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(R)-1-Amino-3-chloro-2-propanol hydrochloride, a chiral building block with the molecular formula C3H8ClNO·HCl, is a derivative of the amino alcohol. Its hydrochloride salt form enhances its stability and water solubility, making it a versatile compound in the synthesis of pharmaceuticals and agrochemicals. It is often utilized as a reagent in organic synthesis for the production of various pharmaceutical compounds and as a chiral auxiliary in asymmetric synthesis. Additionally, it can be used as a resolving agent for the separation of racemic mixtures, playing a significant role in drug development and organic chemistry research.

34839-14-0

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34839-14-0 Usage

Uses

Used in Pharmaceutical Industry:
(R)-1-Amino-3-chloro-2-propanol hydrochloride is used as a chiral building block for the synthesis of pharmaceutical compounds. Its unique stereochemistry allows for the creation of enantiomerically pure drugs, which is crucial for ensuring the desired therapeutic effects and minimizing potential side effects.
Used in Agrochemical Industry:
(R)-1-Amino-3-chloro-2-propanol hydrochloride is used as a chiral building block in the synthesis of agrochemicals. Its ability to create enantiomerically pure compounds can lead to the development of more effective and environmentally friendly pesticides and herbicides.
Used in Organic Synthesis:
(R)-1-Amino-3-chloro-2-propanol hydrochloride is used as a reagent in organic synthesis for the production of various pharmaceutical compounds. Its hydrochloride salt form improves its solubility, facilitating its use in a wide range of chemical reactions.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
(R)-1-Amino-3-chloro-2-propanol hydrochloride is used as a chiral auxiliary in asymmetric synthesis. Its unique stereochemistry helps to control the stereoselectivity of chemical reactions, enabling the synthesis of enantiomerically pure compounds with high yields and selectivity.
Used as a Resolving Agent for Racemic Mixtures:
(R)-1-Amino-3-chloro-2-propanol hydrochloride is used as a resolving agent for the separation of racemic mixtures. Its ability to selectively interact with enantiomers allows for the efficient separation of chiral compounds, which is essential for the production of enantiomerically pure drugs and other chiral molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 34839-14-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,3 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34839-14:
(7*3)+(6*4)+(5*8)+(4*3)+(3*9)+(2*1)+(1*4)=130
130 % 10 = 0
So 34839-14-0 is a valid CAS Registry Number.

34839-14-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-1-Amino-3-chloro-2-propanol hydrochloride

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:34839-14-0 SDS

34839-14-0Upstream product

34839-14-0Downstream Products

34839-14-0Relevant academic research and scientific papers

SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINE COMPOUNDS AS TRK KINASE INHIBITORS

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Page/Page column 140, (2011/02/24)

Compounds of Formula (I) and salts thereof in which R1, R2, R3, R4, X, Y and n have the meanings given in the specification, are inhibitors of Trk kinases and are useful in the treatment of diseases which can be treated with a Trk kinase inhibitor such as pain, cancer, inflammation, neurodegenerative diseases and certain infectious diseases.

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