convenient protocols for the synthesis of indolyl-1,2-diaminoethane are also developed in moderate to good yields.

NOVEL INDOLIC DERIVATIVES, THEIR PREPARATION PROCESSES AND THEIR USES IN PARTICULAR AS ANTIBACTERIALS

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Page/Page column 35-36, (2010/06/19)

The invention relates to the use of at least one compound of the formula (I), in which R and R3 are particularly a hydrogen atom, R1 is particularly a hydrogen atom or a methyl, ethyl or isobutyl mi group, R4, R5, R6 and R7 are independently a hydrogen atony, an alkoxyl group with 1 to 7 carbon atoms or a halogen atom, R2 is a hydrogen atom, an O? group or an OH group, B is an N-GP1 or NRc, group, GP1 being a Boc or Cbz group, and Rc is a hydrogen atom or a methyl or t-butyl group, for preparing a drug for treating conditions associated with bacterial infections, in particular for treating bacterial diseases.

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