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Octyl (R)-2-(4-chloro-2-methylphenoxy)propionate is a chemical compound that belongs to the class of aryloxyphenoxypropionate herbicides. It is commonly used in agricultural and commercial settings for its weed control properties, exhibiting selective action on specific types of plants while leaving others unharmed.

66423-13-0

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66423-13-0 Usage

Uses

Used in Agricultural Industry:
Octyl (R)-2-(4-chloro-2-methylphenoxy)propionate is used as a herbicide for controlling weeds and unwanted vegetation in a variety of crops. It is particularly effective in crops such as soybeans, corn, and cotton, where it inhibits the growth of target plants without causing harm to the desired crops.
Used in Commercial Settings:
In commercial settings, Octyl (R)-2-(4-chloro-2-methylphenoxy)propionate is used as a herbicide to manage unwanted vegetation in areas such as lawns, gardens, and other landscaped areas. Its selective nature allows for effective weed control without causing damage to the surrounding plants.

Check Digit Verification of cas no

The CAS Registry Mumber 66423-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,2 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66423-13:
(7*6)+(6*6)+(5*4)+(4*2)+(3*3)+(2*1)+(1*3)=120
120 % 10 = 0
So 66423-13-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H27ClO3/c1-4-5-6-7-8-9-12-21-18(20)15(3)22-17-11-10-16(19)13-14(17)2/h10-11,13,15H,4-9,12H2,1-3H3/t15-/m1/s1

66423-13-0SDS

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 octyl (2R)-2-(4-chloro-2-methylphenoxy)propanoate

1.2 Other means of identification

Product number -
Other names EINECS 266-358-7

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:66423-13-0 SDS

66423-13-0Downstream Products

66423-13-0Relevant academic research and scientific papers

Industrial production improvement process for (R)-2-(4-chlorine-2-methyl phenoxy) octyl propionate root retarder

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, (2018/11/22)

The invention discloses an industrial production improvement process for a (R)-2-(4-chlorine-2-methyl phenoxy) octyl propionate root retarder which can be used as a root retarder. The production process is characterized by comprising the following steps: by taking methylbenzene as a solvent, triethylamine as an acid-binding agent, and pyridine as a catalyst, carrying out sulfonation on L-ethyl lactate and paratoluensulfonyl chloride so as to obtain a corresponding sulfonyl ester intermediate product; under the promotion of sodium hydroxide, carrying out etherification on the sulfonyl ester intermediate product with 4-chlorine o-cresol so as to obtain an aromatic ester ether compound; at a certain temperature and pressure, carrying out ester exchange on the ester ether compound with n-octylalcohol, thereby obtaining the (R)-2-(4-chlorine-2-methyl phenoxy) octyl propionate. The (R)-2-(4-chlorine-2-methyl phenoxy) octyl propionate prepared by using the production improvement process disclosed by the invention is high in optical content, small in raw material optical loss and high in yield, and can be directly applied to process production of root puncturing resistant waterproof rolls. The production process has large application prospects.

Preparation method of octyl (R)-2-(4-chloro-2-methylphenoxy) propionate root retarder

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, (2018/04/01)

The invention discloses a preparation method of octyl (R)-2-(4-chloro-2-methylphenoxy) propionate which can be used as a root retarder. The preparation method comprises the following steps: with ethyl L-lactate as a raw material, sulfonating together with p-toluenesulfonyl chloride to obtain a corresponding sulfonyl ester compound; etherifying the sulfonyl ester compound and 4-chloro-o-cresol to obtain a corresponding aromatic ether ester compound; and finally, performing transesterification on the ether ester compound and n-octyl alcohol to obtain octyl (R)-2-(4-chloro-2-methylphenoxy) propionate. Octyl (R)-2-(4-chloro-2-methylphenoxy) propionate prepared by the preparation method provided by the invention is high in optical content, relatively small in optical loss of raw materials and relatively high in yield. The invention establishes a reaction system with the characteristics of simple preparation process, mild reaction condition and low cost, so that the problems that the compound is imported and has a scarce source are solved to a certain extent.

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