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13558-70-8

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13558-70-8 Usage

General Description

Methyl chloroacetylcarbamate is a chemical compound that is used primarily as a pesticide and herbicide. It is an effective inhibitor of the enzyme acetylcholinesterase, which is important for nerve function in both insects and plants. This mechanism of action makes it a potent insecticide and herbicide, as it disrupts the nervous system of target organisms. Methyl chloroacetylcarbamate is also considered to be relatively safe for use in agriculture and is widely used in the production of various crops. However, it is important to handle and apply this chemical with caution, as it can be toxic to humans and other non-target organisms if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 13558-70-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,5 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13558-70:
(7*1)+(6*3)+(5*5)+(4*5)+(3*8)+(2*7)+(1*0)=108
108 % 10 = 8
So 13558-70-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H6ClNO3/c1-9-4(8)6-3(7)2-5/h2H2,1H3,(H,6,7,8)

13558-70-8SDS

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 Methyl (2-chloroacetyl)carbamate

1.2 Other means of identification

Product number -
Other names Methyl N-(2-chloroacetyl)carbamate

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:13558-70-8 SDS

13558-70-8Relevant articles and documents

A concise approach to n-substituted rhodanines through a base-assisted one-pot coupling and cyclization process

Huo, Zhipeng,Liang, Yongxi,Sun, Xun,Tang, Mei-Lin,Zhang, Chenchen

, (2020/03/17)

An efficient approach to obtain functionalized rhodanines was developed through a base-assisted one-pot coupling and continuous cyclization of a primary amine, carbon disulfide, and methyl (2-chloroacetyl)carbamate. This conversion tolerates a broad range of functional groups and can be used to scale the preparation of N-substituted rhodanines in excellent yields.

Methyl 6-(phenylsulfinyl)imidazo[1,2-a]pyridine-2-carbamate, a potent, new anthelmintic

Bochis,Dybas,Eskola,Kulsa,Linn,Lusi,Meitzner,Milkowski,Mrozik,Olen,Peterson,Tolman,Wagner,Waksmunski,Egerton,Ostlind

, p. 235 - 237 (2007/10/04)

A series of methyl imidazo[1,2-a]pyridine-2-carbamates was synthesized for anthelmintic testing. The preparation of this class of compounds was simplified by utilization of a novel one-step condensation of the appropriately substituted 2-aminopyridine with methyl chloroacetylcarbamate. The most potent compound, methyl 6-(phenylsulfinyl) imidazo[1,2-a] pyridine-2-carbamate, was orally effective against a broad range of helminths in sheep and cattle, at a dosage of 2.5 mg/kg. Limited trials in swine and dogs demonstrated anthelmintic activity at higher dosages. Limited observations in sheep and cattle indicated that, in both species, a single oral dose of 200 mg/kg was well tolerated.

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