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33024-60-1

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33024-60-1 Usage

General Description

4-Aminotetrahydropyran hydrochloride is a chemical compound that belongs to the class of amines. It is an organic compound with the molecular formula C5H12ClNO and a molecular weight of 137.60 g/mol. 4-Aminotetrahydropyran hydrochloride is commonly used as a precursor in the synthesis of various pharmaceuticals and organic compounds. It is a white to off-white crystalline powder that is soluble in water and ethanol. 4-Aminotetrahydropyran hydrochloride has a wide range of applications in the pharmaceutical industry, including as a building block for the synthesis of drugs and as a reagent in organic chemistry reactions. Its versatility and broad range of applications make it a valuable compound in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 33024-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,2 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 33024-60:
(7*3)+(6*3)+(5*0)+(4*2)+(3*4)+(2*6)+(1*0)=71
71 % 10 = 1
So 33024-60-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO.ClH/c6-5-1-3-7-4-2-5;/h5H,1-4,6H2;1H

33024-60-1SDS

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 4-Aminotetrahydropyran hydrochloride

1.2 Other means of identification

Product number -
Other names ATHP-HCL

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:33024-60-1 SDS

33024-60-1Relevant articles and documents

Cross-Coupling of Alkyl Redox-Active Esters with Benzophenone Imines: Tandem Photoredox and Copper Catalysis

Mao, Runze,Balon, Jonathan,Hu, Xile

, p. 9501 - 9504 (2018/07/29)

Alkyl amines are an important class of organic compounds in medicinal and materials chemistry. Until now very have been very few methods for the synthesis of alkyl amines by metal-catalyzed cross-coupling of alkyl electrophiles with nitrogen nucleophiles. Described here is an approach to employ tandem photoredox and copper catalysis to enable the cross-coupling of alkyl N-hydroxyphthalimide esters, readily derived from alkyl carboxylic acids, with benzophenone-derived imines. Hydrolysis of the coupling products furnish alkylated primary amines. Primary, secondary, and tertiary alkyl groups can be transferred, and the coupling tolerates a diverse set of functional groups. The method allows rapid functionalization of natural products and drugs, and can be used to expedite syntheses of pharmaceuticals from readily available chemical feedstocks.

PYRIDO-PYRIDIMIDINE DERIVATIVES USEFUL AS ANTIINFLAMMATORY AGENTS

-

Page/Page column 42, (2008/06/13)

Provided are novel pyrido-pyrimidine derivatives, having the structure of Formula (I): which can be used as anti-inflammatory agents. Also provided are pharmaceutical compositions comprising one or more pyrido-pyrimidine derivatives, as well as methods of

PROCESS FOR PRODUCTION OF 4-AMINOTETRAHYDROPYRANS AND SALTS THEREOF WITH ACIDS, INTERMEDIATES FOR THE PROCESS, AND PROCESS FOR PRODUCTION THEREOF

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Page/Page column 8, (2008/06/13)

The present invention relates to a process for preparing 4-aminotetrahydropyran compound and an acid salt thereof represented by the formula (2): wherein R represents a hydrogen atom or a hydrocarbon group, which comprises subjecting a 4-hydrazinotetrahydropyran compound or an acid salt thereof represented by the formula (1) : wherein R has the same meaning as defined above, to decomposition reaction in the presence of at least one compound selected from Raney nickel, noble metal catalyst and metal oxide, and a synthetic intermediate thereof and a process for preparing the same.

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