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1-[2-(Cyclopropylmethoxy)-6-hydroxyphenyl]ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

405239-70-5

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405239-70-5 Usage

Type of Drug

Non-steroidal anti-inflammatory drug (NSAID)

Usage

Veterinary medication for treating pain and inflammation in dogs and cats

Mechanism of Action

Inhibits the production of prostaglandins, which cause pain and inflammation

Effective for

Arthritis, post-operative pain, and other conditions causing discomfort in animals

Tolerance

Generally well-tolerated by pets when used according to prescribed dosage

Potential Side Effects

Gastrointestinal irritation, kidney and liver toxicity, and rare allergic reactions

Precaution

Pet owners should follow veterinarian's recommendations and monitor pets for adverse reactions when using carprofen

Check Digit Verification of cas no

The CAS Registry Mumber 405239-70-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,5,2,3 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 405239-70:
(8*4)+(7*0)+(6*5)+(5*2)+(4*3)+(3*9)+(2*7)+(1*0)=125
125 % 10 = 5
So 405239-70-5 is a valid CAS Registry Number.

405239-70-5SDS

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-[2-(Cyclopropylmethoxy)-6-hydroxyphenyl]ethanone

1.2 Other means of identification

Product number -
Other names 1-(2-(cyclopropylmethoxy)-6-hydroxyphenyl)ethanone

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:405239-70-5 SDS

405239-70-5Relevant academic research and scientific papers

2-AMINOPYRIDINE DERIVATIVE

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Page/Page column 15; 23, (2010/11/25)

The invention relates to a compound useful as remedies or preventives for IKK2-related inflammatory diseases or autoimmune diseases, or that is, a 2-aminopyrimidine derivative having a 2-hydroxyphenyl group at the 6-position thereof and having a saturated

Synthesis and structure-activity relationships of novel IKK-β inhibitors. Part 3: Orally active anti-inflammatory agents

Murata, Toshiki,Shimada, Mitsuyuki,Sakakibara, Sachiko,Yoshino, Takashi,Masuda, Tsutomu,Shintani, Takuya,Sato, Hiroki,Koriyama, Yuji,Fukushima, Keiko,Nunami, Noriko,Yamauchi, Megumi,Fuchikami, Kinji,Komura, Hiroshi,Watanabe, Akihiko,Ziegelbauer, Karl B.,Bacon, Kevin B.,Lowinger, Timothy B.

, p. 4019 - 4022 (2007/10/03)

A series of 2-amino-3-cyano-4-alkyl-6-(2-hydroxyphenyl)pyridine derivatives was synthesized and evaluated as IκB kinase β (IKK-β) inhibitors. Modification of a novel IKK-β inhibitor 1 (IKK-β IC 50=1500nM, Cell IC50=8000nM) at the 4-p

4-6-Diphenyl pyridine derivatives as antiinflammatory agents

-

, (2008/06/13)

4-aryl pyrimidine compounds of general formula and salts thereof: wherein X is CH or N; R1 is hydrogen, halogen, C1-6 alkyl, C1-6 alkoxy, etc.; R2 is hydrogen or hydroxy; R3 is hydrogen, C1-6 alkyl, etc.; R4 is hydrogen, hydroxy, halogen, amino, etc.; R5

AN OPTICALLY ACITVE PYRIDINE DERIVATIVE AND A MEDICAMENT CONTAINING THE SAME

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Page/Page column 26-27, (2008/06/13)

An optically active (-)-7-[2-(cyclopropylmethoxy)-6-hydroxyphenyl]-5-[(3S)-3-piperidinyl]-1,4-dihydro-2H-pyrido [2,3-d][1,3]oxazin-2-one of the formula (I) or salt thereof. The compound has an excellent anti-inflammatory activity, and other biological act

Pyridine derivatives

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, (2008/06/13)

Pyridine compounds of general formula: wherein —R1represents in which R11is hydrogen, C1-6alkyl, halogen, hydroxy, C1-12alkoxy, nitro, amino, C1-6alkylsulfonylamino, C1-6alkoxycarbonyl, C1-6alkylamino, di(C1-6alkyl)amino, C1-6alkanoylamino, phenyl C1-6alkylamino, phenylsulfonylamino, or —O—(CH2)n—R111; R2represents hydrogen or halogen; R3represents hydrogen, —CR31R32R33, or —NR34R35; R4is hydrogen, carbamoyl, CN, carboxyl, etc.; R5is amino, C1-6alkylamino, di C1-6alkylamino, etc. or salt thereof. The compound has an excellent anti-inflammatory activity, and other biological activity.

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