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107048-59-9

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107048-59-9 Usage

General Description

2-(Bromomethyl)-alpha-(methoxymethylene)benzeneacetic acid methyl ester is a chemical compound with the molecular formula C11H11BrO3. Its structure consists of a benzene ring with a bromomethyl and a methoxymethylene group attached to it. Additionally, it contains a carboxylic acid and a methyl ester functional group. 2-(Bromomethyl)-alpha-(methoxymethylene)benzeneacetic acid methyl ester is used in organic synthesis and pharmaceutical research as it possesses potential pharmacological properties. However, due to its chemical complexity and reactivity, special care and precautions must be taken when handling and using this chemical in laboratory settings. Overall, the unique structure and potential applications of 2-(Bromomethyl)-alpha-(methoxymethylene)benzeneacetic acid methyl ester make it an important compound in the field of organic chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 107048-59-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,0,4 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 107048-59:
(8*1)+(7*0)+(6*7)+(5*0)+(4*4)+(3*8)+(2*5)+(1*9)=109
109 % 10 = 9
So 107048-59-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H13BrO3/c1-15-8-11(12(14)16-2)10-6-4-3-5-9(10)7-13/h3-6,8H,7H2,1-2H3/b11-8-

107048-59-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-[2-(bromomethyl)phenyl]-3-methoxyprop-2-enoate

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:107048-59-9 SDS

107048-59-9Downstream Products

107048-59-9Relevant articles and documents

Design, Synthesis, Antiviral Bioactivity, and Defense Mechanisms of Novel Dithioacetal Derivatives Bearing a Strobilurin Moiety

Chen, Jin,Shi, Jing,Yu, Lu,Liu, Dengyue,Gan, Xiuhai,Song, Baoan,Hu, Deyu

, p. 5335 - 5345 (2018)

A series of dithioacetal derivatives bearing a strobilurin moiety were designed and synthesized on the basis of our previous work. The antiviral activities of these compounds against Potato virus Y (PVY), Cucumber mosaic virus (CMV), and Tobacco mosaic virus (TMV) were systematically evaluated. Bioassay results indicated that C14 elicited excellent curative and protective activities against PVY, CMV, and TMV. The former had 50% effective concentrations (EC50) of 125.3, 108.9, and 181.7 μg/mL, respectively, and the latter had 148.4, 113.2, and 214.6 μg/mL, respectively, which were significantly superior to those of lead compound 6f (297.6, 259.6, and 582.4 μg/mL and 281.5, 244.3, and 546.3 μg/mL, respectively), Ningnanmycin (440.5, 549.1, and 373.8 μg/mL and 425.3, 513.3, and 242.7 μg/mL, respectively), Chitosan oligosaccharide (553.4, 582.8, and 513.8 μg/mL and 547.3, 570.6, and 507.9 μg/mL, respectively), and Ribavirin (677.4, 690.3, and 686.5 μg/mL and 652.7, 665.4, and 653.4 μg/mL, respectively). Moreover, defensive enzyme activities and RT-qPCR analysis demonstrated that the antiviral activity was associated with the changes of SOD, CAT, and POD activities in tobacco, which was proved by the related proteins of abscisic acid signaling pathway. This work provided a basis for further design, structural modification, and development of dithioacetal derivatives as new antiviral agents.

A 2 - bromo methyl of compounds of preparation method

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Paragraph 0046; 0049; 0050, (2017/12/05)

The invention discloses a method for preparing a 2-benzyl bromide compound. The method comprises the following steps: carrying out a contact reaction on a compound shown as a formula (2), an organic solvent and bromate in the presence of hydrosulphite and a catalyst, thereby obtaining a compound shown as a formula (1), wherein the structural formula is as shown in the description, and in the formula (1) and the formula (2), R1 refers to C1-C4 alkyl, R2 refers to C1-C4 alkyl, X refers to nitrogen atoms or oxygen atoms, and Z refers to CH or nitrogen atoms. According to the method for preparing the 2-benzyl bromide compound disclosed by the invention, the operation conditions are simple, the bromine utilization rate is high, corrosive gases are avoided, harm to the environment is avoided, the target product is high in selectivity and high in yield, and the method is mild in production conditions and low in production cost. Therefore, the method can be suitable for large-scale industrial production.

METHOXYACRYLATE-BASED FUNGICIDE AND METHODS FOR PREPARING AND USING THE SAME

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Page/Page column 3, (2010/12/18)

A pharmaceutical composition of fungicide including at least a compound represented by Formula (I). The pharmaceutical composition of fungicide can further include an emulsifier, a cosolvent, a stabilizer, and a solvent. The fungicide can prevent and treat powdery mildew, downy mildew, gray mold, brown spot, scab of vegetables and fruits, southern leaf blight of corn, rice false smut, citrus stem-end rot, and rape sclerotinia rot, with high efficiency, low toxicity, and relative environmental friendliness. A method of preparing the fungicide and a method of using thereof are also provided.

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