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Cbz-N-Methylethylenediamine, also known as CbzNN-C6H10NH2, is an organic compound with the formula C11H17N3O2. It is a derivative of ethylenediamine, characterized by its ability to serve as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals. Cbz-N-Methylethylenediamine is notable for its potential to be further modified to create a variety of functional groups, which enhances its value in the production of complex organic molecules.

19023-94-0

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19023-94-0 Usage

Uses

Used in Pharmaceutical Industry:
Cbz-N-Methylethylenediamine is used as a building block for the synthesis of various pharmaceuticals, leveraging its capacity to be modified into multiple functional groups. This makes it instrumental in the development of a wide array of biologically active compounds, including antifungal agents and antiviral drugs.
Used in Agrochemical Industry:
In the agrochemical sector, Cbz-N-Methylethylenediamine serves a similar role as in pharmaceuticals, acting as a key intermediate in the synthesis of compounds designed to protect crops and enhance agricultural productivity. Its versatility in creating functional groups is crucial for developing new and effective agrochemical products.
Storage and Handling:
Cbz-N-Methylethylenediamine must be handled and stored with care to ensure safety and stability. It should be kept in a dry, well-ventilated area and separated from incompatible materials and sources of ignition to prevent any potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 19023-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,2 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19023-94:
(7*1)+(6*9)+(5*0)+(4*2)+(3*3)+(2*9)+(1*4)=100
100 % 10 = 0
So 19023-94-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N2O2/c1-12-7-8-13-11(14)15-9-10-5-3-2-4-6-10/h2-6,12H,7-9H2,1H3,(H,13,14)

19023-94-0Relevant academic research and scientific papers

Pharmaceutical compositions with attenuated release of phenolic opioids

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Page/Page column 47-48; 51, (2017/01/26)

Pharmaceutical compositions and their methods of use are provided, where the pharmaceutical compositions comprise a phenolic opioid prodrug that provides enzymatically-controlled release of a phenolic opioid, and an enzyme inhibitor that interacts with th

An enzyme and its optional [...] modified ketone and inhibitor composition comprising (by machine translation)

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Paragraph 0364; 0366, (2017/01/23)

PROBLEM TO BE SOLVED: ketone-containing acrylic misuse, abuse or overload is prevented for a new takable amt. provitamin drag pain. SOLUTION: a compound represented by the following formula is represented, in which the drag oxystyrene provitamin hydrocodone ketone-containing acrylic. Pre-selected drug profile is modified and the ketone and schisandrin [...] holding hung contg. compsn. method for administration to a patient. Selected drawing: no (by machine translation)

COMPOSITIONS FOR REDUCING RISK OF ADVERSE EVENTS CAUSED BY DRUG-DRUG INTERACTIONS

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, (2012/09/22)

The present disclosure provides a composition comprising a GABAA agonist and a GI enzyme inhibitor. The present disclosure also provides a composition comprising (a) a GI enzyme inhibitor and (b) a first drug that interacts with a second drug to produce an adverse effect when the second drug is co-ingested as a GI enzyme-cleavable prodrug with the first drug. Such an interaction can be additive or synergistic.

COMPOSITIONS COMPRISING ENZYME-CLEAVABLE PRODRUGS OF ACTIVE AGENTS AND INHIBITORS THEREOF

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, (2011/11/06)

The present disclosure provides pharmaceutical compositions, and their methods of use, where the pharmaceutical compositions comprise a prodrug that provides enzymatically-controlled release of a drug and an enzyme inhibitor that interacts with the enzyme(s) that mediates the enzymatically-controlled release of the drug from the prodrug so as to attenuate enzymatic cleavage of the prodrug. The disclosure provides pharmaceutical compositions which comprise an enzyme inhibitor and a prodrug that contains an enzyme-cleavable moiety that, when cleaved, facilitates release of the drug.

Compositions Comprising Enzyme-Cleavable Phenol-Modified Opioid Prodrugs and Inhibitors Thereof

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, (2011/11/06)

Pharmaceutical compositions and their methods of use are provided, where the pharmaceutical compositions comprise a phenol-modified opioid prodrug that provides enzymatically-controlled release of a phenolic opioid, and an enzyme inhibitor that interacts with the enzyme(s) that mediates the enzymatically-controlled release of the phenolic opioid from the phenol-modified opioid prodrug so as to modify enzymatic cleavage of the phenol-modified opioid prodrug.

Anthrapyrazole anticancer agents. Synthesis and structure-activity relationships against murine leukemias

Showalter,Johnson,Hoftiezer,Turner,Werbel,Leopold,Shillis,Jackson,Elslager

, p. 121 - 131 (2007/10/02)

Chromophore modification of the anthracenediones related to mitoxantrone in an attempt to provide agents with diminished or no cardiotoxicity has resulted in a novel class of DNA binders, the anthrapyrazoles. Their synthesis was carried out by a two-stage

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