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(4aS,4bR,6aS,8S,10aS,10bS,12aS)-10a,12a-dimethyl-2-oxooctadecahydronaphtho[2,1-f]quinolin-8-yl 4-[bis(2-chloroethyl)amino]phenylacetate is a complex organic molecule characterized by a quinoline core structure and a chloroethylamine side chain. (4aS,4bR,6aS,8S,10aS,10bS,12aS)-10a,12a-dimethyl-2-oxooctadecahydronaphtho[2,1-f]quinolin-8-yl 4-[bis(2-chloroethyl)amino]phenylacetate's unique stereochemistry and functional groups, including an acyl and an aromatic ester, suggest potential for enzymatic hydrolysis and a range of biological activities. This makes it a promising candidate for various applications, particularly as a therapeutic agent or chemical probe.

43000-65-3

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43000-65-3 Usage

Uses

Used in Pharmaceutical Industry:
(4aS,4bR,6aS,8S,10aS,10bS,12aS)-10a,12a-dimethyl-2-oxooctadecahydronaphtho[2,1-f]quinolin-8-yl 4-[bis(2-chloroethyl)amino]phenylacetate is used as a potential therapeutic agent for its possible bioactivity and reactivity due to the presence of the chloroethylamine side chain. (4aS,4bR,6aS,8S,10aS,10bS,12aS)-10a,12a-dimethyl-2-oxooctadecahydronaphtho[2,1-f]quinolin-8-yl 4-[bis(2-chloroethyl)amino]phenylacetate's structural features and functional groups may allow for interactions with biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (4aS,4bR,6aS,8S,10aS,10bS,12aS)-10a,12a-dimethyl-2-oxooctadecahydronaphtho[2,1-f]quinolin-8-yl 4-[bis(2-chloroethyl)amino]phenylacetate serves as a valuable chemical probe. Its unique structure and functional groups can be utilized to study various biological processes and interactions, contributing to a deeper understanding of molecular mechanisms and the development of novel chemical strategies.
Used in Drug Delivery Systems:
(4aS,4bR,6aS,8S,10aS,10bS,12aS)-10a,12a-dimethyl-2-oxooctadecahydronaphtho[2,1-f]quinolin-8-yl 4-[bis(2-chloroethyl)amino]phenylacetate may also be employed in the development of drug delivery systems. (4aS,4bR,6aS,8S,10aS,10bS,12aS)-10a,12a-dimethyl-2-oxooctadecahydronaphtho[2,1-f]quinolin-8-yl 4-[bis(2-chloroethyl)amino]phenylacetate's potential for enzymatic hydrolysis could be harnessed to design targeted drug release mechanisms, improving the efficacy and bioavailability of therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 43000-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,0,0 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 43000-65:
(7*4)+(6*3)+(5*0)+(4*0)+(3*0)+(2*6)+(1*5)=63
63 % 10 = 3
So 43000-65-3 is a valid CAS Registry Number.

43000-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [(4aS,4bR,6aS,8S,10aS,10bS,12aS)-10a,12a-dimethyl-2-oxo-3,4,4a,4b,5,6,6a,7,8,9,10,10b,11,12-tetradecahydro-1H-naphtho[2,1-f]quinolin-8-yl] 2-[4-[bis(2-chloroethyl)amino]phenyl]acetate

1.2 Other means of identification

Product number -
Other names DAL-8

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:43000-65-3 SDS

43000-65-3Downstream Products

43000-65-3Relevant academic research and scientific papers

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