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(S)-Tetrahydro-2H-pyran-3-amine hydrochloride is a chemical compound with the molecular formula C5H11NO?HCl, characterized as a white solid with a molecular weight of 143.60 g/mol. It belongs to the class of amines and is recognized for its role as a building block in organic synthesis. (S)-Tetrahydro-2H-pyran-3-amine hydrochloride is also a key intermediate in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. The hydrochloride salt form enhances its solubility in water, facilitating its use in a variety of chemical reactions and formulations. Additionally, (S)-Tetrahydro-2H-pyran-3-amine hydrochloride exhibits potential biological activity, positioning it as a valuable component in the research and development of new drugs and therapies.

1245724-46-2

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1245724-46-2 Usage

Uses

Used in Organic Synthesis:
(S)-Tetrahydro-2H-pyran-3-amine hydrochloride is used as a building block in organic synthesis for its ability to contribute to the formation of complex organic molecules, which are essential in various chemical and pharmaceutical applications.
Used in Pharmaceutical Preparation:
As a key intermediate, (S)-Tetrahydro-2H-pyran-3-amine hydrochloride is utilized in the development and production of pharmaceuticals, playing a crucial role in the synthesis of active pharmaceutical ingredients.
Used in Agrochemical Production:
(S)-Tetrahydro-2H-pyran-3-amine hydrochloride also serves as an intermediate in the preparation of agrochemicals, contributing to the development of products that enhance crop protection and yield.
Used in Fine Chemicals Industry:
(S)-Tetrahydro-2H-pyran-3-amine hydrochloride is employed in the manufacture of fine chemicals, which are high-purity chemicals used in various industries, including pharmaceuticals, fragrances, and flavors.
Used in Research and Development of New Drugs and Therapies:
Due to its potential biological activity, (S)-Tetrahydro-2H-pyran-3-amine hydrochloride is used in research and development for exploring its applications in new drug discovery and therapeutic interventions.

Check Digit Verification of cas no

The CAS Registry Mumber 1245724-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,7,2 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1245724-46:
(9*1)+(8*2)+(7*4)+(6*5)+(5*7)+(4*2)+(3*4)+(2*4)+(1*6)=152
152 % 10 = 2
So 1245724-46-2 is a valid CAS Registry Number.

1245724-46-2SDS

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 (S)-Tetrahydro-2H-pyran-3-amine hydrochloride

1.2 Other means of identification

Product number -
Other names (3S)-oxan-3-amine,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:1245724-46-2 SDS

1245724-46-2Relevant academic research and scientific papers

TRICYCLIC HETEROCYCLIC COMPOUNDS, COMPOSITIONS AND METHODS OF USE THEREOF AS JAK INHIBITORS

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Page/Page column 110; 111, (2013/03/26)

The invention provides novel compounds of formula I having the general formula:(I) wherein Rl s R2, R3, X and Y are as described herein. Accordingly, the compounds may be provided in pharmaceutically acceptable compositions and used for the treatment of immunological or hyperproliferative disorders.

Kilogram synthesis of (S)-3-aminopyran from l -glutamic acid

Savage, Scott,Babu, Srinivasan,Zak, Mark,Mao, Zhongping,Cao, Jianhua,Ge, Yonghui,Ma, Dongxu,Jiang, Guoqiang

, p. 987 - 990 (2013/07/05)

We describe the development of a concise route to prepare kilogram quantities of (S)-3-aminopyran, a key intermediate in the synthesis of a Jak1 inhibitor. The chiral amine was introduced via a chiral-pool approach and involves using inexpensive, commerci

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