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51329-15-8

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51329-15-8 Usage

General Description

Methyl 3,5-dibromobenzoate is a chemical compound with the molecular formula C9H7Br2O2. It is a benzene derivative, specifically a derivative of benzoic acid, with two bromine atoms attached to the benzene ring at the 3 and 5 positions. METHYL 3,5-DIBROMOBENZOATE is commonly used in organic synthesis and chemical research as a building block for the synthesis of more complex molecules. It is also used as an intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Methyl 3,5-dibromobenzoate is a colorless to pale yellow liquid with a slightly sweet odor and is flammable, requiring proper handling and storage.

Check Digit Verification of cas no

The CAS Registry Mumber 51329-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,2 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51329-15:
(7*5)+(6*1)+(5*3)+(4*2)+(3*9)+(2*1)+(1*5)=98
98 % 10 = 8
So 51329-15-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H6Br2O2/c1-12-8(11)5-2-6(9)4-7(10)3-5/h2-4H,1H3

51329-15-8 Well-known Company Product Price

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  • TCI America

  • (M1929)  Methyl 3,5-Dibromobenzoate  >98.0%(GC)

  • 51329-15-8

  • 5g

  • 690.00CNY

  • Detail
  • TCI America

  • (M1929)  Methyl 3,5-Dibromobenzoate  >98.0%(GC)

  • 51329-15-8

  • 25g

  • 2,450.00CNY

  • Detail
  • Alfa Aesar

  • (B20668)  Methyl 3,5-dibromobenzoate, 98%   

  • 51329-15-8

  • 1g

  • 372.0CNY

  • Detail
  • Alfa Aesar

  • (B20668)  Methyl 3,5-dibromobenzoate, 98%   

  • 51329-15-8

  • 5g

  • 1441.0CNY

  • Detail

51329-15-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3,5-dibromobenzoate

1.2 Other means of identification

Product number -
Other names Methyl3,5-dibromobenzoate

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:51329-15-8 SDS

51329-15-8Relevant articles and documents

Natural gas purification using a porous coordination polymer with water and chemical stability

Duan, Jingui,Jin, Wanqin,Krishna, Rajamani

, p. 4279 - 4284 (2015)

Porous coordination polymers (PCPs), constructed by bridging the metals or clusters and organic linkers, can provide a functional pore environment for gas storage and separation. But the rational design for identifying PCPs with high efficiency and low energy cost remains a challenge. Here, we demonstrate a new PCP, [(Cu4Cl)(BTBA)8·(CH3)2NH2)·(H2O)12]·xGuest (PCP-33?guest), which shows high potential for purification of natural gas, separation of C2H2/CO2 mixtures, and selective removal of C2H2 from C2H2/C2H4 mixtures at ambient temperature. The lower binding energy of the framework toward these light hydrocarbons indicates the reduced net costs for material regeneration, and meanwhile, the good water and chemical stability of it, in particular at pH = 2 and 60 °C, shows high potential usage under some harsh conditions. In addition, the adsorption process and effective site for separation was unravelled by in situ infrared spectroscopy studies.

Optimizing Multivariate Metal-Organic Frameworks for Efficient C2H2/CO2Separation

Fan, Weidong,Yuan, Shuai,Wang, Wenjing,Feng, Liang,Liu, Xiuping,Zhang, Xiurong,Wang, Xia,Kang, Zixi,Dai, Fangna,Yuan, Daqiang,Sun, Daofeng,Zhou, Hong-Cai

supporting information, p. 8728 - 8737 (2020/12/25)

Adsorptive separation of acetylene (C2H2) from carbon dioxide (CO2) promises a practical way to produce high-purity C2H2 required for industrial applications. However, challenges exist in the pore environment engineering of porous materials to recognize two molecules due to their similar molecular sizes and physical properties. Herein, we report a strategy to optimize pore environments of multivariate metal-organic frameworks (MOFs) for efficient C2H2/CO2 separation by tuning metal components, functionalized linkers, and terminal ligands. The optimized material UPC-200(Al)-F-BIM, constructed from Al3+ clusters, fluorine-functionalized organic linkers, and benzimidazole terminal ligands, demonstrated the highest separation efficiency (C2H2/CO2 uptake ratio of 2.6) and highest C2H2 productivity among UPC-200 systems. Experimental and computational studies revealed the contribution of small pore size and polar functional groups on the C2H2/CO2 selectivity and indicated the practical C2H2/CO2 separation of UPC-200(Al)-F-BIM.

Comparison of Phenylacetates with Benzoates and Phenylpropanoates as Antifeedants for the Pine Weevil, Hylobius abietis

Unelius, C. Rikard,Bohman, Bj?rn,Nordlander, G?ran

, p. 11797 - 11805 (2018/11/21)

This study concludes an extensive investigation of antifeedants for the pine weevil, Hylobius abietis (Coleoptera: Curculionidae), an economically important pest of planted conifer seedlings. Building on the previously reported antifeedant effects of benzoates and phenylpropanoids (aromatic compounds with one- or three-carbon-atom substituents on the benzene ring), we here report the antifeedant effects of compounds with two-carbon-atom side chains (i.e., phenylacetates). We also present new results; the best antifeedants from the benzoate class were tested at 10-fold lower concentrations in order to find the optimal antifeedants. Generally, for all three compound classes, efficient antifeedants were found to have one or two methyl, chloro, or methoxy substituents on the aromatic ring. For monosubstituted phenylpropanoids, the substituent preferably should be in the para-position. In the search for synergistic antifeedant effects among the three compound classes, combinations of compounds from the three classes were tested in binary and ternary mixtures.

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