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816-39-7

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816-39-7 Usage

Chemical Properties

YELLOW TO DARK BROWN LIQUID

Uses

1,3-Dibromoacetone is used as an antibiotic and antimicrobial agent.

Check Digit Verification of cas no

The CAS Registry Mumber 816-39-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 816-39:
(5*8)+(4*1)+(3*6)+(2*3)+(1*9)=77
77 % 10 = 7
So 816-39-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H4Br2O/c1-2(6)3(4)5/h3H,1H3

816-39-7 Well-known Company Product Price

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  • CAS number
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  • Alfa Aesar

  • (H37325)  1,3-Dibromoacetone, 98%   

  • 816-39-7

  • 1g

  • 549.0CNY

  • Detail
  • Alfa Aesar

  • (H37325)  1,3-Dibromoacetone, 98%   

  • 816-39-7

  • 5g

  • 1717.0CNY

  • Detail
  • Alfa Aesar

  • (H37325)  1,3-Dibromoacetone, 98%   

  • 816-39-7

  • 25g

  • 5368.0CNY

  • Detail

816-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Dibromoacetone

1.2 Other means of identification

Product number -
Other names 2-Propanone, 1,3-dibromo-

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:816-39-7 SDS

816-39-7Relevant articles and documents

Two New Amphiphilic Catalysts for Ester Hydrolysis

Menger, F. M.,Persichetti, R. A.

, p. 3451 - 3452 (1987)

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Synthesis of α,β-unsaturated epoxy ketones utilizing a bifunctional sulfonium/phosphonium ylide

Eskandari, Roozbeh,Hess, Jeremy P.,Tochtrop, Gregory P.

supporting information, p. 7136 - 7139 (2021/07/28)

Herein, a new protocol for rapid synthesis of α,β-unsaturated epoxy ketones utilizing a bifunctional sulfonium/phosphonium ylide is described. This approach comprises two sequential chemoselective reactions between sulfonium and phosphonium ylides and two distinct aldehydes, which allows for the rapid construction of a variety of unsymmetric α,β-unsaturated epoxy ketones. This methodology allows the rapid construction of the core reactive functionality of a family of lipid peroxidation products, the epoxyketooctadecenoic acids, but can be further broadly utilized as a useful synthon for the synthesis of natural products, particularly those derived from oxidized fatty acids. Accordingly, a protocol utilizing this approach to synthesize the epoxyketooctadecenoic acid family of molecules is described.

Cyclopenta[d]pyrimidines And Substituted Cyclopenta[d]pyrimidines As Antitubulin and Microtubule Targeting Agents, Monocyclic Pyrimidines As Tubulin Inhibitors, And Pyrrolopyrimidines As Targeted Antifolates And Tubulin and Multiple Receptor Tyrosine Kinase Inhibition And Antitumor Agents

-

, (2016/11/09)

The present invention provides a compound of Formula I, and salts thereof, and a pharmaceutical composition comprising a compound of Formula I: wherein R1 is selected from the group consisting of and R2 is an alkyl group having from one to ten carbon atoms, or wherein R2 is selected from the group consisting of R1 is an alkyl group having from one to ten carbon atoms; and R is H, or an alkyl group having from one to ten carbon atoms, and R3 is H, an alkyl group having from one to ten carbon atoms, or a halogen. Preferably the compound of Formula V includes wherein R3 is a halogen, and most preferably wherein the halogen is chlorine. Methods of treating a patient with cancer with these compounds are also provided.

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