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90322-18-2

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90322-18-2 Usage

General Description

3-[(Tetrahydrofuran-2-ylmethyl)amino]propanenitrile is a chemical compound with the molecular formula C8H14N2O. It is a colorless liquid with a faint odor and is commonly used as a building block in organic synthesis. 3-[(TETRAHYDROFURAN-2-YLMETHYL)AMINO]PROPANENITRILE is derived from tetrahydrofuran, which is a cyclic ether commonly used as a solvent in organic reactions. The presence of a nitrile group in the molecule makes it useful for the synthesis of various pharmaceuticals and agrochemicals. Its properties and versatility make it a valuable component in the production of many different types of chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 90322-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,2 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90322-18:
(7*9)+(6*0)+(5*3)+(4*2)+(3*2)+(2*1)+(1*8)=102
102 % 10 = 2
So 90322-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H14N2O/c9-4-2-5-10-7-8-3-1-6-11-8/h8,10H,1-3,5-7H2

90322-18-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(oxolan-2-ylmethylamino)propanenitrile

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:90322-18-2 SDS

90322-18-2Relevant articles and documents

Aryl sulfonamides as selective PDE4 inhibitors

Montana, John G.,Buckley, George M.,Cooper, Nicola,Dyke, Hazel J.,Gowers, Lewis,Gregory, Joanna P.,Hellewell, Paul G.,Kendall, Hannah J.,Lowe, Christopher,Maxey, Robert,Miotla, Jadwiga,Naylor, Robert J.,Runcie, Karen A.,Tuladhar, Bishwa,Warneck, Julie B. H.

, p. 2635 - 2640 (2007/10/03)

A series of novel selective phosphodiesterase 4 (PDE4) inhibitors has been developed which displays activity both in vitro and in vivo. These compounds possess good selectivity for the catalytic site of PDE4 over the high affinity Rolipram binding site. In vivo studies demonstrate a reduced propensity to display the emetic side effects which are commonly observed with PDE4 inhibitors.

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