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125518-46-9

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125518-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125518-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,5,1 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 125518-46:
(8*1)+(7*2)+(6*5)+(5*5)+(4*1)+(3*8)+(2*4)+(1*6)=119
119 % 10 = 9
So 125518-46-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H9NO4S2/c15-11-12(19-13(16)14-11)20(17,18)10-6-5-8-3-1-2-4-9(8)7-10/h1-7,12H,(H,14,15,16)

125518-46-9SDS

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 5-naphthalen-2-ylsulfonyl-1,3-thiazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-(Naphthalene-2-sulfonyl)-thiazolidine-2,4-dione

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:125518-46-9 SDS

125518-46-9Downstream Products

125518-46-9Relevant articles and documents

ABC EXPRESSION PROMOTERS

-

, (2008/06/13)

The ABCA1 mRNA expression-promoting agent, LXRα mRNA expression-promoting agent, ABCG1 mRNA expression-promoting agent, cholesterol efflux-promoting agent, cholesteryl ester accumulation-inhibiting agent, ACAT-1 mRNA expression-inhibiting agent and CEH mRNA expression-promoting agent of the present invention are excellent in the ability to control cholesterol distribution in the body and have low toxicity.

Apoptosis inhibitor

-

, (2008/06/13)

An apoptosis inhibitor which comprises a compound of the formula: wherein R represents a hydrocarbon group that may be substituted or a heterocyclic group that may be substituted; Y represents a group of the formula: —CO—, —CH(OH)— or —NR3— where R3represents an alkyl group that may be substituted; m is 0 or 1; n is 0, 1 or 2; X represents CH or N; A represents a chemical bond or a bivalent aliphatic hydrocarbon group having 1 to 7 carbon atoms; Q represents oxygen or sulfur; R1represents hydrogen or an alkyl group; ring E may have further 1 to 4 substituents, which may form a ring in combination with R1; L and M respectively represent hydrogen or may be combined with each other to form a chemical bond; or a salt thereof, or a compound having an insulin sensitivity enhancing activity.

5-[(1- and 2-naphthalenyl) sulfonyl]-2,4-thiazolidinediones and derivatives thereof

-

, (2008/06/13)

Disclosed herein are 1- or 2-thio, thiomethylene, and sulfonylnaphthalene derivatives of formulas I and II STR1 or a pharmaceutically acceptable catonic salt thereof, wherein n is 0 or 1 R5 is hydrogen, bromo, chloro, trifluoromethyl or difluoroethyl; R6 is hydrogen, hydroxy, methoxy or ethoxy; and R7 is hydrogen or R7 and R6 are both methyl or ethyl carbonate, provided that, when S(O)2 is in the 2 position of the naphthalene ring, R5, R6 and R7 are each hydrogen. The disclosed compounds possess blood-glucose lowering actions and are useful in the treatment of diabetes mellitus.

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