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120811-32-7

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120811-32-7 Usage

General Description

2H-PYRAN-3-AMINE, TETRAHYDRO- is a chemical compound with the molecular formula C5H9NO. It is a derivative of pyran, a six-membered heterocyclic compound containing oxygen and nitrogen atoms. 2H-PYRAN-3-AMINE, TETRAHYDRO- is also known as tetrahydropyran-3-amine and is commonly used in organic synthesis and medicinal chemistry. It has potential applications in the development of pharmaceuticals and agrochemicals due to its diverse reactivity and biological activity. Additionally, 2H-PYRAN-3-AMINE, TETRAHYDRO- may also be utilized as a building block in the synthesis of various complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 120811-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,8,1 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 120811-32:
(8*1)+(7*2)+(6*0)+(5*8)+(4*1)+(3*1)+(2*3)+(1*2)=77
77 % 10 = 7
So 120811-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO/c6-5-2-1-3-7-4-5/h5H,1-4,6H2

120811-32-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name oxan-3-amine

1.2 Other means of identification

Product number -
Other names tetrahydropyran-3-ylamine

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:120811-32-7 SDS

120811-32-7Upstream product

120811-32-7Downstream Products

120811-32-7Relevant articles and documents

Direct Access to Primary Amines from Alkenes by Selective Metal-Free Hydroamination

Du, Yi-Dan,Chen, Bi-Hong,Shu, Wei

supporting information, p. 9875 - 9880 (2021/03/29)

Direct and selective synthesis of primary amines from easily available precursors is attractive yet challenging. Herein, we report the rapid synthesis of primary amines from alkenes via metal-free regioselective hydroamination at room temperature. Ammonium carbonate was used as ammonia surrogate for the first time, allowing for efficient conversion of terminal and internal alkenes into linear, α-branched, and α-tertiary primary amines under mild conditions. This method provides a straightforward and powerful approach to a wide spectrum of advanced, highly functionalized primary amines which are of particular interest in pharmaceutical chemistry and other areas.

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