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3-(4-difluoromethoxy-phenyl)-propionic acid is a chemical compound with the molecular formula C10H9F2O3. It is a derivative of propionic acid, featuring a difluoromethoxy group attached to a phenyl ring. 3-(4-difluoromethoxy-phenyl)-propionic acid is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs. Its structure allows for the exploration of its properties in drug design, such as its ability to interact with biological targets due to the presence of the difluoromethoxy group, which can influence its lipophilicity and binding affinity. The compound's synthesis and characterization are of interest to chemists and pharmacologists alike, as it may contribute to the development of new therapeutic agents.

1000932-18-2

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1000932-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1000932-18-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,9,3 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1000932-18:
(9*1)+(8*0)+(7*0)+(6*0)+(5*9)+(4*3)+(3*2)+(2*1)+(1*8)=82
82 % 10 = 2
So 1000932-18-2 is a valid CAS Registry Number.

1000932-18-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[4-(Difluoromethoxy)phenyl]propanoic acid

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:1000932-18-2 SDS

1000932-18-2Relevant academic research and scientific papers

Structure-activity relationship studies and sleep-promoting activity of novel 1-chloro-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine derivatives as dual orexin receptor antagonists. Part 2

Sifferlen, Thierry,Koberstein, Ralf,Cottreel, Emmanuelle,Boller, Amandine,Weller, Thomas,Gatfield, John,Brisbare-Roch, Catherine,Jenck, Francois,Boss, Christoph

, p. 3857 - 3863 (2013/07/27)

Replacement of the dimethoxyphenyl moiety in the core skeleton of almorexant by appropriately substituted imidazoles afforded novel 1-chloro-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine derivatives as potent dual orexin receptor antagonists. We describe in th

5,6,7,8-TETRAHYDRO-IMIDAZO[1,5-A]PYRAZINE COMPOUNDS

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Page/Page column 18, (2011/05/08)

The invention relates to 5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine derivatives of formula (I) wherein R1, R2, R3, and R4 are as described n the description, to salts, especially pharmaceutically acceptable salts thereof, and to the use of such compounds as medicaments; especially as orexin receptor antagonists.

5,6,7,8-TETRAHYDRO-IMIDAZO[1,5-A]PYRAZINE COMPOUNDS

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Page/Page column 37, (2010/01/30)

The invention relates to 5,6,7,8-tetrahydro-imidazo[1,5- a]pyrazine derivatives of formula (I) wherein R1, R2, R3, and R4 are as described n the description, to salts, especially pharmaceutically acceptable salts thereof, and to the use of such compounds as medicaments; especially as orexin receptor antagonists.

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