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33441-56-4

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33441-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33441-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,4 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 33441-56:
(7*3)+(6*3)+(5*4)+(4*4)+(3*1)+(2*5)+(1*6)=94
94 % 10 = 4
So 33441-56-4 is a valid CAS Registry Number.

33441-56-4SDS

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 2-ethoxythiobenzate

1.2 Other means of identification

Product number -
Other names Ethyl 2-mercaptobenzoate

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:33441-56-4 SDS

33441-56-4Relevant articles and documents

Synthesis and biological evaluation of sulfur-containing cinnamate and salicylate derivatives

Chiang, Chih-Chia,Chang, Tsu-Chung,Tsai, Hou-Jen,Hsu, Ling-Yih

, p. 369 - 373 (2008/09/20)

UV irradiation induced formation of reactive oxygen radical species and matrix metalloproteinases (MMPs) are thought to be involved in photo-damage to the skin. MMP-1 is the major collagenolytic enzyme responsible for collagen destruction in skin tissue. To develop new anti-photoaging agents, a series of 2,2′-dithiocinnamate derivatives and 2,2′-dithio or 2-thiobenzoate derivatives were designed and synthesized. The biological activities of the synthesized compounds were assayed for ABTS [2,2′-azinobis-(3-ethyl-benzo- thiazoline-6-sulfonic acid)] radical scavenging activity, MMP-1 inhibitory activity, and cytotoxicity to human dermal fibroblast cells. Compounds with potential of resistance to UV irradiation were identified. These compounds are expected to be useful for preventing photo-damage to the skin.

New macrocyclic ligands. XIV: Synthesis and X-ray structures of potentially pentadentate ligands incorporating non-symmetrically arranged N4S-, N3OS-, N2O2S- and N2S2O-heteroatoms

Baldwin, Darren S.,Bowden, Bruce F.,Duckworth, Paul A.,Lindoy, Leonard F.,McCool, Brian J.,Meehan, George V.,Vasilescu, Ioana M.,Wild, S. Bruce

, p. 597 - 603 (2007/10/03)

The synthesis and characterization of new mixed-donor macrocyclic ligands incorporating nitrogen, sulfur and/or oxygen heteroatoms are described. The new 17- or 18-membered macrocyclic rings contain unsymmetrical arrangements of their heteroatoms in contr

No-donors, part 3: Nitrooxyacylated thiosalicylates and salicylates - Synthesis and biological activities

Endres, Stefan,Hacker, Andreas,Noack, Eike,Kojda, Georg,Lehmann, Jochen

, p. 895 - 901 (2007/10/03)

Organic nitrates release nitric oxide when incubated with thiosalicylic acid. S-Nitrooxyacylated esters and amides of thiosalicylic acid, together with the corresponding salicylates, were synthesized in order to perform a first in vitro evaluation of these new nitrate-thiol-hybrid prodrugs. These prodrugs might release NO in vivo after biotransformation without the use of endogenous reductives. None of these prodrugs released NO spontaneously when dissolved in buffer solution, but they did activate soluble guanylyl cyclase and induced vasodilatation of phenylephrine-pretreated male Wistar rat aorta in a potency range between that of isosorbiddinitrate and glycerole trinitrate.

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