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3-Piperidinecarboxylic acid, 1-[N-[(1,1-dimethylethoxy)carbonyl]-2-methylalanyl-D-tryptophyl]-3-(phenylmethyl)-, trimethylhydrazide, (3R)is a complex organic compound that is a derivative of piperidinecarboxylic acid. It features a 1-[N-[(1,1-dimethylethoxy)carbonyl]-2-methylalanyl-D-tryptophyl]-3-(phenylmethyl)group and has a 3R stereochemistry. 3-Piperidinecarboxylic acid,
1-[N-[(1,1-dimethylethoxy)carbonyl]-2-methylalanyl-D-tryptophyl]-3-(phen
ylmethyl)-, trimethylhydrazide, (3R)may have potential applications in pharmaceutical research and development, either as a drug candidate or as a tool compound for studying biological processes. Further research is necessary to fully understand its properties and potential uses.

339539-90-1

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339539-90-1 Usage

Uses

Used in Pharmaceutical Research and Development:
3-Piperidinecarboxylic acid, 1-[N-[(1,1-dimethylethoxy)carbonyl]-2-methylalanyl-D-tryptophyl]-3-(phenylmethyl)-, trimethylhydrazide, (3R)is used as a potential drug candidate for the development of new medications. Its unique structure and properties may offer novel therapeutic opportunities in various medical fields.
Used in Biological Research:
3-Piperidinecarboxylic acid, 1-[N-[(1,1-dimethylethoxy)carbonyl]-2-methylalanyl-D-tryptophyl]-3-(phenylmethyl)-, trimethylhydrazide, (3R)is used as a tool compound in biological research to study various biological processes. Its complex structure allows researchers to investigate its interactions with biological targets and understand its potential effects on cellular and molecular mechanisms.

Check Digit Verification of cas no

The CAS Registry Mumber 339539-90-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,9,5,3 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 339539-90:
(8*3)+(7*3)+(6*9)+(5*5)+(4*3)+(3*9)+(2*9)+(1*0)=181
181 % 10 = 1
So 339539-90-1 is a valid CAS Registry Number.

339539-90-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (R,R)-{1-[2-[3-benzyl-3-(N,N',N'-trimethyl-hydrazinocarbonyl)piperidin-1-yl]-1-(1H-indol-3-ylmethyl)-2-oxo-ethylcarbamoyl]-1-methylethyl}carbamic acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names {1-[(1R)-2-[(3R)-3-benzyl-3-(N,N'',N''-trimethylhydrazincarbonyl)piperidin-1-yl-]-1-(1H-indol-3-ylmethyl)-2-oxo-ethylcarbamoyl]-1-methylethyl}carbamic acid tert-butyl ester

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:339539-90-1 SDS

339539-90-1Relevant academic research and scientific papers

A practical synthesis of the pseudotripeptide RC-1291

Paul, Bernhard J.,Littler, Benjamin J.,Jos, Frederic,Vogt, Paul F.,Pines, Seemon H.

, p. 339 - 345 (2012/12/22)

The rapid process development of a scaleable synthesis of the pseudotripeptide RC-1291 for preclinical and clinical evaluation is described. By employing a nontraditional N-to-C coupling strategy, the peptide chain of RC-1291 was assembled in high yield, with minimal racemization and in an economical manner by introducing the most expensive component last. A one-pot deprotection/crystallization procedure was developed for the isolation of RC-1291 free base, which afforded the target compound in excellent yield and with a purity of >99.5% without chromatographic purification.

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