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Thifensulfuron is an N-sulfonylurea herbicide characterized by a sulfur atom attached to a 2-carboxythiophen-3-yl group and a non-sulfonated nitrogen substituted by a 4-methoxy-6-methyl-1,3,5-triazin-2-yl group. It is known for its effectiveness in controlling grass and broad-leaved weeds.
Used in Agricultural Industry:
Thifensulfuron is used as a post-emergence herbicide for the control of grass and broad-leaved weeds. It is particularly effective in targeting unwanted vegetation that emerges after crop planting, ensuring a healthy and productive crop yield.
Used in Weed Management:
Thifensulfuron is used as a selective herbicide for weed management in various crops. It helps in reducing the need for manual weeding and other labor-intensive practices, leading to more efficient and cost-effective agricultural practices.
Used in Environmental Protection:
Thifensulfuron is used as an environmentally friendly alternative to traditional herbicides. Its targeted action on specific weeds minimizes the impact on non-target plants and the surrounding ecosystem, promoting sustainable agricultural practices.
Used in Crop Protection:
Thifensulfuron is used as a crop protection agent to safeguard crops from the detrimental effects of weeds. By controlling weed growth, it helps in maintaining the health and productivity of the crops, ensuring a stable food supply.

79277-67-1

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79277-67-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79277-67-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,7 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79277-67:
(7*7)+(6*9)+(5*2)+(4*7)+(3*7)+(2*6)+(1*7)=181
181 % 10 = 1
So 79277-67-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H11N5O6S2/c1-5-12-9(15-11(13-5)22-2)14-10(19)16-24(20,21)6-3-4-23-7(6)8(17)18/h3-4H,1-2H3,(H,17,18)(H2,12,13,14,15,16,19)

79277-67-1SDS

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 thifensulfuron

1.2 Other means of identification

Product number -
Other names thiameturon

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:79277-67-1 SDS

79277-67-1Upstream product

79277-67-1Downstream Products

79277-67-1Relevant academic research and scientific papers

HERBICIDAL COMPOSITIONS

-

, (2022/03/02)

The present invention provides compositions comprising herbicidally active compounds (A) and (B), where (A) represents one or more compounds of the general formula (I) or agrochemically compatible salts thereof [component (A)], and (B) represents one or more herbicides [component (B)]. The application further relates to a method and to the use of the herbicidal composition according to the invention for controlling harmful plants or for regulating growth.

Rearrangement products in aqueous photolysis of thifensulfuron methyl

Sharma, Ashok K.,Ryan, David L.,Marr, Nina L.,Wadsley, Michael P.,Cheatham, Steve F.

, p. 401 - 410 (2017/06/29)

Photo-degradation of [14C]-thifensulfuron methyl has been investigated in aqueous media using a light source which simulates sunlight. Degradation of thifensulfuron methyl proceeds predominantly via sulfonylurea bridge ipso-contraction, and via cleavage of the bridge structure, to yield products in which the thiophene and the triazine rings have disconnected. One significant degradation product, which accounts for nearly 10%, retained both rings with truncated bridge moiety. Surprisingly, this product had thiophene ring substituents rearranged from their original locations. Other laboratories have reported photodegradation of thifensulfuron-methyl, and identified similar degradation products as well. The structure of the rearrangement product has been misidentified in previous reports because the rearrangement of the thiophene ring is not widely recognized. An unambiguous identification of this product and potential rearrangement mechanisms are presented in this report.

Herbicidal compositions with increased crop safety

-

, (2008/06/13)

Disclosed are herbicidal concentrate formulation compositions having reduced grass crop plant phytotoxicity comprising certain sulfonamide or sulfonylurea herbicides in admixture with a non-herbicidal organic or inorganic acid or mixture thereof in an amount sufficient to insure that during the post-emergent agricultural uses thereof in water diluted form the pH of the mixture is below about 5; also disclosed is the preparation of said compositions, aqueous formulations of said concentrate and the use of said formulations.

Herbicidal heterocyclic sulfonylurea compositions safened by herbicidal acids such as 2,4-D below a pH of 5

-

, (2008/06/13)

Disclosed are herbicidal concentrate formulation compositions having reduced grass crop plant phytotoxicity comprising certain sulfonamide or sulfonylurea herbicides in admixture with a herbicidal organic acid from the group consisting of clopyralid, 2,4-D, 2,4-DP, dicamba, dichlorprop-P, fluroxypyr MCPA, MCPP, mecoprop-P, picloram, triclopyr or mixtures of said acids; also disclosed is the preparation of said compositions and the pre- and post-emergent agricultural uses thereof in water diluted form.

Triazinyl-sulfonyl-ureas and isoureas

-

, (2008/06/13)

This invention relates to ureas and isoureas which are useful as herbicides and plant growth regulants. In particular, compounds of the instant invention have demonstrated great selectivity.

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