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(2R)-2-(2,4-dichlorophenoxy)propanoic acid: N-methylmethanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104786-87-0 Structure
  • Basic information

    1. Product Name: (2R)-2-(2,4-dichlorophenoxy)propanoic acid: N-methylmethanamine
    2. Synonyms: (2R)-2-(2,4-dichlorophenoxy)propanoic acid: N-methylmethanamine
    3. CAS NO:104786-87-0
    4. Molecular Formula: C11H15Cl2NO3
    5. Molecular Weight: 280.1477
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104786-87-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 348.3°Cat760mmHg
    3. Flash Point: 164.5°C
    4. Appearance: /
    5. Density: g/cm3
    6. Vapor Pressure: 1.9E-05mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (2R)-2-(2,4-dichlorophenoxy)propanoic acid: N-methylmethanamine(CAS DataBase Reference)
    11. NIST Chemistry Reference: (2R)-2-(2,4-dichlorophenoxy)propanoic acid: N-methylmethanamine(104786-87-0)
    12. EPA Substance Registry System: (2R)-2-(2,4-dichlorophenoxy)propanoic acid: N-methylmethanamine(104786-87-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 104786-87-0(Hazardous Substances Data)

104786-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104786-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,8 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 104786-87:
(8*1)+(7*0)+(6*4)+(5*7)+(4*8)+(3*6)+(2*8)+(1*7)=140
140 % 10 = 0
So 104786-87-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H8Cl2O3.C2H7N/c1-5(9(12)13)14-8-3-2-6(10)4-7(8)11;1-3-2/h2-5H,1H3,(H,12,13);3H,1-2H3/t5-;/m1./s1

104786-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dichlorprop-P-dimethylammonium

1.2 Other means of identification

Product number -
Other names (2R)-2-(2,4-dichlorophenoxy)propanoic acid—N-methylmethanamine

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:104786-87-0 SDS

104786-87-0Downstream Products

104786-87-0Relevant articles and documents

Preparation method of chlorophenoxycarboxamide salt

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Paragraph 0086; 0088, (2019/01/08)

The invention provides a preparation method of chlorophenoxycarboxamide salt, wherein the preparation method includes the following steps: S1) carrying out 2-site and/or 4-site selective chlorinationreaction of phenoxycarboxylic ester with a chlorinating agent under the action of a catalyst A and a catalyst B to obtain chlorophenoxycarboxylic ester, wherein the catalyst A is Lewis acid, and the catalyst B has the following structural formula of R1'-S-R2'; and S2) carrying out ammonolysis reaction of chlorophenoxycarboxylic ester and amine to obtain chlorophenoxycarboxamide salt. By redesigning of the process route and fine screening of the catalysts and the chlorinating agent, the method reduces energy consumption, improves chlorination selectivity and avoids loss of effective components.The yield of the obtained chlorophenoxycarboxamide salt can reach 98.5% or more. At the same time, the production of high-salt wastewater is completely eradicated, the dust hazard caused by drying and use of chlorophenoxycarboxylic acid is avoided, energy is saved and equipment investment is reduced.

PROCESS FOR PREPARATION OF HERBICIDAL SALTS

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Page/Page column 8, (2011/12/04)

A process for the preparation of solid amine salts of aromatic substituted carboxylic acid herbicides by reaction of the aromatic substituted carboxylic acid herbicide with an amine comprising reacting the aromatic substituted carboxylic acid herbicide in an ether solvent with an amine to form the amine salt and collecting the amine salt of the aromatic substituted carboxylic acid herbicide as a precipitate from the ether solvent reaction mixture wherein the ether is a dialiphatic ether comprising at least one primary aliphatic group.

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