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TERT-BUTYL (3,6-DICHLOROPYRIDAZIN-4-YL)METHYLCARBAMATE is a chemical compound characterized by the presence of tert-butyl, 3,6-dichloropyridazin-4-yl, and methylcarbamate functional groups. It is recognized for its high efficacy in controlling pests and weeds, making it a valuable asset in agricultural applications.

631914-72-2

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631914-72-2 Usage

Uses

Used in Agricultural Industry:
TERT-BUTYL (3,6-DICHLOROPYRIDAZIN-4-YL)METHYLCARBAMATE is used as a pesticide or herbicide for its ability to effectively manage and control pests and weeds. It is valued for its targeted action on specific pests while maintaining relative safety for other plants and animals, thus contributing to crop protection and yield enhancement.
However, it is crucial to handle this chemical with care due to its potential health risks and environmental hazards if used improperly or exposed inappropriately. Proper application and safety measures are essential to mitigate any adverse effects and ensure the sustainability of agricultural practices.

Check Digit Verification of cas no

The CAS Registry Mumber 631914-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,1,9,1 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 631914-72:
(8*6)+(7*3)+(6*1)+(5*9)+(4*1)+(3*4)+(2*7)+(1*2)=152
152 % 10 = 2
So 631914-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13Cl2N3O2/c1-10(2,3)17-9(16)15(4)6-5-7(11)13-14-8(6)12/h5H,1-4H3

631914-72-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[(3,6-dichloropyridazin-4-yl)methyl]carbamate

1.2 Other means of identification

Product number -
Other names TERT-BUTYL (3,6-DICHLOROPYRIDAZIN-4-YL)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:631914-72-2 SDS

631914-72-2Downstream Products

631914-72-2Relevant academic research and scientific papers

MONOCYCLIC AGONISTS OF STIMULATOR OF INTERFERON GENES STING

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Paragraph 00119-00120, (2021/02/26)

The invention provides compounds having STimulator of INterferon Genes (STING) agonistic bioactivity that can be used in the treatment of tumors in patients afflicted therewith. The compounds are of formula (IA), formula (I), and formula (II): wherein the various substituents are as defined herein. Ring A is a 5- or 6- membered heteroaryl comprising 1, 2, or 3 N atoms, unsubstituted or substituted with 1, 2, or 3 groups as defined herein. Compounds for practice of a method of the invention can be delivered via oral delivery for systemic exposure, as well as delivered intratumorally. Antitumor therapy using a compound of formula (I) can further comprise administration of an effective dose of an immunecheckpoint targeting drug.

CYCLOPROPANE DERIVATIVE AND DRUG CONTAINING SAME

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Paragraph 0162, (2018/06/15)

A compound represented by the formula (I): wherein each symbol is as defined in the DESCRIPTION, or a pharmaceutically acceptable salt thereof has superior TRPA1 antagonist activity, and the compound or a pharmaceutically acceptable salt thereof is useful for the prophylaxis or treatment of diseases involving TRPA1 antagonist and TRPA1.

HETEROCYCLIC SULFONAMIDE DERIVATIVE AND MEDICINE COMPRISING SAME

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Paragraph 0605; 0614; 0615, (2016/12/01)

The present invention provides a compound represented by the formula (I): wherein each symbol is as defined in the DESCRIPTION, or a pharmaceutically acceptable salt thereof. The compound has a superior TRPA1 antagonist activity, and can provide a medicament useful for the prophylaxis or treatment of diseases involving TRPA1 antagonist and TRPA1.

Use of N-Protected Amino Acids in the Minisci Radical Alkylation

Cowden, Cameron J.

, p. 4497 - 4499 (2007/10/03)

(Equation presented) The Minisci radical alkylation has been demonstrated on a range of commercially available glycine derivatives and proceeds in good to high yield. When extending the reaction to other amino acids, competitive oxidation of the initially formed radical was overcome by using the phthalimide protecting group.

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