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15114-43-9

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15114-43-9 Usage

Chemical Properties

Light yellow to white powder

Uses

Dibromoisocyanuric acid is a bromine compound with a superior bactericidal activity.

Check Digit Verification of cas no

The CAS Registry Mumber 15114-43-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,1 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15114-43:
(7*1)+(6*5)+(5*1)+(4*1)+(3*4)+(2*4)+(1*3)=69
69 % 10 = 9
So 15114-43-9 is a valid CAS Registry Number.
InChI:InChI=1/C3HBr2N3O3/c4-7-1(9)6-2(10)8(5)3(7)11/h(H,6,9,10)

15114-43-9 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Detail
  • TCI America

  • (D3753)  Dibromoisocyanuric Acid  >97.0%(T)

  • 15114-43-9

  • 5g

  • 540.00CNY

  • Detail
  • TCI America

  • (D3753)  Dibromoisocyanuric Acid  >97.0%(T)

  • 15114-43-9

  • 25g

  • 1,700.00CNY

  • Detail
  • Aldrich

  • (737135)  Dibromoisocyanuric acid  96%

  • 15114-43-9

  • 737135-1G

  • 191.88CNY

  • Detail
  • Aldrich

  • (737135)  Dibromoisocyanuric acid  96%

  • 15114-43-9

  • 737135-5G

  • 513.63CNY

  • Detail

15114-43-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dibromo-1,3,5-triazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names DibroMoisocyanuric 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:15114-43-9 SDS

15114-43-9Relevant articles and documents

Primary amides. A general nitrogen source for catalytic asymmetric aminohydroxylation of olefins

Demko, Zachary P.,Bartsch, Michael,Sharpless, K. Barry

, p. 2221 - 2223 (2000)

(equation presented) N-Bromo,N-lithio salts of primary carboxamides have been shown to be efficient nitrogen sources for catalytic asymmetric aminohydroxylation of olefins, behaving much like the parent N-bromoacetamide in these reactions. α-Chloro-N-brom

Synthesis of tetraalkyl naphthalene bisanhydride and its model condensations with amines

Xiong, Kai,Xiao, Yi

supporting information, p. 3171 - 3175 (2013/06/27)

To improve the solubility of naphthalene bisanhydride (NTCA), four alkyl groups are incorporated to the naphthalene core via a five-step procedure. The new naphthalene bisanhydride derivative (TO-NTCA) shows much higher reactivity than the parent NTCA in the model condensations with ortho-diaminobenzene and 2-ethylhexylamine and gives corresponding soluble molecules with excellent yields. Hence, TO-NTCA is a potential monomer for condensations.

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