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(3R,4R)-rel-3,4-Piperidinediol Hydrochloride is a hydroxylated piperidine derivative, characterized by its unique stereochemistry and functional groups. It serves as a key intermediate in the synthesis of various pharmaceutical and biologically active compounds due to its versatile chemical properties and potential for further functionalization.

443648-97-3

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443648-97-3 Usage

Uses

Used in Pharmaceutical Synthesis:
(3R,4R)-rel-3,4-Piperidinediol Hydrochloride is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its unique stereochemistry and functional groups make it a valuable building block for the development of new drugs with potential therapeutic applications.
Used in Biologically Active Compounds Synthesis:
(3R,4R)-rel-3,4-Piperidinediol Hydrochloride is also used as a starting material for the synthesis of biologically active compounds. Its structural features allow for the creation of molecules with specific biological activities, which can be further optimized for various therapeutic purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 443648-97-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,6,4 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 443648-97:
(8*4)+(7*4)+(6*3)+(5*6)+(4*4)+(3*8)+(2*9)+(1*7)=173
173 % 10 = 3
So 443648-97-3 is a valid CAS Registry Number.

443648-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4S)-3,4-Piperidinediol hydrochloride (1:1)

1.2 Other means of identification

Product number -
Other names (3R,4R)-rel-3,4-Piperidinediol Hydrochloride

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:443648-97-3 SDS

443648-97-3Downstream Products

443648-97-3Relevant academic research and scientific papers

Synthesis, molecular modeling and evaluation of α-glucosidase inhibition activity of 3,4-dihydroxy piperidines

Kasturi, Siva Prasad,Surarapu, Sujatha,Uppalanchi, Srinivas,Dwivedi, Shubham,Yogeeswari, Perumal,Sigalapalli, Dilep Kumar,Bathini, Nagendra Babu,Ethiraj, Krishna S.,Anireddy, Jaya Shree

, p. 39 - 52 (2018)

Biological evaluation of 3,4-dihydroxy piperidines as α-glucosidase inhibitors is being reported for the first time. Forty-five derivatives (amides, di-amides and sulfonamides) were made using cis and trans 3,4-dihydroxy piperidines to evaluate their α-glucosidase inhibition activity. Polar groups (-OH, -NH2) on phenyl ring having derivatives 5i, 5l, 7g, 7i & 12j showed excellent activity compared to standard references. Acarbose, Voglibose and Miglitol were used as standard references. Molecular docking simulations were done for compounds to identify important binding modes responsible for inhibition activity of α-glucosidase.

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