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1H-Indene-3-carbonitrile, 2-amino-3a,4,5,6,7,7a-hexahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

959009-59-7

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959009-59-7 Usage

General Description

1H-Indene-3-carbonitrile, 2-amino-3a,4,5,6,7,7a-hexahydro- is a chemical compound with the formula C11H14N2. It is a heterocyclic compound containing a nitrile group and an amino group. The compound has a cyclic structure with six-membered and five-membered rings, and the amino group is attached to the six-membered ring. 1H-Indene-3-carbonitrile, 2-amino-3a,4,5,6,7,7a-hexahydro- has potential applications in the pharmaceutical and chemical industries due to its unique structure and properties. Further research and development may reveal additional uses and potential benefits of 1H-Indene-3-carbonitrile, 2-amino-3a,4,5,6,7,7a-hexahydro-.

Check Digit Verification of cas no

The CAS Registry Mumber 959009-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,9,0,0 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 959009-59:
(8*9)+(7*5)+(6*9)+(5*0)+(4*0)+(3*9)+(2*5)+(1*9)=207
207 % 10 = 7
So 959009-59-7 is a valid CAS Registry Number.

959009-59-7Downstream Products

959009-59-7Relevant academic research and scientific papers

Struktur eines O,N-Ketenacetals: (1RS,8SR,10SR)4(15)Z)-4-Aethyliden-5-oxa-3-azatricyclo3,8>tetradecan)

Kuemin, Albin,Maverick, Emily,Seiler, Paul,Vanier, Noel,Damm, Lorenz,et al.

, p. 1158 - 1175 (2007/10/02)

Methods for the preparation of a series of model compounds which were required for stereochemical studies are described: the tricyclic O,N-ketenacetal 1, the two diastereomeric bicyclic amino acids 7 and 10 (see Scheme 2), and the two diastereomeric conformationally fixed tetrahydro-1,3-oxazines (=1,3-oxazines) 9 and 11.An x-ray analysis of racemic 1 reveals a quasi-tetrahedral nitrogen pyramid of the O,N-ketene acetal grouping, and an almost perfect conformational analogy between the N- and C-centered allylic positions at the double bond.

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