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(1E)-3-aminopropanimidamide, an imidamide derivative with the molecular formula C4H11N3, is an organic base that likely exhibits basic properties. Its structure features a 3-aminopropanimidamide functional group, which may contribute to its potential applications in chemical and pharmaceutical processes. As a building block, it could be utilized in the synthesis of other organic compounds, although the exact uses and properties may vary depending on the specific application and manufacturing process.

77152-88-6

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77152-88-6 Usage

Uses

Used in Chemical Synthesis:
(1E)-3-aminopropanimidamide is used as a building block for the synthesis of other organic compounds, leveraging its imidamide derivative structure for creating a variety of chemical products.
Used in Pharmaceutical Processes:
(1E)-3-aminopropanimidamide is used as an intermediate in pharmaceutical processes, potentially contributing to the development of new drugs or improving the synthesis of existing ones due to its basic properties and functional group.

Check Digit Verification of cas no

The CAS Registry Mumber 77152-88-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,5 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77152-88:
(7*7)+(6*7)+(5*1)+(4*5)+(3*2)+(2*8)+(1*8)=146
146 % 10 = 6
So 77152-88-6 is a valid CAS Registry Number.

77152-88-6Relevant academic research and scientific papers

Asymmetric total synthesis of sperabillins B and D via lithium amide conjugate addition

Davies, Stephen G.,Haggitt, Jane R.,Ichihara, Osamu,Kelly, Richard J.,Leech, Michael A.,Mortimer, Anne J. Price,Roberts, Paul M.,Smith, Andrew D.

, p. 2630 - 2649 (2007/10/03)

Diastereoselective conjugate addition of homochiral lithium (R)-N-allyl-N-α-methylbenzylamide to methyl (2E,5E)-hepatadienoate, followed by protecting group manipulation and subsequent iodocyclocarbamation allows a concise route to the core fragment, methyl (3R,5R,6R)-3,6-diamino-5- hydroxyheptanoate, of sperabillins B and D. Differentiation between the C-3 and C-6 primary amino groups of this core amino acid was readily achieved by treatment with acetone, giving the 5,6-isopropylidene and C-3-imine protected diamine, with subsequent regioselective acylation of the C-6-nitrogen facilitating the total synthesis of sperabillin D in 10.8% overall yield, and the first asymmetric synthesis of sperabillin B in 5.8% overall yield.

DEPSIPEPTIDE ANALOGS OF THE ANTITUMOR DROG DISTAMYCIN CONTAINING THIAZOLE AMINO ACIDS RESIDUES

Bailly, Christian,Houssin, Raymond,Bernier, Jean-Luc,Henichart, Jean-Pierre

, p. 5833 - 5844 (2007/10/02)

Three compounds structurally related to the natural antiviral antitumor drugs netropsin and distamycin have been synthetized.They have been designed starting from 2-(aminomethyl)-thiazole-4 carboxylic acid, gly (Thz), a key element in the structure of hig

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