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1746-81-2

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1746-81-2 Usage

Safety Profile

Moderately toxic by ingestion. Experimental teratogenic and reproductive effects. When heated to decomposition it emits very toxic fumes of Cland NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 1746-81-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,4 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1746-81:
(6*1)+(5*7)+(4*4)+(3*6)+(2*8)+(1*1)=92
92 % 10 = 2
So 1746-81-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H11ClN2O2/c1-12(14-2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)

1746-81-2SDS

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 monolinuron

1.2 Other means of identification

Product number -
Other names N’-(4-chlorophenyl)-N-methoxy-N-methylurea

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:1746-81-2 SDS

1746-81-2Downstream Products

1746-81-2Relevant articles and documents

Preparation method of monolinuron

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Paragraph 0040-0075, (2019/04/02)

The invention belongs to the field of pesticide synthesis technology, and particularly relates to a preparation method of monolinuron. A monolinuron product is prepared through a one-step reaction ina polar solvent by analyzing the structure of monolinuron and the steric hindrance of chemical synthesis, and using cheap and easily available p-chlorophenyl isocyanate and dimethylhydroxylamine hydrochloride as main raw materials. The product purity reaches 98% or more than 98%, and the product yield is close to 80%, therefore, the technical problems of complicated process, multiple by-products and environmental pollution existing in the preparation technology of monolinuron in the prior art are solved.

Herbicidal composition for upland farming and weeding method

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, (2008/06/13)

A herbicidal composition for upland farming which can control weeds that have been difficult to control, for example, cleavers, chickweed, birdseye speedwell and violet, said composition containing as active ingredients a 3-substituted phenylpyrazole derivative represented by the general formula (I): STR1 (wherein R is a hydrogen atom, a C1-6 alkyl group, a C3-6 cycloalkyl group, a C1-6 haloalkyl group, a C2-6 alkenyl group or a C2-6 alkynyl group, R1 is a C1-6 alkyl group, X1 and X2, which may be the same or different, are halogen atoms, and Y is an oxygen atom or a sulfur atom) and at least one compound selected from the group consisting of sulfonylurea derivatives, phenylurea derivatives and phenoxy fatty acid derivatives; and a weeding method using said composition.

Composition for defoliating plants

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, (2008/06/13)

New compositions for defoliating plants possessed of synergistic activity comprising (A) a compound of formula I STR1 in which R1 is hydrogen or C1 -C4 -alkyl, R2 is hydrogen, C1 -C4 -alkyl, C1 -C4 -alkoxy or C1 -C4 -alkylthio, R3 is hydrogen, C1 -C4 -alkyl, C1 -C4 -alkoxy, C1 -C4 -alkylthio or C3 -C8 -cycloalkyl, wherein R2 and R3 taken together with the nitrogen atom to which they are attached is a morpholino- piperidino- or pyrrolidino-group, X is oxygen or sulfur, Y can be the same or different and is hydrogen, halogen, C1 -C4 -alkyl, C1 -C4 -alkoxy, C1 -C4 -alkoxy-C1 -C2 -alkyl, C1 -C4 -alkylthio, trifluoromethyl or nitro, and n is the number 1, 2, 3, 4 or 5, in combination with (B) a defoliant for plants in a proportion of 1 to 99 parts by weight of component (A) to 99 to 1 parts by weight of component (B). As the defoliant there can be employed 1,2,3-thiadiazole-5-yl-urea derivatives, 1,2,3-thiadiazole-5-carboxylic acid derivatives, benzylaminopurine derivatives, 2,3-dihydro-5,6-dimethyl-1,4-dithiine-1,1,4,4-tetroxide, 1,1'-dimethyl-4,4'-bipyridilium-dichloride, sodium chlorate and S,S,S-tributylphosphortrithioate. The compositions of the invention are especially suitable for use in the defoliation of cotton plants.

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