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919995-27-0

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919995-27-0 Usage

General Description

1-(4-methoxy-3-(3-methoxypropoxy)phenyl)-3-methylbutan-1-one is a chemical compound with the molecular formula C18H26O4. It is an organic compound that belongs to the ketone functional group and contains a phenyl ring with a methoxy group and a propoxy group attached to it. It also contains a butanone group with a methyl substituent. 1-(4-methoxy-3-(3-methoxypropoxy)phenyl)-3-methylbutan-1-one has potential applications in the pharmaceutical and chemical industries for its unique structure and properties. It is important to handle and use this chemical with caution, as it may have potential health and safety hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 919995-27-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,9,9,9 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 919995-27:
(8*9)+(7*1)+(6*9)+(5*9)+(4*9)+(3*5)+(2*2)+(1*7)=240
240 % 10 = 0
So 919995-27-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H24O4/c1-12(2)10-14(17)13-6-7-15(19-4)16(11-13)20-9-5-8-18-3/h6-7,11-12H,5,8-10H2,1-4H3

919995-27-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-Methoxy-3-(3-Methoxypropoxy)Phenyl)-3-Methylbutan-1-One

1.2 Other means of identification

Product number -
Other names 1-[4-methoxy-3-(3-methoxypropoxy)phenyl]-3-methylbutan-1-one

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:919995-27-0 SDS

919995-27-0Relevant articles and documents

A new approach to the synthesis of peptidomimetic renin inhibitors: Palladium-catalyzed asymmetric allylation of acyclic alkyl aryl ketones

Hanessian, Stephen,Chénard, Etienne

supporting information; experimental part, p. 3222 - 3225 (2012/08/08)

A new approach to the synthesis of Tekturna, a recently marketed drug for hypertension, takes advantage of a modified protocol of the Stoltz palladium-catalyzed asymmetric allylation with a t-BuPHOX ligand for the synthesis of allylated acyclic alkyl aryl

NEW PYROCATECHIN DERIVATIVES

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Page/Page column 18, (2008/06/13)

Pyrocatechin derivatives of formula I wherein R illustrates a group of formulae Ia, Ib, Ic or Id R1 is 4-halogen-but-2-enyl, R2 is lower alkyl or cycloalkyl, R3 is lower alkoxy and R4 is lower alkoxy lower alkox

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