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(R)-2-(TERT-BUTOXYCARBONYLAMINO)-2-((1R,4R)-4-HYDROXYCYCLOHEXYL)ACETIC ACID is a specific enantiomer of a cyclohexylacetic acid derivative featuring a tert-butoxycarbonylamino group and a hydroxycyclohexylacetic acid group. The (R) configuration denotes a unique three-dimensional arrangement of atoms, which is crucial for its biological activity and pharmacological properties. (R)-2-(TERT-BUTOXYCARBONYLAMINO)-2-((1R,4R)-4-HYDROXYCYCLOHEXYL)ACETIC ACID is commonly utilized in the synthesis of pharmaceuticals and biologically active compounds, and it may have potential applications in medicinal chemistry and drug development.

130624-89-4

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130624-89-4 Usage

Uses

Used in Pharmaceutical Synthesis:
(R)-2-(TERT-BUTOXYCARBONYLAMINO)-2-((1R,4R)-4-HYDROXYCYCLOHEXYL)ACETIC ACID is used as a key intermediate in the synthesis of pharmaceuticals for its unique stereochemistry and reactivity, contributing to the development of new drugs with improved efficacy and selectivity.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (R)-2-(TERT-BUTOXYCARBONYLAMINO)-2-((1R,4R)-4-HYDROXYCYCLOHEXYL)ACETIC ACID serves as a valuable research tool for studying the structure-activity relationships of biologically active molecules. Its specific configuration allows for the exploration of the impact of stereochemistry on drug-target interactions and pharmacokinetics.
Used in Drug Development:
(R)-2-(TERT-BUTOXYCARBONYLAMINO)-2-((1R,4R)-4-HYDROXYCYCLOHEXYL)ACETIC ACID is utilized in drug development as a potential lead compound for the creation of novel therapeutic agents. Its unique structural features may offer advantages in terms of selectivity, potency, and reduced side effects compared to existing treatments.
Used in Chiral Chemical Synthesis:
(R)-2-(TERT-BUTOXYCARBONYLAMINO)-2-((1R,4R)-4-HYDROXYCYCLOHEXYL)ACETIC ACID is employed as a chiral building block in the synthesis of enantioselective chemical reactions, providing a means to obtain enantiomerically pure products, which is essential for the development of single-enantiomer drugs with fewer side effects.
Used in Bioactive Compounds Synthesis:
In the synthesis of biologically active compounds, (R)-2-(TERT-BUTOXYCARBONYLAMINO)-2-((1R,4R)-4-HYDROXYCYCLOHEXYL)ACETIC ACID is used as a precursor to create molecules with specific biological activities, such as agonists or antagonists of certain receptors, or as modulators of enzymatic activity.

Check Digit Verification of cas no

The CAS Registry Mumber 130624-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,2 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 130624-89:
(8*1)+(7*3)+(6*0)+(5*6)+(4*2)+(3*4)+(2*8)+(1*9)=104
104 % 10 = 4
So 130624-89-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H23NO5/c1-13(2,3)19-12(18)14-10(11(16)17)8-4-6-9(15)7-5-8/h8-10,15H,4-7H2,1-3H3,(H,14,18)(H,16,17)/t8-,9-,10?

130624-89-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-hydroxycyclohexyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid

1.2 Other means of identification

Product number -
Other names 2-(4-hydroxycyclohexyl)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]acetic 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:130624-89-4 SDS

130624-89-4Relevant academic research and scientific papers

Synthesis of Optically Pure Analogue of D-Arginine Methyl Ester with Antiarrhythmic Activity

Banfi, Aldo,Benedini, Francesca,Sala, Alberto,Russo, Giovanni

, p. 3585 - 3597 (2007/10/02)

The synthesis of the methyl esters of optically pure trans and cis 4-guanidinocyclohexylglycine as rigid analogues of D-arginine methyl ester are described.

Synthesis of Optically Pure Analogues of D-Arginine Methyl Ester with Antiarrhythmic Activity

Banfi, Aldo,Benedini, Francesca,Sala, Alberto

, p. 1531 - 1542 (2007/10/02)

The synthesis of the methyl esters of optically pure trans and cis 4-guanidinocyclohexylglycine as rigid analogues of D-arginine methyl ester are described.

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