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160693-21-0

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160693-21-0 Usage

General Description

4-CHLORO-2-PHENOXYPHENYL ISOCYANATE 97 is a chemical compound with the molecular formula C13H8ClNO2. It is a highly reactive isocyanate compound that is used in the production of polyurethane materials. This chemical is known for its strong irritant properties and should be handled with extreme care. It is important to use proper safety precautions when working with 4-CHLORO-2-PHENOXYPHENYL ISOCYANATE 97, including wearing appropriate protective equipment and working in a well-ventilated area.

Check Digit Verification of cas no

The CAS Registry Mumber 160693-21-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,6,9 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 160693-21:
(8*1)+(7*6)+(6*0)+(5*6)+(4*9)+(3*3)+(2*2)+(1*1)=130
130 % 10 = 0
So 160693-21-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H8ClNO2/c14-10-6-7-12(15-9-16)13(8-10)17-11-4-2-1-3-5-11/h1-8H

160693-21-0 Well-known Company Product Price

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  • Aldrich

  • (567795)  4-Chloro-2-phenoxyphenylisocyanate  97%

  • 160693-21-0

  • 567795-1G

  • 366.21CNY

  • Detail
  • Aldrich

  • (567795)  4-Chloro-2-phenoxyphenylisocyanate  97%

  • 160693-21-0

  • 567795-5G

  • 1,289.34CNY

  • Detail
  • Aldrich

  • (567795)  4-Chloro-2-phenoxyphenylisocyanate  97%

  • 160693-21-0

  • 567795-1G

  • 366.21CNY

  • Detail
  • Aldrich

  • (567795)  4-Chloro-2-phenoxyphenylisocyanate  97%

  • 160693-21-0

  • 567795-5G

  • 1,289.34CNY

  • Detail
  • Aldrich

  • (567795)  4-Chloro-2-phenoxyphenylisocyanate  97%

  • 160693-21-0

  • 567795-1G

  • 366.21CNY

  • Detail
  • Aldrich

  • (567795)  4-Chloro-2-phenoxyphenylisocyanate  97%

  • 160693-21-0

  • 567795-5G

  • 1,289.34CNY

  • Detail
  • Aldrich

  • (567795)  4-Chloro-2-phenoxyphenylisocyanate  97%

  • 160693-21-0

  • 567795-1G

  • 366.21CNY

  • Detail
  • Aldrich

  • (567795)  4-Chloro-2-phenoxyphenylisocyanate  97%

  • 160693-21-0

  • 567795-5G

  • 1,289.34CNY

  • Detail

160693-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-1-isocyanato-2-phenoxybenzene

1.2 Other means of identification

Product number -
Other names 5-Chloro-2-isocyanatophenyl phenyl ether

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:160693-21-0 SDS

160693-21-0Downstream Products

160693-21-0Relevant articles and documents

A new class of inhibitors of secretory phospholipase A2: enolized 1,3-dioxane-4,6-dione-5-carboxamides

Breitenstein, W.,Maerki, F.,Roggo, S.,Wiesenberg, I,Pfeilschifter, J.,et al.

, p. 649 - 658 (2007/10/02)

Enolized 1,3-dioxane-4,6-dione-5-carboxamides a were identified as a new class of inhibitors of secretory phospholipase A2 from human polymorphonuclear leucocytes (h-PMN PLA2).Among the more than 30 compounds synthesized, the most potent inhibitors (IC50 0.6-10 μM) were found in the series of 2,4-disubstituted phenyl analogues of a.Compound 1a was selected for evaluation of its biological profile.This substance potently inhibited secretory PLA2s from several sources other than human PMNs, with a clear preference for group II over group I PLA2, whereas humancytosolic PLA2 and phospholipase C were not significantly affected.Inhibition of h-PMN PLA2 was calcium-dependent.In intact mammalian cells stimulated in vitro, the release of arachidonic acid and the generation of prostaglandins and leukotrienes were inhibited at concentrations compatible with inhibition of PLA2 as an underlying mechanism.In animal models in vivo (carragheenan oedema, adjuvant arthritis, pertussis pleurisy) 1a showed antiinflammatory activity, although the effect was rather weak compared with standard reference compounds. secretory human PMN phospholipase A2 / enolized 1,3-dioxane-4,6-dione-5-carboxamide inhibitors / cellular eicosanoid synthesis / in vivo antiinflammatory activity / molecular modelling / structure-activity relationship

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