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63635-26-7

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63635-26-7 Usage

General Description

2-Isopropoxybenzoic acid, also known as ibuprofen, is a non-steroidal anti-inflammatory drug (NSAID) that is commonly used to relieve pain, reduce fever, and decrease inflammation. It works by inhibiting the production of prostaglandins, which are responsible for causing pain and inflammation in the body. Ibuprofen is widely used to alleviate symptoms of conditions such as arthritis, menstrual cramps, headaches, and minor injuries. It is available over-the-counter in various forms, including tablets, gels, and liquids, and is generally considered to be safe and effective when used as directed. However, prolonged or excessive use of ibuprofen can lead to serious side effects, including stomach bleeding, kidney damage, and cardiovascular issues, so it should be used with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 63635-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,3 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63635-26:
(7*6)+(6*3)+(5*6)+(4*3)+(3*5)+(2*2)+(1*6)=127
127 % 10 = 7
So 63635-26-7 is a valid CAS Registry Number.

63635-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-propan-2-yloxybenzoic acid

1.2 Other means of identification

Product number -
Other names 2-isopropoxy-benzoic acid

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:63635-26-7 SDS

63635-26-7Relevant articles and documents

MODIFIED PROTEINS AND PROTEIN DEGRADERS

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Paragraph 00525; 00528; 00529, (2021/12/08)

Provided herein are compounds, pharmaceutical compositions, and methods for binding or degrading target proteins. Further provided herein are compounds having a DNA damage-binding protein 1 (DDB1) binding moiety. Some such embodiments include a linker. Some such embodiments include a target protein binding moiety. Further provided herein are ligand-DDB1 complexes. Further provided herein are in vivo modified DDB1 proteins.

High diastereoselectivity in the yang photocyclization via remote hydrogen abstraction reaction

Jang, Mi,Park, Bong Ser

, p. 1509 - 1514 (2016/10/09)

1-Benzoyl-1-(o-alkoxyphenyl)cyclopropanes undergo Yang photocyclization to form dihydrobenzopyranols in a stereospecific manner. The cyclopropyl group at alpha position to carbonyls gives not only a bias in the most stable geometries of the starting ketones but also conformational restriction on geometries of biradical intermediates. More importantly, intramolecular hydrogen bonds seem to give an additional effect on conformational control of the biradical reactivity.

AZOLYLMETHYLENEHYDRAZINE DERIVATIVE AND USE THEREOF

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Page/Page column 33, (2010/04/25)

An azolylmethylidenehydrazine derivative represented by the formula (I) wherein Ar is an aryl group optionally having substituent(s), a heteroaryl group optionally having substituent(s) or a heteroaryl group optionally having substituent(s), R1

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