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(S)-4-benzyl-2-hydroxymethylpiperazine is a chiral piperazine derivative characterized by the presence of a benzyl group and a hydroxymethyl group attached to its piperazine ring. As a member of the piperazine class, it has been investigated for various pharmacological activities, such as antiviral, antipsychotic, and antihistaminic properties. The specific stereochemistry denoted by "(S)" is crucial for its potential applications, which are still under exploration.

149715-45-7

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149715-45-7 Usage

Uses

Used in Pharmaceutical Industry:
(S)-4-benzyl-2-hydroxymethylpiperazine is used as a precursor in the synthesis of various pharmaceutical compounds due to its unique structural features and chirality. Its potential as an antiviral, antipsychotic, or antihistaminic agent is being studied, highlighting its importance in drug development.
Used in Chemical Research:
In the field of chemical research, (S)-4-benzyl-2-hydroxymethylpiperazine serves as a model compound for understanding the effects of stereochemistry on biological activity. Its unique structure allows researchers to explore the relationship between molecular configuration and pharmacological efficacy.
Used in Drug Development:
(S)-4-benzyl-2-hydroxymethylpiperazine is utilized in drug development as a lead compound for the discovery of new therapeutic agents. Its potential applications in treating various conditions, such as viral infections, mental health disorders, and allergic reactions, make it a valuable asset in the search for novel medications.

Check Digit Verification of cas no

The CAS Registry Mumber 149715-45-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,7,1 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 149715-45:
(8*1)+(7*4)+(6*9)+(5*7)+(4*1)+(3*5)+(2*4)+(1*5)=157
157 % 10 = 7
So 149715-45-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H18N2O/c15-10-12-9-14(7-6-13-12)8-11-4-2-1-3-5-11/h1-5,12-13,15H,6-10H2/t12-/m0/s1

149715-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2S)-4-benzylpiperazin-2-yl]methanol

1.2 Other means of identification

Product number -
Other names (S)-(4-Benzylpiperazin-2-yl)methanol

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:149715-45-7 SDS

149715-45-7Relevant articles and documents

COMPOUNDS THAT INHIBIT MCL-1 PROTEIN

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, (2018/10/25)

Provided herein are myeloid cell leukemia 1 protein (Mcl-1) inhibitors, methods of their preparation, related pharmaceutical compositions, and methods of using the same. For example, provided herein are compounds of Formula (I), or a stereoisomer thereof; and pharmaceutically acceptable salts thereof and pharmaceutical compositions containing the compounds. The compounds and compositions provided herein may be used, for example, in the treatment of diseases or conditions, such as cancer.

Carbostyril carboxylic compounds and intermediates, preparation method and application thereof

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Paragraph 0146; 0150, (2017/07/12)

The invention discloses carbostyril carboxylic compounds and hydrochlorides thereof and also discloses a preparation method of the compounds and the hydrochlorides thereof as well as an application of the compounds and the hydrochlorides thereof in preparing gram-positive bacterium-preventing or gram-negative bacterium-preventing drugs. Moreover, the invention discloses intermediates for preparing the compounds and a preparation method of the intermediates.

Enantiomerically pure 2-piperazinemethanols as novel chiral ligands of oxazaborolidine catalysts in enantioselective borane reductions

Inoue, Tsutomu,Sato, Daisuke,Komura, Kenichi,Itsuno, Shinichi

, p. 5379 - 5382 (2007/10/03)

Novel enantiomerically pure 2-piperazinemethanols (3-5) were synthesized from 2-piperazinecarboxylic acid 1. The asymmetric reduction of aromatic ketones, ketimine and oxime ether has been performed with reagents prepared from 2-piprazinemethanol and borane to yield enantiomerically enriched alcohols and amines, respectively. The preferred absolute configuration of the product was dependent on the structure of the sulfonyl substituent in the chiral ligand.

A potent new class of κ-receptor agonist: 4-Substituted 1-(arylacetyl)- 2-[(dialkylamino)methyl]piperazines

Naylor,Judd,Lloyd,Scopes,Hayes,Birch

, p. 2075 - 2083 (2007/10/02)

The synthesis of 4-substituted 1-(arylacetyl)-2- [(alkylamino)methyl]piperazines (10-22, 26, 27, and 30-33) and their activities as κ-opioid receptor agonists are described. This includes a range of 4-acyl and 4-carboalkoxy derivatives with the latter ser

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