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Methyl cis-3-(Boc-amino)cyclohexane carboxylate is a chemical compound categorized as an amino acid derivative. It is characterized by a molecular formula of C13H23NO4 and a molecular weight of 257.33 g/mol. The name "methyl cis-3-(Boc-amino)cyclohexane carboxylate" reflects its structural components, which include a methyl group, a Boc-protected amino group, and a cyclohexane carboxylate moiety. Methyl cis-3-(Boc-aMino)c... is recognized for its utility in peptide synthesis and organic chemistry research, with its well-defined structure and functional groups being instrumental in the creation of pharmaceuticals and other biologically active molecules.

142733-63-9

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142733-63-9 Usage

Uses

Used in Pharmaceutical Development:
Methyl cis-3-(Boc-amino)cyclohexane carboxylate is utilized as a building block in the synthesis of complex pharmaceuticals. Its Boc-protected amino group and cyclohexane carboxylate moiety contribute to the structural diversity and functional properties of the resulting drug molecules, enhancing their therapeutic potential.
Used in Peptide Synthesis:
In the field of peptide synthesis, Methyl cis-3-(Boc-amino)cyclohexane carboxylate serves as a key intermediate. Its incorporation allows for the creation of peptides with specific biological activities, such as enzyme inhibitors or receptor agonists/antagonists, which are crucial for various therapeutic applications.
Used in Organic Chemistry Research:
Methyl cis-3-(Boc-amino)cyclohexane carboxylate is employed as a versatile reagent in organic chemistry research. Its unique structure facilitates the exploration of novel synthetic pathways and the development of innovative chemical reactions, broadening the scope of organic synthesis.
Used in the Synthesis of Biologically Active Molecules:
Methyl cis-3-(Boc-amino)cyclohexane carboxylate is used as a precursor in the synthesis of biologically active molecules. Its functional groups enable the attachment of various moieties, leading to the creation of compounds with potential applications in medicine, agriculture, and other fields.

Check Digit Verification of cas no

The CAS Registry Mumber 142733-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,7,3 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 142733-63:
(8*1)+(7*4)+(6*2)+(5*7)+(4*3)+(3*3)+(2*6)+(1*3)=119
119 % 10 = 9
So 142733-63-9 is a valid CAS Registry Number.

142733-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl cis-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)cyclobuta necarboxylate

1.2 Other means of identification

Product number -
Other names (1s,3s)-methyl 3-((tert-butoxycarbonyl)amino)cyclobutanecarboxylate

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:142733-63-9 SDS

142733-63-9Relevant academic research and scientific papers

SYNTHESIS OF NEW CARBOCYCLIC ANALOGUES OF OXETANOCIN A AND OXETANOCIN G

Pecquet, Pascal,Huet, Francois,Legraverend, Michel,Bisagni, Emile

, p. 739 - 745 (2007/10/02)

The synthesis of cis-3-amino-1-cyclobutanemethanol has been performed in six steps (59.6percent yield) from cis-1,3-cyclobutanedicarboxylic anhydride.This allowed us to obtain two new carbocyclic analogues of oxetanocin A and oxetanocin G related to 7-deazaadenosine and 7-deazaguanosine.

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