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(2-methyl-5-phenylfuran-3,4-diyl)dimethanediyl bis(methylcarbamate) is a carbamate compound characterized by a furan ring with a methyl and phenyl group, connected by a dimethanediyl bridge and capped with two methylcarbamate groups. This unique molecular structure endows it with specific biological activities and applications.

92126-06-2

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92126-06-2 Usage

Uses

Used in Pesticide Industry:
(2-methyl-5-phenylfuran-3,4-diyl)dimethanediyl bis(methylcarbamate) is used as an insecticide for its ability to inhibit acetylcholinesterase, an enzyme crucial for nerve function in insects. This inhibition disrupts the nervous system of pests, leading to their eventual death, thereby providing effective pest control in agricultural settings.
Used in Agricultural Applications:
In the agricultural sector, (2-methyl-5-phenylfuran-3,4-diyl)dimethanediyl bis(methylcarbamate) serves as a critical tool for protecting crops from insect damage. Its application helps maintain crop yields and quality by reducing the impact of pests, which is essential for ensuring food security and sustainable farming practices.

Check Digit Verification of cas no

The CAS Registry Mumber 92126-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,2 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92126-06:
(7*9)+(6*2)+(5*1)+(4*2)+(3*6)+(2*0)+(1*6)=112
112 % 10 = 2
So 92126-06-2 is a valid CAS Registry Number.

92126-06-2SDS

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 [2-methyl-4-(methylcarbamoyloxymethyl)-5-phenylfuran-3-yl]methyl N-methylcarbamate

1.2 Other means of identification

Product number -
Other names 2-methyl-3,4-bis(hydroxymethyl)-5-phenylfuran bis(methylcarbamate)

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:92126-06-2 SDS

92126-06-2Downstream Products

92126-06-2Relevant academic research and scientific papers

Synthesis and evaluation of furan, thiophene, and azole bis[(carbamoyloxy)methyl] derivatives as potential antineoplastic agents

Anderson,Jones

, p. 1559 - 1565 (2007/10/02)

A series of bis(hydroxymethyl)-substituted heterocycles were synthesized and converted to the corresponding bis(methylcarbamate) derivatives. The heterocyclic systems studied were based on 2-phenyl-3-methylfuran, 1-phenylpyrazole, 1-phenyl-5-methylpyrazole, 1-phenyl-5-methylthiopene, 1-phenyl-1,2,3-triazole, 3-phenylisoxazole, 3-phenylisothiazole, 2-phenylthiazole, and 2-phenyloxazole. None of the bis(carbamates) prepared was active against murine P388 lymphocytic leukemia. Pyrrole bis(carbamate), which exhibited antileukemic activity, also showed reactivity toward 4-(p-nitrobenzyl)pyridine while the inactive bis(carbamates) were unreactive in the 4-(p-nitrobenzyl)pyridine assay.

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