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2905-65-9

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2905-65-9 Usage

Description

Methyl 3-chlorobenzoate is an organic compound with the chemical formula C8H7ClO2. It is a clear, colorless to yellow liquid that has been studied for its resonance-enhanced multiphoton ionization (REMPI) spectrum and fluorescence excitation spectrum in a supersonic free jet. Methyl 3-chlorobenzoate has also been investigated for its reaction with lithium diisobutyl-t-butoxyaluminum hydride (LDBBA).

Uses

Used in Chemical Synthesis:
Methyl 3-chlorobenzoate is used as an intermediate in the synthesis of various organic compounds, particularly those involving the benzene ring. Its reactivity and functional groups make it a versatile building block for creating a wide range of chemical products.
Used in Pharmaceutical Industry:
Methyl 3-chlorobenzoate is used as a starting material for the synthesis of pharmaceutical compounds. Its unique structure and reactivity allow for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
Methyl 3-chlorobenzoate is used as a precursor in the development of agrochemicals, such as pesticides and herbicides. Its chemical properties make it suitable for creating compounds that can effectively control pests and weeds in agricultural settings.
Used in Dye and Pigment Industry:
Methyl 3-chlorobenzoate is used as a raw material in the production of dyes and pigments. Its chemical structure contributes to the color and stability of these products, making it an important component in the manufacturing process.
Used in Flavor and Fragrance Industry:
Methyl 3-chlorobenzoate is used as a component in the creation of flavors and fragrances. Its unique chemical properties can contribute to the development of new and complex scents for various applications, such as perfumes, candles, and air fresheners.
Used in Research and Development:
Methyl 3-chlorobenzoate is used as a research compound for studying various chemical reactions and processes. Its unique properties make it an interesting subject for scientists to explore and understand, potentially leading to new discoveries and applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 2905-65-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,0 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2905-65:
(6*2)+(5*9)+(4*0)+(3*5)+(2*6)+(1*5)=89
89 % 10 = 9
So 2905-65-9 is a valid CAS Registry Number.

2905-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-chlorobenzoate

1.2 Other means of identification

Product number -
Other names Benzoic acid,3-chloro-,methyl ester

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:2905-65-9 SDS

2905-65-9Relevant articles and documents

Ultrafine Copper Oxide Particles Dispersed on Nitrogen-Doped Hollow Carbon Nanospheres for Oxidative Esterification of Biomass-Derived 5-Hydroxymethylfurfural

Gupta, Shyam Sunder R.,Vinu, Ajayan,Kantam, Mannepalli Lakshmi

, p. 259 - 269 (2021)

One-pot synthesis of furan-2,5-dimethylcarboxylate (FDMC) from 5-hydroxymethylfurfural (HMF) is highly demanding for the commercial production of polyethylene furanoate (PEF). Herein, a direct synthesis of FDMC is reported from oxidative esterification of HMF using ultrafine CuO particles dispersed on nitrogen-doped hollow carbon nanospheres (CuO/N?C?HNSs) as a catalyst and tert-butyl hydroperoxide (TBHP) as an oxidizing and methylating reagent. The CuO/N?C?HNSs was prepared through a template protection-sacrifice strategy using SiO2 as a sacrificial template and histidine as the precursor for N and C. N-doping facilitated a strong interaction between the support and copper species, affording formation of CuO nanoparticles of less than 10 nm in size. By virtue of the highly dispersed CuO nanoparticles and a high BET surface area 373 m2/g, the CuO/N?C?HNSsshows excellent catalytic performance in the selective conversion of HMF into FDMC affording 93 % yield of the desired product with a TON value of 49. Furthermore, the oxidative esterification involving SP3C?H bond functionalization is also demonstrated using the same catalyst.

Antibacterial and Antiviral Activities of 1,3,4-Oxadiazole Thioether 4H-Chromen-4-one Derivatives

Cao, Xiao,Liu, Fang,Liu, Liwei,Liu, Tingting,Peng, Feng,Wang, Qifan,Xie, Chengwei,Xue, Wei,Yang, Jinsong

, p. 11085 - 11094 (2021/10/01)

Various 1,3,4-oxadiazole thioether 4H-chromen-4-one derivatives were conceived. The title compounds demonstrated striking inhibitory effects againstXac,Psa, andXoo. EC50data exhibited that A8 (19.7 μg/mL) had better antibacterial activity againstXoothan myricetin, BT, and TC. Simultaneously, the mechanism of action of A8 had been verified by SEM. The results of anti-tobacco mosaic virus indicated that A9 had the bestin vivoantiviral effect compared with ningnanmycin. From the data of MST, it could be seen that A9 (0.003 ± 0.001 μmol/L) exhibited a strong binding capacity, which was far superior to ningnanmycin (2.726 ± 1.301 μmol/L). This study shows that the 1,3,4-oxadiazole thioether 4H-chromen-4-one derivatives may become agricultural drugs with great potential.

Convenient synthesis of benziodazolone: New reagents for direct esterification of alcohols and amidation of amines

Postnikov, Pavel S.,Rohde, Gregory T.,Saito, Akio,Shea, Michael T.,Vlasenko, Yulia A.,Yoshimura, Akira,Yusubov, Mekhman S.,Zhdankin, Viktor V.

, (2021/12/17)

Hypervalent iodine heterocycles represent one of the important classes of hypervalent iodine reagents with many applications in organic synthesis. This paper reports a simple and convenient synthesis of benziodazolones by the reaction of readily available iodobenzamides with m-chloroperoxybenzoic acid in acetonitrile at room temperature. The structure of one of these new iodine heterocycles was confirmed by X-ray analysis. In combination with PPh3 and pyridine, these benziodazolones can smoothly react with alcohols or amines to produce the corresponding esters or amides of 3-chlorobenzoic acid, respectively. It was found that the novel benziodazolone reagent reacts more efficiently than the analogous benziodoxolone reagent in this esterification.

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