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1918-18-9

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  • Carbamic acid,N-(3,4-dichlorophenyl)-, methyl ester Manufacturer CAS NO.1918-18-9 CAS NO.1918-18-9

    Cas No: 1918-18-9

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1918-18-9 Usage

Chemical Properties

Crystals. Insoluble in water and kerosene; soluble in acetone and dimethylformamide.

Uses

Herbicide.

Hazard

Toxic by ingestion.

Check Digit Verification of cas no

The CAS Registry Mumber 1918-18-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1918-18:
(6*1)+(5*9)+(4*1)+(3*8)+(2*1)+(1*8)=89
89 % 10 = 9
So 1918-18-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H7Cl2NO2/c1-13-8(12)11-5-2-3-6(9)7(10)4-5/h2-4H,1H3,(H,11,12)

1918-18-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name swep

1.2 Other means of identification

Product number -
Other names Methyl 3,4-dichlorocarbanilate

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:1918-18-9 SDS

1918-18-9Relevant articles and documents

Anti-methicillin resistant staphylococcus aureus compound and its medical use

-

Paragraph 0075-0078, (2021/02/02)

The present invention relates to a compound represented by chemical formula 1 having an antibacterial effect against Staphylococcus aureus, particularly Staphylococcus aureus resistant to existing antibacterial agents such as methicillin or the like, and to a medicinal use of the compound.

Triazolecarboxamide herbicides

-

, (2008/06/13)

Compounds of the formula: STR1 wherein X is O or S; R and R1 are substituted or unsubstituted alkyl, alkenyl, alkynyl or cycloalkyl or R and R1 may be joined to form a heterocyclic ring; R2 is substituted or unsubstituted cycloalkyl; and n is 0, 1 or 2 are disclosed as well as their postemergence and preemergence selective herbicide use against both monocot and dicot weeds in crops such as sugarbeets, cotton, soybeans and rice.

Process for the preparation of N,O-disubstituted urethanes suitable as a starting material for the preparation of isocyanates

-

, (2008/06/13)

A process for the preparation of N,O-disubstituted urethanes. Primary amines and alcohols are reacted with organic compounds having carbonyl groups at 120° to 350° C. Suitable carbonyl-containing compounds include N-unsubstituted urethanes. N-mono-substituted, N,N'-disubstituted ureas, or polyureas may be used in combination with the N-unsubstituted urethane. The product urethanes are particularly suitable for the preparation of isocyanates.

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