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120958-90-9

120958-90-9

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120958-90-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120958-90-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,9,5 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 120958-90:
(8*1)+(7*2)+(6*0)+(5*9)+(4*5)+(3*8)+(2*9)+(1*0)=129
129 % 10 = 9
So 120958-90-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H29N3O2/c1-2-19-18(22)20-10-7-13-23-17-9-6-8-16(14-17)15-21-11-4-3-5-12-21/h6,8-9,14H,2-5,7,10-13,15H2,1H3,(H2,19,20,22)

120958-90-9SDS

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 1-ethyl-3-[3-[3-(piperidin-1-ylmethyl)phenoxy]propyl]urea

1.2 Other means of identification

Product number -
Other names KU 1257

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:120958-90-9 SDS

120958-90-9Downstream Products

120958-90-9Relevant articles and documents

Synthesis and antiulcer activity of N-substituted N'-[3-[3- (piperidinomethyl)phenoxy]propyl]ureas: Histamine H2-receptor antagonists with a potent mucosal protective activity

Miyashita,Matsumoto,Matsukubo,Iinuma,Taga,Sekiguchi,Hamada,Okamura,Nishino

, p. 2446 - 2451 (2007/10/02)

As an aim toward developing new antiulcer agents, new N-substituted N'-[3- [3-(piperidinomethyl)phenoxy]propyl]ureas were synthesized and evaluated for histamine H2-receptor antagonistic, gastric antisecretory, and gastric mucosal protective activities. A QSAR study showed that the most favorable N- substituents were electron-donating straight-chain alkyl groups of short length such as ethyl group from the viewpoint of dual action, i.e., gastric antisecretory and mucosal protective actions. Among the ureas studied, compounds 4, 5, and 8-10 were selected as candidates for further study.

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