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(1S,3S)-3-Hydroxy-cyclopentanecarboxylic acid is a chiral cyclic organic compound with the molecular formula C6H10O3. It features a cyclopentane ring with a hydroxyl group and a carboxylic acid group attached, and possesses two stereocenters at the first and third carbon atoms. (1S,3S)-3-HYDROXY-CYCLOPENTANECARBOXYLIC ACID is widely utilized in organic synthesis and pharmaceutical research as a key building block for the creation of various biologically active molecules. Its unique structure and properties render it valuable in the development of innovative drugs and other significant organic compounds.

107983-78-8

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107983-78-8 Usage

Uses

Used in Pharmaceutical Research:
(1S,3S)-3-Hydroxy-cyclopentanecarboxylic acid is used as a key intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into the molecular structures of potential drug candidates. Its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial for ensuring the desired biological activity and minimizing side effects.
Used in Organic Synthesis:
In the field of organic synthesis, (1S,3S)-3-hydroxy-cyclopentanecarboxylic acid serves as a versatile building block for the construction of complex organic molecules. Its functional groups and cyclic structure facilitate various chemical reactions, making it a valuable component in the synthesis of a wide range of organic compounds.
Used in Drug Development:
(1S,3S)-3-Hydroxy-cyclopentanecarboxylic acid is utilized in drug development as a structural element in the design of new pharmaceutical agents. Its unique stereochemistry and reactivity contribute to the discovery of novel therapeutics with improved efficacy and selectivity.
Used in Chiral Chemistry:
In chiral chemistry, (1S,3S)-3-hydroxy-cyclopentanecarboxylic acid is employed as a chiral source for the synthesis of enantiomerically pure compounds. Its presence in the final product can influence the biological activity, making it an essential component in the development of enantioselective synthetic routes.
Used in the Synthesis of Biologically Active Compounds:
(1S,3S)-3-Hydroxy-cyclopentanecarboxylic acid is used as a precursor in the synthesis of biologically active compounds, such as natural products and pharmaceutical agents. Its incorporation into these molecules can enhance their potency, selectivity, and pharmacokinetic properties, leading to more effective treatments for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 107983-78-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,9,8 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 107983-78:
(8*1)+(7*0)+(6*7)+(5*9)+(4*8)+(3*3)+(2*7)+(1*8)=158
158 % 10 = 8
So 107983-78-8 is a valid CAS Registry Number.

107983-78-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,3S)-3-HYDROXY-CYCLOPENTANECARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:107983-78-8 SDS

107983-78-8Relevant academic research and scientific papers

CHEMOENZYMATIC SYNTHESIS OF CONFORMATIONALLY RIGID GLUTAMIC ACID ANALOGUES

Trigalo, F.,Buisson, D.,Azerad, R.

, p. 6109 - 6112 (2007/10/02)

All stereomers of cyclohexane cyclopentane-derived analogues of glutamic acid have been synthesized from the corresponding 3-keto-cycloalkyl carboxylic acid esters by a combination of microbial steps and standard chemical methods.

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