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127320-83-6

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127320-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127320-83-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,3,2 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 127320-83:
(8*1)+(7*2)+(6*7)+(5*3)+(4*2)+(3*0)+(2*8)+(1*3)=106
106 % 10 = 6
So 127320-83-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H18N2O/c1-2-5-11(4-1)7-9-8-12-6-3-10-9/h9-10H,1-8H2

127320-83-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(pyrrolidin-1-ylmethyl)morpholine

1.2 Other means of identification

Product number -
Other names 3-PYRROLIDIN-1-YLMETHYL-MORPHOLINE

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:127320-83-6 SDS

127320-83-6Downstream Products

127320-83-6Relevant articles and documents

2-Aminomethyl piperidines as novel urotensin-II receptor antagonists

Jin, Jian,Wang, Yonghui,Wang, Feng,Shi, Dongchuan,Erhard, Karl F.,Wu, Zining,Guida, Brian F.,Lawrence, Sarah K.,Behm, David J.,Disa, Jyoti,Vaidya, Kalindi S.,Evans, Christopher,McMillan, Lynette J.,Rivero, Ralph A.,Neeb, Michael J.,Douglas, Stephen A.

, p. 2860 - 2864 (2008/12/22)

A series of 2-aminomethyl piperidines has been discovered as novel urotensin-II receptor antagonists. The synthesis, initial structure-activity relationships, and optimization of the initial hit that resulted in the identification of potent, cross-species active, and functional urotensin-II receptor antagonists such as 1a and 11a are described.

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