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853056-96-9

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853056-96-9 Usage

Description

(R)-N-METHOXY-N-METHYL-1-((S)-1-PHENYLETHYL)AZIRIDINE-2-CARBOXAMIDE, also known as Enamine, is a chemical compound characterized by its 1,2-aziridine monocyclic ring. It is an organic or inorganic compound with significant potential in the synthesis of various compounds with organoleptic properties, such as aroma compounds and fragrances. Its unique chemical structure also positions it as a promising candidate for pharmaceutical applications, particularly in the development of antineoplastic agents for tumor treatment.

Uses

Used in Aroma Compounds and Fragrances:
(R)-N-METHOXY-N-METHYL-1-((S)-1-PHENYLETHYL)AZIRIDINE-2-CARBOXAMIDE is used as a synthetic building block for creating aroma compounds and fragrances. Its organoleptic properties make it a valuable component in the development of scents and flavors for various industries, including cosmetics, food, and beverages.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (R)-N-METHOXY-N-METHYL-1-((S)-1-PHENYLETHYL)AZIRIDINE-2-CARBOXAMIDE is used as a starting material for the development of pharmaceutical products. Its unique chemical structure allows for the creation of new compounds with potential therapeutic applications.
Used as an Antineoplastic Agent:
(R)-N-METHOXY-N-METHYL-1-((S)-1-PHENYLETHYL)AZIRIDINE-2-CARBOXAMIDE is used as an antineoplastic agent for the treatment of tumors. Its potential therapeutic uses make it a promising candidate for further research and development in oncology, with the aim of improving cancer treatment options and patient outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 853056-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,0,5 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 853056-96:
(8*8)+(7*5)+(6*3)+(5*0)+(4*5)+(3*6)+(2*9)+(1*6)=179
179 % 10 = 9
So 853056-96-9 is a valid CAS Registry Number.

853056-96-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-N-METHOXY-N-METHYL-1-((S)-1-PHENYLETHYL)AZIRIDINE-2-CARBOXAMIDE

1.2 Other means of identification

Product number -
Other names L-N-isopropylvalinol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:853056-96-9 SDS

853056-96-9Relevant articles and documents

Structure and conserved function of iso-branched sphingoid bases from the nematode: Caenorhabditis elegans

Thomas Hannich,Mellal, Denia,Feng, Suihan,Zumbuehl, Andreas,Riezman, Howard

, p. 3676 - 3686 (2017/07/10)

Sphingolipids are bio-active metabolites that show structural diversity among eukaryotes. They are essential for growth of all eukaryotic cells but when produced in an uncontrolled manner can lead to cell death and pathologies including auto-immune reacti

3,4-Disubstituted oxazolidin-2-ones as constrained ceramide analogs with anticancer activities

Singh, Alok,Ha, Hyun-Joon,Park, Jungchan,Kim, Jun Hee,Lee, Won Koo

scheme or table, p. 6174 - 6181 (2011/12/02)

Heterocyclic analogs of ceramide as 3-alkanoyl or benzoyl-4-(1-hydroxy-2- enyl)-oxazolidin-2-ones were designed by binding of primary alcohol and amide in sphinogosine backbone as a carbamate. They were synthesized by addition of acyl halide to the common

Synthesis of constrained ceramide analogs and their potent antileukemic activities

Ha, Hyun-Joon,Hong, Myeng Chan,Ko, Seung Whan,Kim, Yong Woo,Lee, Won Koo,Park, Jungchan

, p. 1880 - 1883 (2007/10/03)

Constrained ceramide analogs were designed and synthesized by binding terminal alcohol and amine of ceramide with additional carbonyl functional group as 3-acetyl (3), 3-propionyl (4), 3-benzoyl (5), and 3-hexadecanoyl-4-(1- hydroxyhexadec-2-enyl)-oxazoli

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