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3-Chloro-6-benzyloxypyridazine, an organic compound with the chemical formula C12H9ClN2O, is a member of the pyridazine family. It is characterized by the presence of a chlorine atom at the 3-position and a benzyloxy group at the 6-position on the pyridazine ring. 3-CHLORO-6-BENZYLOXYPYRIDAZINE is known for its potential in creating heterocyclic compounds with a range of biological activities, making it a valuable component in the development of pharmaceuticals and agrochemicals.

91063-19-3

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91063-19-3 Usage

Uses

Used in Pharmaceutical Synthesis:
3-Chloro-6-benzyloxypyridazine is utilized as a key intermediate in the synthesis of pharmaceuticals. Its unique structural features allow for the development of heterocyclic compounds with diverse biological activities, contributing to the creation of new drugs with potential therapeutic benefits.
Used in Agrochemical Production:
In the agrochemical industry, 3-chloro-6-benzyloxypyridazine serves as a building block for the production of various compounds with applications in agriculture. Its ability to form heterocyclic compounds with different biological properties makes it a valuable asset in the development of new agrochemicals aimed at enhancing crop protection and productivity.
Used in Organic Synthesis:
3-Chloro-6-benzyloxypyridazine is also employed as a versatile building block in organic synthesis. Its structural features enable the production of a wide range of compounds with medicinal and agricultural applications, further expanding its utility in the fields of chemistry and material science.
Ongoing Research and Development:
Due to its potential applications and structural features, 3-chloro-6-benzyloxypyridazine is the subject of ongoing research and development in the fields of chemistry, pharmaceuticals, and agrochemicals. Scientists and researchers are continually exploring new ways to harness its properties and expand its uses in creating innovative solutions for various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 91063-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,6 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91063-19:
(7*9)+(6*1)+(5*0)+(4*6)+(3*3)+(2*1)+(1*9)=113
113 % 10 = 3
So 91063-19-3 is a valid CAS Registry Number.

91063-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Benzyloxy)-6-chloropyridazine

1.2 Other means of identification

Product number -
Other names 3-chloro-6-phenylmethoxypyridazine

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:91063-19-3 SDS

91063-19-3Relevant articles and documents

2-HETEROARYL-PYRROLO [3,4-C]PYRROLE DERIVATIVES, AND USE THEREOF AS SCD INHIBITORS

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Page/Page column 20, (2012/02/06)

The invention relates to compounds of the formula (I), where the groups R1, M, A, B, D, L, and R have the specified meanings, and to the physiologically compatible salts thereof. The compounds are suitable, for example, for treating metabolic syndrome, in

(HETERO)ARYL COMPOUNDS WITH MCH ANTAGONISTIC ACTIVITY AND MEDICAMENTS COMPRISING THESE COMPOUNDS

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Page/Page column 79, (2010/11/27)

The present invention relates to (hetero)aryl compounds of general formula (I) wherein the groups and radicals A, B, Q, W, X, Y, Z, R1, R2, R4a, R4b, R5a, R5b, have the meanings given in cl

Sulfonyl pyridazinone compounds useful as aldose reductase inhibitors

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, (2008/06/13)

This invention relates to novel sulfonyl pyridazinone compounds useful as aldose reductase inhibitors in the treatment or prevention of certain complications arising from diabetes mellitus, pharmaceutical compositions comprising the sulfonyl pyridazinone, pharmaceutical compositions comprising a combination of the sulfonyl pyridazinone together with a second pharmaceutical agent, therapeutic methods comprising the administration of the sulfonyl pyridazinone compounds, therapeutic methods comprising the administration of the sulfonyl pyridazinone compounds in combination with a second pharmaceutical agent and compounds useful as intermediates for preparing the sulfonyl pyridazinone compounds of this invention.

Therapies for tissue damage resulting from ischemia

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, (2008/06/13)

This invention relates to therapeutic methods for treatment or prevention of tissue damage resulting from ischemia in mammals.

Sulfonyl pyridazinone compounds useful as aldose reductase inhibitors

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Page 28, (2010/01/31)

Compounds of the formula (I): a prodrug thereof or a pharmaceutically acceptable salt of said compound or said prodrug, wherein R1, R2, X and Y are as defined in the claims are aldose reductase inhibitors useful in the treatment or p

Pyridazinone aldose reductase inhibitors

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, (2008/06/13)

The present invention relates to novel pyridazinone compounds, pharmaceutical compositions comprising those compounds and to methods of using such compounds and compositions to inhibit aldose reductase, lower sorbitol levels and, thus, lower fructose levels, and/or treat or prevent diabetic complications such as diabetic neuropathy, diabetic retinopathy, diabetic nephropathy, diabetic cardiomyopathy, diabetic microangiopathy and diabetic macroangiopathy in mammals. This invention also relates to methods of affording cardioprotection to subjects not suffering from diabetes. This invention also relates to pharmaceutical compositions and kits comprising a combination of an aldose reductase inhibitor (ARI) of this invention and a sorbitol dehydrogenase inhibitor and to methods of using such compositions or kits to treat or prevent the above diabetic complications in mammals. This invention also relates to other combinations with the ARIs of this invention, including combinations with adendsine agonists; NHE-1 inhibitors; glycogen phosphorylase inhibitors; selective serotonin reuptake inhibitors; GABA agonists; antihypertensive agents; 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors; phosphodiesterase-5 inhibitors; and to glucose lowering agents.

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