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100841-00-7

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100841-00-7 Usage

General Description

3-(4-methoxyphenoxy)propan-1-amine, also known as 2-(4-methoxyphenoxy)propan-1-amine or PPG-14 butyl ether, is a chemical compound with the molecular formula C10H15NO2. It belongs to the class of amines and is derived from propan-1-amine. It is commonly used as an ingredient in various personal care and cosmetic products, suchagent for liquid household and personal care products, as well as an ingredient in lubricants and paints. It is also sometimes used as a fragrance ingredient in perfumes and colognes.

Check Digit Verification of cas no

The CAS Registry Mumber 100841-00-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,4 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100841-00:
(8*1)+(7*0)+(6*0)+(5*8)+(4*4)+(3*1)+(2*0)+(1*0)=67
67 % 10 = 7
So 100841-00-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO2/c1-12-9-3-5-10(6-4-9)13-8-2-7-11/h3-6H,2,7-8,11H2,1H3

100841-00-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methoxyphenoxy)propan-1-amine

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:100841-00-7 SDS

100841-00-7Relevant articles and documents

Antitumour indolequinones: Synthesis and activity against human pancreatic cancer cells

Inman, Martyn,Visconti, Andrea,Yan, Chao,Siegel, David,Ross, David,Moody, Christopher J.

, p. 4848 - 4861 (2014/07/07)

An important determinant of the growth inhibitory activity of indolequinones against pancreatic cancer cells is substitution on the 2-position with 2-unsubstituted derivatives being markedly more potent. A series of indolequinones bearing a range of subst

PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE PPAR-ACTIVATING COMPOUND AND INTERMEDIATE OF THE SAME

-

, (2008/06/13)

A process for obtaining a compound (1) and an intermediate thereof in high yield and high optical yield is provided. A process for producing a compound (4), the process including reacting a compound (2) with a compound (3) in the presence of a base; and a process for producing a compound (1), the process including reacting a compound (2) with a compound (3) in the presence of a base to yield a compound (4) and then deesterifying the compound (4). wherein R represents an alkyl group having 1 to 6 carbon atoms or an aralkyl group having 7 to 8 carbon atoms.

Design and synthesis of highly potent and selective human peroxisome proliferator-activated receptor α agonists

Yamazaki, Yukiyoshi,Abe, Kazutoyo,Toma, Tsutomu,Nishikawa, Masahiro,Ozawa, Hidefumi,Okuda, Ayumu,Araki, Takaaki,Oda, Soichi,Inoue, Keisuke,Shibuya, Kimiyuki,Staels, Bart,Fruchart, Jean-Charles

, p. 4689 - 4693 (2008/02/11)

A combination of benzoxazole, phenoxyalkyl side chain, and phenoxybutyric acids was identified as a highly potent and selective human peroxisome proliferator-activated receptor α (PPARα) agonist. The synthesis, structure-activity relationship (SAR) studies, and in vivo activities of the representative compounds are described.

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