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CAS

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791059-05-7

(1S,2R)-2-AMINO-CYCLOOCTANECARBOXYLIC ACID, also known as trans-2-Aminocyclooctanecarboxylic acid, is a chiral cyclic amino acid with the molecular formula C8H15NO2. It features a cyclooctane ring structure and a carboxylic acid functional group, making it a valuable compound in the field of medicinal chemistry and pharmaceuticals.

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  • 791059-05-7 Structure

  • Basic information

    1. Product Name: (1S,2R)-2-AMINO-CYCLOOCTANECARBOXYLIC ACID
    2. Synonyms: (1S,2R)-2-AMINO-CYCLOOCTANECARBOXYLIC ACID
    3. CAS NO:791059-05-7
    4. Molecular Formula: C9H17NO2
    5. Molecular Weight: 171.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 791059-05-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 312.2°C at 760 mmHg
    3. Flash Point: 142.6°C
    4. Appearance: /
    5. Density: 1.058g/cm3
    6. Vapor Pressure: 0.000118mmHg at 25°C
    7. Refractive Index: 1.487
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (1S,2R)-2-AMINO-CYCLOOCTANECARBOXYLIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: (1S,2R)-2-AMINO-CYCLOOCTANECARBOXYLIC ACID(791059-05-7)
    12. EPA Substance Registry System: (1S,2R)-2-AMINO-CYCLOOCTANECARBOXYLIC ACID(791059-05-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 791059-05-7(Hazardous Substances Data)

791059-05-7 Usage

Uses

Used in Pharmaceutical Industry:
(1S,2R)-2-AMINO-CYCLOOCTANECARBOXYLIC ACID is used as a building block for the synthesis of peptidomimetics and other biologically active compounds. Its unique structure and functional groups contribute to the development of new drug molecules with potential therapeutic applications.
Used in Medicinal Chemistry:
(1S,2R)-2-AMINO-CYCLOOCTANECARBOXYLIC ACID is utilized as a key component in the design and creation of innovative drug candidates. Its chiral nature and cyclooctane ring provide a versatile template for the exploration of novel chemical entities with potential therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 791059-05-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,0,5 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 791059-05:
(8*7)+(7*9)+(6*1)+(5*0)+(4*5)+(3*9)+(2*0)+(1*5)=177
177 % 10 = 7
So 791059-05-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO2/c10-8-6-4-2-1-3-5-7(8)9(11)12/h7-8H,1-6,10H2,(H,11,12)/t7-,8+/m0/s1

791059-05-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,2R)-2-aminocyclooctane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names (1S,2R)-2-Amino-cyclooctanecarboxylic acid

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:791059-05-7 SDS

791059-05-7Downstream Products

791059-05-7Relevant articles and documents

Asymmetric synthesis of (1S,2R)-2-aminocyclooctanecarboxylic acid

Garrido, Narciso M.,Blanco, Magda,Cascon, Imanol F.,Diez, David,Vicente, Victor M.,Sanz, Francisca,Urones, Julio G.

experimental part, p. 2895 - 2900 (2009/07/11)

A highly efficient asymmetric synthesis of (1S,2R)-2-aminocyclooctanecarboxylic acid has been completed. This asymmetric synthesis using cycloocta-1,5-diene as the starting material is achieved in 77% yield via a four-step sequence from tert-butyl cycloocta-1,7-dienecarboxylate 10 where the extra double bond adjacent to the unsaturated ester is essential to improve the yield. Furthermore, the Michael adduct intermediate (1S,2R,αR)-14 could be used towards the synthesis of the natural product tashiromine.

Lipase-catalyzed enantioselective ring opening of unactivated alicyclic-fused beta-lactams in an organic solvent.

Forro, Eniko,Fueloep, Ferenc

, p. 1209 - 1212 (2007/10/03)

[reaction: see text] A highly efficient and very simple method was developed for the synthesis of enantiopure beta-amino acids (e.g. cispentacin) and beta-lactams through the enzyme-catalyzed enantioselective ring opening of unactivated alicyclic beta-lac

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