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Boronic acid, (5-hydroxy-2-naphthalenyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

590417-28-0

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590417-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 590417-28-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,0,4,1 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 590417-28:
(8*5)+(7*9)+(6*0)+(5*4)+(4*1)+(3*7)+(2*2)+(1*8)=160
160 % 10 = 0
So 590417-28-0 is a valid CAS Registry Number.

590417-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-hydroxynaphthalen-2-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 5-hydroxy-2-naphthaleneboronic 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:590417-28-0 SDS

590417-28-0Relevant articles and documents

Singlet oxygen carrier for inhibiting beta-amyloid protein aggregation as well as preparation method and application thereof

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Paragraph 0074-0076; 0078-0079; 0089-0092, (2021/11/27)

The invention discloses a singlet oxygen carrier for inhibiting beta-amyloid protein aggregation as well as a preparation method and application thereof, which belongs to the technical field of biological medicines. The singlet oxygen carrier for inhibiting beta-amyloid protein aggregation contains two functional groups, namely a benzothiazole group and a singlet oxygen carrier. The benzothiazole group can be selectively combined with the beta-amyloid protein, so that the targeting property of the system is improved, the aggregation of the beta-amyloid protein is inhibited, and the neurotoxicity caused by the beta-amyloid protein is reduced. The endoperoxide in the system can release singlet oxygen under a certain condition, and the singlet oxygen can oxidize the beta-amyloid protein, so that the aggregation of the beta-amyloid protein is further limited, and the toxicity is reduced. The carrier has dual inhibition effects on beta-amyloid protein, and has application potentials of treating related diseases caused by beta-amyloid protein aggregation and relieving Alzheimer's disease and other diseases.

Substituted phenylalkanoic acid derivatives and use thereof

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Page 61-62, (2008/06/13)

A compound represented by the formula (I) or a salt thereof: wherein n represents an integer of 1 to 3, R represents an alkyl group having 3 to 8 carbon atoms, a group represented by the following formula: R1(CH2)k— (wherein k represents 0 or an integer of 1 to 3; R1 represents a saturated cyclic alkyl group having 3 to 7 carbon atoms or a saturated condensed cyclic alkyl group having 6 to 8 carbon atoms, and the group R1 may be substituted with a lower alkyl group having 1 to 4 carbon atoms) and the like, and Ar represents a condensed bicyclic group such as naphthalen-1-yl group, which has suppressing action on prostaglandin and leukotriene production and is useful for prophylactic and/or therapeutic treatment of various inflammatory diseases and the like caused by these lipid mediators.

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